WO2004009622A2

WO2004009622A2 - Protein complexes of cellular networks underlying the development of cancer and other diseases

Info

Publication number: WO2004009622A2
Application number: PCT/EP2003/007835
Authority: WO
Inventors: Alejandro Merino; Tewis Bouwmeester; Andreas Bauer; Gerard Drewes; Martina Marzioch; Ulrich Kruse; Giulio Superti-Furga; Dirk Eberhard; Heinz Ruffner; Scott Hobson; Gerd Helftenbein; Cristina Cruciat
Original assignee: Cellzome Ag
Priority date: 2002-07-19
Filing date: 2003-07-18
Publication date: 2004-01-29
Also published as: AU2003281515A1; WO2004009622A3

Abstract

The present invention relates to protein complexes involved in cellular processes which have been shown to be critical for the development of various forms of cancer, component proteins of the said complexes, fragments and derivatives of the component proteins, and antibodies specific to the complexes. The present invention also relates to methods for use of the complexes and their interacting proteins in, inter alia, screening, diagnosis, and therapy, as well as to methods of preparing the complexes.

Description

PROTEIN COMPLEXES OF CELLULAR NETWORKS UNDERLYING THE DEVELOPMENT OF CANCER AND OTHER DISEASES

1. FIELD OF THE INVENTION

2. BACKGROUND OF THE INVENTION

Despite enormous efforts, cancer still remains as one of the major types of diseases affecting humans.Although significant progress has been made in the development of therapies, the situation in the cancer field in general, an urgent need for new therapies, i.e. new medicaments exists. To progress, a better understanding of the molecular mechanisms is necessary, serving as a basis for a directed identification of suitable drug targets. To further address the biological context of proteins which have been identified to be key players in the development of several cancers, protein interactors were searched for. By applying a novel approach, it was shown that the proteins, rather then interacting with individual proteins, form aggregations which could also be described as "protein complexes". The proteins which have been analysed as being key players in processes underlying the development of cancer are further described below.

Pot1

In all eukaryotic species the ends of chromosomes have specialized non-coding DNA squences that, together with associated proteins, are known as telomers. Telomeres act as protective caps, preventing both degradation of the ends of chromosomes and their recognition as double-strand breaks, which otherwise would result in aberrant recombination. Telomeric DNA consists of simple tandem repeats of guanine-rich sequences (hexanucleotide repeats d(TTAGGG) in vertebrates). The extreme 3' end is single stranded and typically 100-200 bases long. It is extensively associated with a variety of proteins. One of them is the Pot1 protein (protection of telomeres) which was described in fission yeast and humans.

However, despite various lines of evidence were presented so far, the full biological context of Pot1 and thus, the role of the proteins associated with Pot1 in the cell and particularly in pathogenic conditions have remained largely elusive.

Her2

Growth factors and their transmembrane receptor tyrosine kinases play important roles in cell proliferation, survival, migration and differentiation. One group of growth factors, comprising epidermal growth factor (EGF)-like proteins and neuregulins, stimulates cells to divide by activating members of the EGF receptor (EGFR) family, which consists of the EGFR itself and the receptors known as HER2-4. Her receptors exist as monomers but dimerize on ligand binding. No Her2-specific ligand has been identified but Her2 is the preferred heterodimerization partner for other Her receptors. Amplification of the Her2 gene or overexpression of the Her2 protein is associated with malignancy and a poor prognosis in breast cancer.

Thus, despite various lines of evidence were presented so far, the full biological context of Her2 and thus, the role of the proteins associated with Her2 in the cell and particularly in pathogenic conditions have remained largely elusive.

Rinqol

Cyclin-dependent kinases (Cdks) are essential regulators of the eukaryotic cell division cycle. Cdks are subject to many modes and levels of regulation in response to both intracellular and extracellular signals. They are activated through their association with regulatory subunits called cyclins that are synthesized and degraded in a cell cycle- dependent manner. CDK-cyclin complexes are in turn regulated by the cyclin-dependent kinase inhibitors (CDKls), which generally inhibit cell cycle progression. Recently it has been shown that Cdk1 (Cdc2) and Cdk2 can also be activated by a protein called Ringo. Ringo has no similarity to cyclins at the amino acid sequence level. Cdk-Ringo complexes may be active under conditions in which cyclin-bound Cdks are inhibited and therefore play different regulatory roles. Thus, despite various lines of evidence were presented so far, the full biological context of Ringo and thus, the role of the proteins associated with Ringo in the cell and particularly in pathogenic conditions have remained largely elusive.

Gab1

The GAB1 complex plays an important role in various cytokines, growth factors, and antigen receptors signaling. Several signaling molecules, such as MET (HGFR), EGFR, SHP2, PI 3-kinase, GRB2, SHIP2, SHC, SOS, PLC gamma, and CRK, have been found associated directly or indirectly with GAB1. GAB1 is expressed in all tissues examined except liver, lung, and kidney. The larger splice variant was cloned and used in this experiment as a entry point of retrieval. We have seen, that complex formation is mediated via tyrosine phosphorylation of GAB1 (data available in a separate document). Upon induction of tyrosine phosphorylation with vanadate as well as HGF, we have identified most of the known interactor, validating our findings, as well as several novel components that include, detailed below that may influence GAB1 activity and play important roles in proliferation and metastatic signaling. We have also identified several novel interactors in the absence of tyrosine phosphorylation that could be sequestered by GAB1 to keep them inactive.

However, despite various lines of evidence were presented so far, the full biological context of Gab1 and thus, the role of the proteins associated with Gab1 in the cell and particularly in pathogenic conditions have remained largely elusive.

Bcl2

Bcl-2 family proteins are key regulators of programmed cell death. The Bcl-2 family includes both anti- and pro-apoptotic proteins with opposing biological functions in either inhibiting or promoting cell death. High expression of anti-apoptotic members such as Bcl-2 and Bcl-XL commonly found in human cancers contributes to neoplastic cell expansion and interferes with the therapeutic action of many chemotherapeutic drugs. The functional blockade of Bcl-2 or Bcl-XL could either restore the apoptotic process in tumor cells or sensitize these tumors for chemo- and radiotherapies. Thus, despite various lines of evidence were presented so far, the full biological context of Bcl-2 and thus, the role of the proteins associated with Bcl-2 in the cell and particularly in pathogenic conditions have remained largely elusive.

3. SUMMARY OF THE INVENTION

An object of the present invention was to identify protein complexes formed around protein which have been shown to be critical for the development of various forms of cancer, component proteins of the said complexes, fragments and derivatives of the component proteins, and antibodies specific to the complexes. The present invention also relates to methods for use of these proteins and their interacting proteins in, inter alia, screening, diagnosis, and therapy, as well as to methods of preparing the complexes.

By applying the process according to the invention said complexes were identified. The components are listed in table 1.

Said object is further achieved by the characterization of component proteins. These proteins are listed in table 2.

Thus, the invention relates to the following embodiments:

1. A protein complex selected from complex (I) and comprising

(a) at least one first protein, which first protein is selected from the group of proteins in table 1 , fourth column of a given complex, or a functionally active derivative thereof, or a functionally active fragment thereof, or a homologue thereof, or a variant of said protein, the variant being encoded by a nucleic acid that hybridizes to the nucleic acid encoding said protein under low stringency conditions; and

(b) at least one second protein, which second protein is selected from the group of proteins in table 1 , fifth column of said given complex, or a functionally active derivative thereof, or a functionally active fragment thereof, or a homologue thereof, or a variant of said second protein, said variant being encoded by a nucleic acid that hybridizes to the nucleic acid encoding said protein under low stringency conditions; and a complex (II) comprising at least two of said second proteins, wherein said low stringency conditions comprise hybridization in a buffer comprising 35% formamide, 5X SSC, 50 mM Tris-HCI (pH 7.5), 5 mM EDTA, 0.02% PVP, 0.02% BSA, 100 ug/ml denatured salmon sperm DNA, and 10% (wt/vol) dextran sulfate for 18-20 hours at 40°C, washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4), 5 mM EDTA, and 0.1% SDS for 1-5 hours at 55°C, and washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4) 5 mM EDTA, and 0.1% SDS for 1.5 hours at 60°C.

2. A protein complex comprising a first protein selected from the proteins listed in table 1 , fourth column of a given complex or a homologue or variant thereof, or a functionally active fragment or functionally active derivative of said first protein, the variant being encoded by a nucleic acid that hybridizes to the nucleic acid of said first protein under low stringency conditions, and at least one second protein selected from the group of proteins in table 1 , fifth column of a given complex, or a variant or homologue thereof, or a functionally active fragment or a functionally active derivative of said second protein, the variant of said second protein being encoded by a nucleic acid that hybridizes to the nucleic acid of said second protein under low- stringency conditions, and wherein said low stringency conditions comprise hybridization in a buffer comprising 35% formamide, 5X SSC, 50 mM Tris-HCI (pH

^• 7.5), 5 mM EDTA, 0.02% PVP, 0.02% BSA, 100 ug/ml denatured salmon sperm DNA, and 10% (wt/vol) dextran sulfate for 18-20 hours at 40°C, washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4), 5 mM EDTA, and 0.1% SDS for 1-5 hours at 55°C, and washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4) 5 mM EDTA, and 0.1% SDS for 1.5 hours at 60°C.

3. A protein complex comprising all proteins selected from the proteins in table 1 , third column of a given complex or at least one protein being a homologue thereof, or a variant thereof or functionally active fragment or functionally active derivative of said protein, said variant being encoded by a nucleic acid that hybridizes to the nucleic acid of said protein under low stringency conditions; wherein said low stringency conditions comprise hybridization in a buffer comprising 35% formamide, 5X SSC, 50 mM Tris-HCI (pH 7.5), 5 mM EDTA, 0.02% PVP, 0.02% Ficoll, 0.2% BSA, 100 ug/ml denatured salmon sperm DNA, and 10% (wt/vol) dextran sulfate for 18-20 hours at 40°C, washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4), 5 mM EDTA, and 0.1 % SDS for 1-5 hours at 55°C, and washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4), 5 mM EDTA, and 0.1% SDS for 1.5 hours at 60°C.

4. A protein complex that comprises all proteins as listed in table 1 , third column for a given complex or at least one protein being a homologue or a variant thereof, or a functionally active fragment or a functionally active derivative thereof, the variant being encoded by a nucleic acid that hybridizes to the nucleic acid of any of said proteins under low stringency conditions, except at least one protein of the proteins listed in table 5, third column, wherein said low stringency conditions compπse hybridization in a buffer comprising 35% formamide, 5X SSC, 50 mM Tris-HCI (pH 7.5), 5 mM EDTA, 0.02% PVP, 0.02% Ficoll, 0.2% BSA, 100 ug/ml denatured salmon sperm DNA, and 10% (wt/vol) dextran sulfate for 18-20 hours at 40°C, washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4), 5 mM EDTA, and 0.1% SDS for 1-5 hours at 55°C, and washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4), 5 mM EDTA, and 0.1% SDS for 1.5 hours at 60°C, with the provisio that the complex comprises at least one protein selected from table 1 , fifth column of a given complex.

5. The complex of any of No. 1 - 4 comprising at least one functionally active derivative of said first protein and/or a functionally active derivative of said second protein, wherein the functionally active derivative is a fusion protein comprising said first protein or said second protein fused to an amino acid sequence different from the first protein or second protein.

6. The complex of No. 5 wherein the functionally active derivative is a fusion protein comprising said first protein or said second protein fused to an affinity tag or label.

7. The complex of any of No. 1 - 4 comprising a fragment of said first protein and/or a fragment of said second protein, which fragment binds to another protein component of said complex.

8. The complex of any of No. 1 - 7 that is involved in at least one biochemical activity as stated in table 3. 9. A process for preparing a complex of any of No. 1 - 8 and optionally the components thereof comprising the following steps: expressing a protein of the complex, preferably a tagged protein, in a target cell, or a tissue or an organ, isolating the protein complex which is attached to the protein, preferably the tagged protein, and optionally disassociating the protein complex and isolating the individual complex members.

10. The process according to No. 9 wherein the tagged protein comprises two different tags which allow two separate affinity purification steps.

11. The process according to any of No. 9 - 10 wherein the two tags are separated by a cleavage site for a protease.

12. Component of a protein complex obtainable by a process according to any of No. 9 - 11.

13. Protein selected from the group of proteins in table 1 , sixth column of a given complex or a homologue or a variant of thereof, or a functionally active fragment or a functionally active derivative of said protein, the variant being encoded by a nucleic acid that hybridizes to the nucleic acid encoding said protein under low stringency conditions, wherein said low stringency conditions comprise hybridization in a buffer compπsing 35% formamide, 5X SSC, 50 mM Tris-HCI (pH 7.5), 5 mM EDTA, 0.02% PVP, 0.02% Ficoll, 0.2% BSA, 100 ug/ml denatured salmon sperm DNA, and 10% (wt/vol) dextran sulfate for 18-20 hours at 40°C, washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4), 5 mM EDTA, and 0.1 % SDS for 1.5 hours at 55°C, and washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4), 5 mM EDTA, and 0.1% SDS for 1.5 hours at 60°C.

14. Nucleic acid encoding a protein according to No. 13.

15. Construct, preferably a vector construct, comprising

(a) a nucleic acid according to No. 14 and at least one further nucleic acid which is normally not associated with said nucleic acid, or (b) at least two separate nucleic acid sequences each encoding a different protein, or a functionally active fragment or a functionally active derivative thereof, or a homologue or a variant thereof, at least one of said proteins being selected from the first group of proteins according to No. 1 (a) and at least one of said proteins, being selected from the second group of proteins according to No. 1 (b) or

(c) at least two separate nucleic acid sequences each encoding a different protein, or a functionally active fragment or a functionally active derivative thereof, or a homologue or a variant thereof, said proteins being selected from the proteins of complex (II) according to No. 1.

16. Host cell, containing a vector comprising at least one nucleic acid of No. 14 and /or a construct of No. 15 or containing several vectors each comprising at least one nucleic acid encoding at least one protein selected from the first group of proteins according to No. 1 (a) and at least one nucleic acid encoding at least one protein selected from the second group of proteins according to No. 1 (b).

17. An antibody or a fragment of said antibody containing the binding domain thereof, selected from an antibody or fragment thereof, which binds the complex of any of No. 1 - 8 and which does not bind any of the proteins of said complex when uncomplexed and an antibody or a fragment of said antibody containing the binding domain thereof which binds to any of the proteins of the group of proteins according to No. 13.

18. A kit comprising in one or more containers:

(a) the complex of any of No. 1 - 8 and/or the proteins of No. 13 and/or

(b) an antibody according to No. 17 and/or

(c) a nucleic acid encoding a protein of the complex of any of No. 1 - 8 and/or a protein of No. 13 and/or

(d) cells expressing the complex of any of No. 1 - 8 and/or a protein of No. 13 and, optionally,

(e) further components such as reagents, buffers and working instructions.

19. The kit according to No. 18 for processing a substrate of a complex of any one of No. 20. The kit according to No. 18 for the diagnosis or prognosis of a disease or a disease risk, preferentially for a disease or disorder such as those as stated in column 2, table 4 of a given complex.

21. Array, preferably a microarray, in which at least a complex according to any of No. 1 - 8 and/or at least one protein according to No. 13 and/or at least one antibody according to No. 17 is attached to a solid carrier.

22. A process for modifying a substrate of a complex of any one of No. 1 - 8 comprising the step of bringing into contact a complex of any of No. 1 - 8 with said substrate, such that said substrate is modified.

23. A pharmaceutical composition comprising the protein complex of any of No. 1 - 8 and/or a protein according to No. 13.

24. A pharmaceutical composition according to No. 23 for the treatment of diseases and disorders, preferentially for diseases or disorders such as those as stated in column 2, table 4 of a given complex.

25. A method for screening for a molecule that binds to a complex of any one of No. 1 - 8 and/or a protein of No. 13, comprising the following steps:

(a) exposing said complex or protein, or a cell or organism containing said complex or said protein, to one or more candidate molecules; and

(b) determining whether said candidate molecule is bound to the complex or protein.

26. A method for screening for a molecule that modulates directly or indirectly the function, activity, composition or formation of a complex of any one of No. 1 - 8 comprising the steps of:

(a) exposing said complex, or a cell or organism containing said complex to one or more candidate molecules; and

(b) determining the amount of, activity of, protein components of, and/or intracellular localization of, said complex and/or the transcription level of a gene regulated by the complex and/or the abundance and/or activity of a protein or protein complex dependent upon the function of the complex and/or product of a gene dependent on the complex in the presence of the one or more candidate molecules, wherein a change in said amount, activity, protein components or intracellular localization relative to said amount, activity, protein components and/or intracellular localization and/or a change in the transcription level of a gene regulated by the complex and/or the abundance and/or activity of a protein or protein complex dependent on the function of the complex and/or product of a gene dependent on the complex in the absence of said candidate molecules indicates that the molecule modulates function, activity, or composition of said complex.

27. The method of No. 26, wherein the amount of said complex is determined.

28. The method of No. 26, wherein the activity of said complex is determined.

29. The method of No. 28, wherein said determining step comprises isolating from the cell or organism said complex to produce said isolated complex and contacting said isolated complex in the presence or absence of a candidate molecule with a substrate of said complex and determining whether said substrate is processed in the absence of the candidate molecule and whether the processing of said substrate is modified in the presence of said candidate molecule.

30. The method of No. 26, wherein the amount of the individual protein components of said complex is determined.

31. The method of No. 30, wherein said determining step comprises determining whether any of the proteins listed in table 1 , third column of said complex, or a functionally active fragment or a functionally active derivative thereof, or a variant or a homologue thereof, the variant being encoded by a nucleic acid that hybridizes to the nucleic acid of said protein under low-stringency conditions, is present in the complex.

32. The method of any of No. 26 - 31 , wherein said method is a method of screening for a drug for treatment or prevention of a disease or disorder, preferentially of a disease or disorder selected from the diseases or disorders such as those as stated in column 2, table 4 of a given complex. 33. Use of a molecule that modulates the amount of, activity of, or the protein components of the complex of any one of No. 1 - 8 for the manufacture of a medicament for the treatment or prevention of a disease or disorder, preferentially of a disease or disorder such as those as stated in column 2, table 4 of a given complex.

34. A method for the production of a pharmaceutical composition comprising carrying out the method of No. 26 - 31 to identify a molecule that modulates the function, activity, composition or formation of said complex, and further comprising mixing the identified molecule with a pharmaceutically acceptable carrier.

35. A method for diagnosing or screening for the presence of a disease or disorder or a predisposition for developing a disease or disorder in a subject, which disease or disorder is characterized by an aberrant amount of, component disposition of, or intracellular localization of the complex of any one of the No. 1 - 8, comprising determining the amount of, activity of, protein components of, and/or intracellular localization of, said complex and/or the transcription level of a gene regulated by the complex and/or the abundance and/or activity of a protein or protein complex dependent on the function of the complex and/or product of a gene dependent on the complex in a comparative sample derived from a subject, wherein a difference in said amount, activity, or protein components of, said complex in a corresponding sample from a subject not having the disease or disorder or predisposition indicated the presence in the subject of the disease or disorder or predisposition in the subject.

36. The method of No. 35, wherein the amount of said complex is determined.

37. The method of No. 35, wherein the activity of said complex is determined.

38. The method of No. 37, wherein said determining step comprises isolating from the cell or organism said complex to produce said isolated complex and contacting said isolated complex in the presence or absence of a candidate molecule with a substrate of said complex and determining whether said substrate is processed in the absence of the candidate molecule and whether the processing of said substrate is modified in the presence of said candidate molecule.

39. The method of No. 35, wherein the amount of the individual protein components of said complex is determined.

40. The method of No. 39, wherein said determining step comprises determining whether any of the proteins according to No. 13 is present in the complex.

41. The complex of any one of No. 1 - 8, or a protein of No. 13 or an antibody or fragment thereof of No. 17, for use in a method of diagnosing a disease or disorder, preferentially of a disease or disorder such as neurodegenerative disease such as those as stated in column 2, table 4 of a given complex.

42. A method for treating or preventing a disease or disorder characterized by an aberrant amount of, activity of, component composition of or intracellular localization of, the complex of any one of No. 1 - 8, comprising administering to a subject in need of such treatment or prevention a therapeutically effective amount of one or more molecules that modulate the amount of, activity of, or protein composition of, said complex.

43. The method according to No. 42, wherein said disease or disorder involves decreased levels of the amount or activity of said complex.

44. The method according to No. 42, wherein said disease or disorder involves increased levels of the amount or activity of said complex.

45. Complex of No. 1 - 8 and/or a protein as listed in table 1 , fifth column of said complex as a target for an active agent of a pharmaceutical, preferably a drug target, in the treatment or prevention of a disease or disorder, preferentially of a disease or disorder such as a neurodegenerative disease such as those as stated in column 2, table 4 of a given complex.

3.1 DEFINITIONS The term "activity" as used herein, refers to the function of a molecule in its broadest sense. It generally includes, but is not limited to, biological, biochemical, physical or chemical functions of the molecule. It includes for example the enzymatic activity, the ability to interact with other molecules and ability to activate, facilitate, stabilize, inhibit, suppress or destabilize the function of other molecules, stability, ability to localize to certain subcellular locations. Where applicable, said term also relates to the function of a protein complex in its broadest sense.

The term "agonist" as used herein, means a molecule which modulates the formation of a protein complex or which, when bound to a complex or protein of the invention or a molecule in the protein complex, increases the amount of, or prolongs the duration of, the activity of the complex. The stimulation may be direct or indirect, including effects on the expression of a gene encoding a member of the protein complex, or by a competitive or non-competitive mechanism. Agonists may include proteins, nucleic acids, carbohydrates or any other organic or anorganic molecule or metals. Agonists also include a functional peptide or peptide fragment derived from a protein member of the complexes of the invention or a protein member itself of the complexes of the invention.' Preferred activators are those which, when added to the complex and/or the protein of the invention under physiological conditions and/or in vitro assays, including diagnostic or prognostic assays, result in a change of the level of any of the activities of the protein complex and/or the proteins of the invention as exemplary illustrated above by at least 10%, at least 25%, at least 50%, at least 100%, at least, 200%, at least 500% or at least 1000% at a concentration of the activator 1μg ml^"1, 10 /g ml^"1, 100μg ml^"1, 500 /g ml^"1, 1 mg ml^"1, 10mg ml^"1 or 100mg ml^"1. Any combination of the above mentioned degrees of percentages and concentration may be used to define an agonist of the invention, with greater effect at lower concentrations being preferred.

The term "amount" as used herein and as applicable to the embodiment described relates to the amount of the particular protein or protein complex described, including the value of null, i.e. where no protein or protein complex described in that particular embodiment is present under the or any of the conditions which might be specified in that particular embodiment.

The term "animal" as used herein includes, but is not limited to mammals, preferably mammals such as cows, pigs, horses, mice, rats, cats, dogs, sheep, goats and most preferably humans. Other animals used in agriculture, such as chickens, ducks etc. are also included in the definition as used herein.

The term "animal" as used herein does not include humans if being used in the context of genetic alterations to the germline.

The term "antagonist" as used herein, means a molecule which modulates the formation of a protein complex or which, when bound to a complex or protein of the invention or a molecule in the protein complex, decreases the amount of, or the duration or level of activity of the complex. The effect may be direct or indirect, including effects on the expression of a gene encoding a member of the protein complex, or by a competitive or non-competitive mechanism. Antagonists may include proteins, including antibodies, nucleic acids, carbohydrates or any other organic or anorganic molecule or metals. Antagonists also include a functional peptide or peptide fragment derived from a protein member of the complexes of the invention or a protein member itself of the complexes of the invention. Preferred antagonists are those which, when added to the complex and/or the protein of the invention under physiological conditions and/or in vitro assays, including diagnostic or prognostic assays, result in a change of the level of any of the activities of the protein complex and/or the proteins of the invention as exemplary illustrated above by at least 10%, at least 20%, at least 30%, at ieast 40% at least 50%, at least 60%, at least 70%, at least 80%, at least 90%, at least 95% or at least 99% at a concentration of the inhibitor of 1μg ml^"1, 10μg ml^"1, 100μg ml^"1, 500μg ml^'1, 1mg ml^"1, 10mg ml^"1 or 100mg ml^"1.

Any combination of the above mentioned degrees of percentages and concentration may be used to define antagonist of the invention, with greater effect at lower concentrations being preferred.

The term "antibodies" as used herein, include include, but are not limited to, polyclonal, monoclonal, chimeric, single chain, Fab fragments, and an Fab expression library.

The term "binding" as used herein means a stable or transient association between two molecules, including electrostatic, hydrophobic, ionic and/or hydrogen-bond interaction under physiological conditions and/or conditions being used in diagnostic or prognostic method or process or procedure.

The term "carrier" as used herein refers to a diluent, adjuvant, excipient, or vehicle with which the therapeutic is administered. Such pharmaceutical carriers can be sterile liquids, such as water and oils, including those of petroleum, animal, vegetable or synthetic origin, including but not limited to peanut oil, soybean oil, mineral oil, sesame oil and the like. Water is a preferred carrier when the pharmaceutical composition is administered orally. Saline and aqueous dextrose are preferred carriers when the pharmaceutical composition is administered intravenously. Saline solutions and aqueous dextrose and glycerol solutions are preferably employed as liquid carriers for injectable solutions. Suitable pharmaceutical excipients include starch, glucose, lactose, sucrose, gelatin, malt, rice, flour, chalk, silica gel, sodium stearate, glycerol monostearate, talc, sodium chloride, dried skim milk, glycerol, propylene, glycol, water, ethanol and the like. The composition, if desired, can also contain minor amounts of wetting or emulsifying agents, or pH buffering agents. These compositions can take the form of solutions, suspensions, emulsions, tablets, pills, capsules, powders, sustained-release formulations and the like. The composition can be formulated as a suppository, with traditional binders and carriers such as triglyceπ^'des. Oral formulation can include standard carriers such as pharmaceutical grades of mannitol, lactose, starch, magnesium stearate, sodium saccharine, cellulose, magnesium carbonate, etc. Examples of suitable pharmaceutical carriers are described in "Remington's Pharmaceutical Sciences" by E.W. Martin. Such compositions will contain a therapeutically effective amount of the therapeutic, preferably in purified form, together with a suitable amount of carrier so as to provide the form for proper administration to the patient. The formulation should suit the mode of administration..

If not stated otherwise, the terms "complex" and "protein complex" are used interchangeably herein and refer to a complex of proteins that is able to perform one or more functions of the wild type protein complex. The protein complex may or may not include and/or be associated with other molecules such as nucleic acid, such as RNA or DNA, or lipids or further cofactors or moieties selected from a metal ions, hormones, second messengers, phosphate, sugars.

A "complex" of the invention may also be part of or a unit of a larger physiological protein assembly.

The term "Telomere Capping Protein Complex" as used herein relates to the complexes of the invention formed around the protein Pot1.

The term "Her2-protein complex" as used herein relates to the complexes of the invention formed around the protein Her2.

The term "Ringol -protein complex" as used herein relates to the complexes of the invention formed around the protein Ringol . The term "Gab1 signalling protein complex" as used herein relates to the complexes of the invention formed around the protein Gab1.

The term "Bcl2-protein complex" as used herein relates to the complexes of the invention formed around the protein Bcl2.

If not stated otherwise, the term "compound" as used herein are include but are not limited to peptides, nucleic acids, carbohydrates, natural product extract librariesorganic molecules, preferentially small organic molecules, anorganic molecules, including but not limited to chemicals, metals and organometallic molecules.

The terms "derivatives" or "analogs of component proteins" or "variants" as used herein include, but are not limited, to molecules comprising regions that are substantially homologous to the component proteins, in various embodiments, by at least 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95% or 99% identity over an amino acid sequence of identical size or when compared to an aligned sequence in which the alignment is done by a computer homology program known in the art, or whose encoding nucleic acid is capable of hybridizing to a sequence encoding the component protein under stringent, moderately stringent, or nonstringent conditions. It means a protein which is the outcome of a modification of the naturally occurring protein, by amino acid substitutions, deletions and additios, respectively, which derivatives still exhibit the biological function of the naturally occurring protein although not necessarily to the same degree. The biological function of such proteins can e.g. be examined by suitable available in vitro assays as provided in the invention.

The term "functionally active" as used herein refers to a polypeptide, namely a fragment or derivative, having structural, regulatory, or biochemical functions of the protein according to the embodiment of which this polypeptide, namely fragment or derivative is related to.

The term "fragment" as used herein refers to a polypeptide of at least 10, 20, 30, 40 or 50 amino acids of the component protein according to the embodiment. In specific embodiments, such fragments are not larger than 35, 100 or 200 amino acids.

The term "gene" as used herein refers to a nucleic acid comprising an open reading frame encoding a polypeptide of, if not stated otherwise, the present invention, including both exon and optionally intron sequences.

The terms " homologue" or "homologous gene products" as used herein mean a protein in another species, preferably mammals, which performs the same biological function as the a protein component of the complex further described herein. Such homologues are also termed "orthologous gene products". The algorithm for the detection of orthologue gene pairs from humans and mammalians or other species uses the whole genome of these organisms. First, pairwise best hits are retrieved, using a full Smith-Waterman alignment of predicted proteins. To further improve reliability, these pairs are clustered with pairwise best hits involving Drosophila melanogaster and C. elegans proteins. Such analysis is given, e.g., in Nature, 2001 , 409:860-921. The homologues of the proteins according to the invention can either be isolated based on the sequence homology of the genes encoding the proteins provided herein to the genes of other species by cloning the respective gene applying conventional technology and expressing the protein from such gene, or by isolating proteins of the other species by isolating the analogous complex according to the methods provided herein or to other suitable methods commonly known in the art.

The term "host cells" or, were applicable, "cells" or "hosts" as used herein is intended to be understood in a broadest sense and include, but are not limited to mammalian cell systems infected with virus (e.g., vaccinia virus, adenovirus, etc.); insect cell systems infected with virus (e.g., baculovirus); microorganisms such as yeast containing yeast vectors; or bacteria transformed with bacteriophage, DNA, plasmid DNA, or cosmid DNA. The expression elements of vectors vary in their strengths and specificities. Depending on the host-vector system utilized, any one of a number of suitable transcription and translation elements may be used. It is understood that this term not only refers to the particular subject cell but to the progeny or potential progeny of such a cell. Because certain modifications may occur in succeeding generations due to either mutation of environmental influences, such progeny may not, in fact, be identical to the parent cell, but are still included within the scope of the term as used herein.

The term "modification" as used herein refers to all modifications of a protein or protein complex of the invention including cleavage and addition or removal of a group.

The term "nuleic acid" as used herein refers to polynucleotides such as deoxyribonucleic acid (DNA), and, where appropriate, ribonucleic acid (RNA). They may also be polynucleotides which include within them synthetic or modified nucleotides. A number of different types of modification to polynucleotides are known in the art. These include methylphosphonate and phosphorothioate backbones, addition of acridine or polylysine chains at the 3' and/or 5' ends of the molecule. For the purposes of the present invention, it is to be understood that the polynucleotides described herein may be modified by any method available in the art. Such modifications may be carried out in order to enhance the in vivo activity or lifespan of polynucleotides of the invention. Polynucleotides according to the invention may be produced recombinantly, synthetically, or by any means available to those of skill in the art. They may also be cloned by standard techniques. The polynucleotides are typically provided in isolated and/or purified form. As applicable to the embodiment being described, they include both single stranded and double-stranded polynucleotides.

The term "percent identity", as used herein, means the number of identical residues as defined by an optimal alignment using the Smith-Waterman algorithm divided by the length of the overlap multiplied by 100. The alignment is performed by the search program (Pearson, 1991 , Genomics 11 :635-650) with the constraint to align the maximum of both sequences.

The terms "polypeptides" and "proteins" are, where applicable, used interchangeably herein. They may be chemically modified, e.g. post-translationally modified. For example, they may be glycosylated or comprise modified amino acid residues. They may also be modified by the addition of a signal sequence to promote their secretion from a cell where the polypeptide does not naturally contain such a sequence. They may be tagged with a tag. They may be tagged with different labels which may assists in identification of the proteins in a protein complex. Polypeptides/proteins for use in the invention may be in a substantially isolated form. It will be understood that the polypeptid/protein may be mixed with carriers or diluents which will not interfere with the intended purpose of the polypeptide and still be regarded as substantially isolated. A polypeptide/protein for use in the invention may also be in a substantially purified form, in which case it will generally comprise the polypeptide in a preparation in which more than 50%, e.g. more than 80%, 90%, 95% or 99%, by weight of the polypeptide in the preparation is a polypeptide of the invention.

"Target for therapeutic drug" means that the respective protein (target) can bind the active ingredient of a pharmaceutical composition and thereby changes its biological activity in response to the drug binding.

The term "tag" as used herein is meant to be understood in its broadest sense and to include, but is not limited to any suitable enzymatic, fluorescent, or radioactive labels and suitable epitopes, incuding but not limited to HA-tag, Myc-tag, T7, His-tag, FLAG-tag, Calmodulin binding proteins, glutathione-S-transf erase, strep-tag, KT3- epitope, EEF-epitpopes, green-fluorescent protein and variants thereof. The term "therapeutics" as used herein, includes, but is not limited to, a protein complex of the present invention, the individual component proteins, and analogs and derivatives (including fragments); antibodies thereto; nucleic acids encoding the component protein, and analogs or derivatives thereof; component protein antisense nucleic acids, and agents that modulate complex formation and/or activity (i.e., agonists and antagonists).

The term "vector" as used herein means a nucleic acid molecule capable of transporting another nucleic acid sequence to which it has been linked. Preferred vectors are those capable of autonomous replication and/or expression of nueclic acids to which they linked. The terms "plasmid" and "vector" are used interchangeably herein when applicable to the embodiment. However, vectors other than plasmids are also included herein. The expression elements of vectors vary in their strengths and specificities. Depending on the host-vector system utilized, any one of a number of suitable transcription and translation elements may be used.

4. DETAILED DESCRIPTION OF THE INVENTION

Overview:

By applying the process according to the invention said protein complex were identified. The components are listed in table 1.

Said object is further achieved by the characterisation of component proteins. These proteins are listed in table 2.

The invention thus relates to the following embodiments: 1. A protein complex selected from complex (I) and comprising

2. A protein complex comprising a first protein selected from the proteins listed in table 1 , fourth column of a given complex or a homologue or variant thereof, or a functionally active fragment or functionally active derivative of said first protein, the variant being encoded by a nucleic acid that hybridizes to the nucleic acid of said first protein under low stringency conditions, and at least one second protein selected from the group of proteins in table 1, fifth column of a given complex, or a variant or homologue thereof, or a functionally active fragment or a functionally active derivative of said second protein, the variant of said second protein being encoded by a nucleic acid that hybridizes to the nucleic acid of said second protein under low- stringency conditions, and wherein said low stringency conditions comprise hybridization in a buffer comprising 35% formamide, 5X SSC, 50 mM Tris-HCI (pH 7.5), 5 mM EDTA, 0.02% PVP, 0.02% BSA, 100 ug/ml denatured salmon sperm DNA, and 10% (wt/vol) dextran sulfate for 18-20 hours at 40°C, washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4), 5 mM EDTA, and 0.1% SDS for 1-5 hours at 55°C, and washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4) 5 mM EDTA, and 0.1 % SDS for 1.5 hours at 60°C.

3. A protein complex comprising all proteins selected from the proteins in table 1 , third column of a given complex or at least one protein being a homologue thereof, or a variant thereof or functionally active fragment or functionally active derivative of said protein, said variant being encoded by a nucleic acid that hybridizes to the nucleic acid of said protein under low stringency conditions; wherein said low stringency conditions comprise hybridization in a buffer comprising 35% formamide, 5X SSC, 50 mM Tris-HCI (pH 7.5), 5 mM EDTA, 0.02% PVP, 0.02% Ficoll, 0.2% BSA, 100 ug/ml denatured salmon sperm DNA, and 10% (wt/vol) dextran sulfate for 18-20 hours at 40°C, washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4), 5 mM EDTA, and 0.1% SDS for 1-5 hours at 55°C, and washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4), 5 mM EDTA, and 0.1% SDS for 1.5 hours at 60°C.

4. A protein complex that comprises all proteins as listed in table 1 , third column for a given complex or at least one protein being a homologue or a variant thereof, or a functionally active fragment or a functionally active derivative thereof, the variant being encoded by a nucleic acid that hybridizes to the nucleic acid of any of said proteins under low stringency conditions, except at least one protein of the proteins listed in table 5, third column, wherein said low stringency conditions comprise hybridization in a buffer comprising 35% formamide, 5X SSC, 50 mM Tris-HCI (pH 7.5), 5 mM EDTA, 0.02% PVP, 0.02% Ficoll, 0.2% BSA, 100 ug/ml denatured salmon sperm DNA, and 10% (wt/vol) dextran sulfate for 18-20 hours at 40°C, washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4), 5 mM EDTA, and 0.1% SDS for 1-5 hours at 55°C, and washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4), 5 mM EDTA, and 0.1% SDS for 1.5 hours at 60°C, with the provisio that the complex comprises at least one protein selected from table 1 , fifth column of a given complex.

8. The complex of any of No. 1 - 7 that is involved in at least one biochemical activity as stated in table 3.

9. A process for preparing a complex of any of No. 1 - 8 and optionally the components thereof comprising the following steps: expressing a protein of the complex, preferably a tagged protein, in a target cell, or a tissue or an organ, isolating the protein complex which is attached to the protein, preferably the tagged protein, and optionally disassociating the protein complex and isolating the individual complex members.

13. Protein selected from the group of proteins in table 1 , sixth column of a given complex or a homologue or a variant of thereof, or a functionally active fragment or a functionally active derivative of said protein, the variant being encoded by a nucleic acid that hybridizes to the nucleic acid encoding said protein under low stringency conditions, wherein said low stringency conditions comprise hybridization in a buffer comprising 35% formamide, 5X SSC, 50 mM Tris-HCI (pH 7.5), 5 mM EDTA, 0.02% PVP, 0.02% Ficoll, 0.2% BSA, 100 ug/ml denatured salmon sperm DNA, and 10% (wt/vol) dextran sulfate for 18-20 hours at 40°C, washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4), 5 mM EDTA, and 0.1% SDS for 1.5 hours at 55°C, and washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4), 5 mM EDTA, and 0.1 % SDS for 1.5 hours at 60°C.

14. Nucleic acid encoding a protein according to No. 13.

15. Construct, preferably a vector construct, comprising

(a) a nucleic acid according to No. 14 and at least one further nucleic acid which is normally not associated with said nucleic acid, or

(b) at least two separate nucleic acid sequences each encoding a different protein, or a functionally active fragment or a functionally active derivative thereof, or a homologue or a variant thereof, at least one of said proteins being selected from the first group of proteins according to No. 1 (a) and at least one of said proteins, being selected from the second group of proteins according to No. 1 (b) or

17. An antibody or a fragment of said antibody containing the binding domain thereof, selected from an antibody or fragment thereof, which binds the complex of any of No. 1 - 8 and which does not bind any of the proteins of said complex when uncomplexed and an antibody or a fragment of said antibody containing the binding domain thereof which binds to any of the proteins of the group of proteins according to No. 13. 18. A kit comprising in one or more containers:

(a) the complex of any of No. 1 - 8 and/or the proteins of No. 13 and/or

(b) an antibody according to No. 17 and/or

(e) further components such as reagents, buffers and working instructions.

19. The kit according to No. 18 for processing a substrate of a complex of any one of No. 1 - 8.

20. The kit according to No. 18 for the diagnosis or prognosis of a disease or a disease risk, preferentially for a disease or disorder such as those as stated in column 2, table 4 of a given complex.

25. A method for screening for a molecule that binds to a complex of any one of No. 1 - 8 and/or a protein of No. 13, comprising the following steps: (a) exposing said complex or protein, or a cell or organism containing said complex or said protein, to one or more candidate molecules; and

27. The method of No. 26, wherein the amount of said complex is determined.

28. The method of No. 26, wherein the activity of said complex is determined.

29. The method of No. 28, wherein said determining step comprises isolating from the cell or organism said complex to produce said isolated complex and contacting said isolated complex in the presence or absence of a candidate molecule with a substrate of said complex and determining whether said substrate is processed in the absence of the candidate molecule and whether the processing of said substrate is modified in the presence of said candidate molecule. 30. The method of No. 26, wherein the amount of the individual protein components of said complex is determined.

32. The method of any of No. 26 - 31 , wherein said method is a method of screening for a drug for treatment or prevention of a disease or disorder, preferentially of a disease or disorder selected from the diseases or disorders such as those as stated in column 2, table 4 of a given complex.

33. Use of a molecule that modulates the amount of, activity of, or the protein components of the complex of any one of No. 1 - 8 for the manufacture of a medicament for the treatment or prevention of a disease or disorder, preferentially of a disease or disorder such as those as stated in column 2, table 4 of a given complex.

36. The method of No. 35, wherein the amount of said complex is determined.

37. The method of No. 35, wherein the activity of said complex is determined.

42. A method for treating or preventing a disease or disorder characterized by an aberrant amount of, activity of, component composition of or intracellular localization of, the complex of any one of No. 1 - 8, comprising administering to a subject in need of such treatment or prevention a therapeutically effective amount of one or more molecules that modulate the amount of, activity of, or protein composition of, said complex. 43. The method according to No. 42, wherein said disease or disorder involves decreased levels of the amount or activity of said complex.

Animal models are also provided herein.

Preferably, the protein components of the complexes described herein are all mammalian proteins. The complexes can also consist only of the respective homologues from other mammals such as mouse, rat, pig, cow, dog, monkey, sheep or horse or other species such as D. melanogaster, C. elegans or chicken. In another preferred embodiment, the complexes are a mixture of proteins from two or more species.

TABLES:

Table 1 : Composition of Complexes

First column (^'Name of complex^'): Lists the name of the protein complexes as used herein.

Second column ('Entry point'): Lists the bait proteins that have been chosen for the purification of the given complex.

Third column (^'All interactors'): Lists all novel interactors which have been identified as members of the complex and all interactors which have been known to be associated with the bait so far.

Fourth column (^'Known interactors^'): Lists all interactors which have been known to be associated with the bait so far.

Fifth column (^'Novel interactors of the complex^'): Lists all novel interactors of the complex which have been identified in the experiments provided herein. Sixth column: Separately lists the members of the newly identified complex which have not been annotated previously.

Table 2: Individual Proteins of the Complexes

First column (^'Protein^'): Lists in alphabetical order all proteins which have been identified as interactors of the complexes presented herein.

Second column (^'SEQ ID^'): Lists the SEQ ID (Sequence Identifications) of the proteins herein as used herein.

Third column C IPI-Numbers^'): Lists the IPI-Numbers of the proteins herein. The IPI-

Numbers refer to the International Protein Index created by the European Bioinformatics

Institute (EMBL-EBI), Hinxton, UK.

Fourth column f Molecular Weighf ): Lists the Molecular Weight of the proteins in Dalton.

Table 3: Biochemical Activities of the Complexes of the invention.

Second column (^'Biochemical Activity^'): Lists biochemical activities of the complexes.

Assays in order to test these activities are also provided herein (infra).

Table 4: Medical Applications of the Complexes of the invention

First column (^'Name of complex^'): Lists the name of the protein compelxes as used herein

Second column (^'Medical application^'): lists disorder, diseases, disease areas etc. which are treatable and/or preventable and/or diagnosable etc. by therapeutics and methods interacting with/acting via the complex.

4.1 PROTEIN COMPLEXES/PROTEINS OF THE INVENTION

The protein complexes of the present invention and their component proteins are described in the Tables 1 - 4. The protein complexes and component proteins can be obtained by methods well known in the art for protein purification and recombinant protein expression. For example, the protein complexes of the present invention can be isolated using the TAP method described in Section 5, infra, and in WO 00/09716 and Rigaut et al., 1999, Nature Biotechnol. 17:1030-1032, which are each incorporated by reference in their entirety. Additionally, the protein complexes can be isolated by immunoprecipitation of the component proteins and combining the immunoprecipitated proteins. The protein complexes can also be produced by recombinantly expressing the component proteins and combining the expressed proteins.

The nucleic and amino acid sequences of the component proteins of the protein complexes of the present invention are provided herein (SEQ ID NO 1 - 198), and can be obtained by any method known in the art, e.g., by PCR amplification using synthetic primers hybridizable to the 3' and 5' ends of each sequence, and/or by cloning from a cDNA or genomic library using an oligonucleotide specific for each nucleotide sequence.

Homologues (e.g., nucleic acids encoding component proteins from other species) or other related sequences (e.g., variants, paralogs) which are members of a native cellular protein complex can be obtained by low, moderate or high stringency hybridization with all or a portion of the particular nucleic acid sequence as a probe,^" using methods well known in the art for nucleic acid hybridization and cloning.

Exemplary moderately stringent hybridization conditions are as follows: prehybridization of filters containing DNA is carried out for 8 hours to overnight at 65°C in buffer composed of 6X SSC, 50 mM Tris-HCI (pH 7.5), 1 mM EDTA, 0.02% PVP, 0.02% Ficoll, 0.02% BSA, and 500 μg/ml denatured salmon sperm DNA. Filters are hybridized for 48 hours at 65°C in prehybridization mixture containing 100 μg/ml denatured salmon sperm DNA and 5-20 X 10⁶ cpm of ³²P-labeled probe. Washing of filters is done at 37°C for 1 hour in a solution containing 2X SSC, 0.01% PVP, 0.01% Ficoll, and 0.01% BSA. This is followed by a wash in 0.1X SSC at 50 °C for 45 min before autoradiography. Alternatively, exemplary conditions of high stringency are as follows: e.g., hybridization to filter-bound DNA in 0.5 M NaHPO₄, 7% sodium dodecyl sulfate (SDS), 1 mM EDTA at 65°C, and washing in 0.1xSSC/0.1% SDS at 68°C (Ausubel et al., eds., 1989, Current Protocols in Molecular Biology, Vol. I, Green Publishing Associates, Inc., and John Wiley & sons, Inc., New York, at p. 2.10.3). Other conditions of high stringency which may be used are well known in the art. Exemplary low stringency hybridization conditions comprise hybridization in a buffer comprising 35% formamide, 5X SSC, 50 mM Tris-HCI (pH 7.5), 5 mM EDTA, 0.02% PVP, 0.02% Ficoll, 0.2% BSA, 100 μg/ml denatured salmon sperm DNA, and 10% (wt/vol) dextran sulfate for 18-20 hours at 40°C, washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4), 5 mM EDTA, and 0.1 % SDS for 1.5 hours at 55°C, and washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4), 5 mM EDTA, and 0.1% SDS for 1.5 hours at 60°C. For recombinant expression of one or more of the proteins, the nucleic acid containing all or a portion of the nucleotide sequence encoding the protein can be inserted into an appropriate expression vector, i.e., a vector that contains the necessary elements for the transcription and translation of the inserted protein coding sequence. The necessary transcriptional and translational signals can also be supplied by the native promoter of the component protein gene, and/or flanking regions.

A variety of host-vector systems may be utilized to express the protein coding sequence. These include but are not limited to mammalian cell systems infected with virus (e.g., vaccinia virus, adenovirus, etc.); insect cell systems infected with virus (e.g., baculovirus); microorganisms such as yeast containing yeast vectors; or bacteria transformed with bacteriophage, DNA, plasmid DNA, or cosmid DNA. The expression elements of vectors vary in their strengths and specificities. Depending on the host- vector system utilized, any one of a number of suitable transcription and translation elements may be used.

In a preferred embodiment, a complex of the present invention is obtained by expressing the entire coding sequences of the component proteins in the same cell, either under the control of the same promoter or separate promoters. In yet another embodiment, a derivative, fragment or homologue of a component protein is recombinantly expressed. Preferably the derivative, fragment or homologue of the protein forms a complex with the other components of the complex, and more preferably forms a complex that binds to an anti-complex antibody. Such an antibody is further described infra.

Any method available in the art can be used for the insertion of DNA fragments into a vector to construct expression vectors containing a chimeric gene consisting of appropriate transcriptional/translational control signals and protein coding sequences. These methods may include in vitro recombinant DNA and synthetic techniques and in vivo recombinant techniques (genetic recombination). Expression of nucleic acid sequences encoding a component protein, or a derivative, fragment or homologue thereof, may be regulated by a second nucleic acid sequence so that the gene or fragment thereof is expressed in a host transformed with the recombinant DNA molecule(s). For example, expression of the proteins may be controlled by any promoter/enhancer known in the art. In a specific embodiment, the promoter is not native to the gene for the component protein. Promoters that may be used can be selected from among the many known in the art, and are chosen so as to be operative in the selected host cell.

In a specific embodiment, a vector is used that comprises a promoter operably linked to nucleic acid sequences encoding a component protein, or a fragment, derivative or homologue thereof, one or more origins of replication, and optionally, one or more selectable markers (e.g., an antibiotic resistance gene).

In another specific embodiment, an expression vector containing the coding sequence, or a portion thereof, of a component protein, either together or separately, is made by subcloning the gene sequences into the EcoRI restriction site of each of the three pGEX vectors (glutathione S-transferase expression vectors; Smith and Johnson, 1988, Gene 7:31-40). This allows for the expression of products in the correct reading frame.

Expression vectors containing the sequences of interest can be identified by three general approaches: (a) nucleic acid hybridization, (b) presence or absence of "marker" gene function, and (c) expression of the inserted sequences. In the first approach, coding sequences can be detected by nucleic acid hybridization to probes comprising sequences homologous and complementary to the inserted sequences. In the second approach, the recombinant vector/host system can be identified and selected based upon the presence or absence of certain "marker" functions (e.g., resistance to antibiotics, occlusion body formation in baculovirus, etc.) caused by insertion of the sequences of interest in the vector. For example, if a component protein gene, or portion thereof, is inserted within the marker gene sequence of the vector, recombinants containing the encoded protein or portion will be identified by the absence of the marker gene function (e.g., loss of β-galactosidase activity). In the third approach, recombinant expression vectors can be identified by assaying for the component protein expressed by the recombinant vector. Such assays can be based, for example, on the physical or functional properties of the interacting species in in vitro assay systems, e.g., formation of a complex comprising the protein or binding to an anti-complex antibody.

Once recombinant component protein molecules are identified and the complexes or individual proteins isolated, several methods known in the art can be used to propagate them. Using a suitable host system and growth conditions, recombinant expression vectors can be propagated and amplified in quantity. As previously described, the expression vectors or derivatives which can be used include, but are not limited to, human or animal viruses such as vaccinia virus or adenovirus; insect viruses such as baculovirus, yeast vectors; bacteriophage vectors such as lambda phage; and plasmid and cosmid vectors.

In addition, a host cell strain may be chosen that modulates the expression of the inserted sequences, or modifies or processes the expressed proteins in the specific fashion desired. Expression from certain promoters can be elevated in the presence of certain inducers; thus expression of the genetically-engineered component proteins may be controlled. Furthermore, different host cells have characteristic and specific mechanisms for the translational and post-translational processing and modification (e.g., glycosylation, phosphorylation, etc.) of proteins. Appropriate cell lines or host systems can be chosen to ensure that the desired modification and processing of the foreign protein is achieved. For example, expression in a bacterial system can be used to produce an unglycosylated core protein, while expression in mammalian cells ensures "native" glycosylation of a heterologous protein. Furthermore, different vector/host expression systems may effect processing reactions to different extents.

In other specific embodiments, a component protein or a fragment, homologue or derivative thereof, may be expressed as fusion or chimeric protein product comprising the protein, fragment, homologue, or derivative joined via a peptide bond to a heterologous protein sequence of a different protein. Such chimeric products can be made by ligating the appropriate nucleic acid sequences encoding the desired amino acids to each other by methods known in the art, in the proper coding frame, and expressing the chimeric products in a suitable host by methods commonly known in the art. Alternatively, such a chimeric product can be made by protein synthetic techniques, e.g., by use of a peptide synthesizer. Chimeric genes comprising a portion of a component protein fused to any heterologous protein-encoding sequences may be constructed.

In particular, protein component derivatives can be made by altering their sequences by substitutions, additions or deletions that provide for functionally equivalent molecules. Due to the degeneracy of nucleotide coding sequences, other DNA sequences that encode substantially the same amino acid sequence as a component gene or cDNA can be used in the practice of the present invention. These include but are not limited to nucleotide sequences comprising all or portions of the component protein gene that are altered by the substitution of different codons that encode a functionally equivalent amino acid residue within the sequence, thus producing a silent change. Likewise, the derivatives of the invention include, but are not limited to, those containing, as a primary amino acid sequence, all or part of the amino acid sequence of a component protein, including altered sequences in which functionally equivalent amino acid residues are substituted for residues within the sequence resulting in a silent change. For example, one or more amino acid residues within the sequence can be substituted by another amino acid of a similar polarity that acts as a functional equivalent, resulting in a silent alteration. Substitutes for an amino acid within the sequence may be selected from other members of the class to which the amino acid belongs. For example, the nonpolar (hydrophobic) amino acids include alanine, leucine, isoleucine, valine, proline, phenylalanine, tryptophan and methionine. The polar neutral amino acids include glycine, serine, threonine, cysteine, tyrosine, asparagine, and glutamine. The positively charged (basic) amino acids include arginine, lysine and histidine. The negatively charged (acidic) amino acids include aspartic acid and glutamic acid.

In a specific embodiment, up to 1%, 2%, 5%, 10%, 15% or 20% of the total number of amino acids in the wild type protein are substituted or deleted; or 1 , 2, 3, 4, 5, or 6 or up to 10 or up to 20 amino acids are inserted, substituted or deleted relative to the wild type protein.

In a specific embodiment of the invention, the nucleic acids encoding a protein component and protein components consisting of or comprising a fragment of or consisting of at least 6 (continuous) amino acids of the protein are provided. In other embodiments, the fragment consists of at least 10, 20, 30, 40, or 50 amino acids of the component protein. In specific embodiments, such fragments are not larger than 35, 100 or 200 amino acids. Derivatives or analogs of component proteins include, but are not limited, to molecules comprising regions that are substantially homologous to the component proteins, in various embodiments, by at least 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95% or 99% identity over an amino acid sequence of identical size or when compared to an aligned sequence in which the alignment is done by a computer homology program known in the art, or whose encoding nucleic acid is capable of hybridizing to a sequence encoding the component protein under stringent, moderately stringent, or nonstringent conditions.

In a specific embodiment, proteins are provided herein, which share an identical region of 20, 30, 40, 50 or 60 contiguous amino acids of the proteins listed in table 2.

The protein component derivatives and analogs of the invention can be produced by various methods known in the art. The manipulations which result in their production can occur at the gene or protein level. For example, the cloned gene sequences can be modified by any of numerous strategies known in the art (Sambrook et al., 1989, Molecular Cloning, A Laboratory Manual, 2d Ed., Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York). The sequences can be cleaved at appropriate sites with restriction endonuclease(s), followed by further enzymatic modification if desired, isolated, and ligated in vitro. In the production of the gene encoding a derivative, homologue or analog of a component protein, care should be taken to ensure that the modified gene retains the original translational reading frame, uninterrupted by translational stop signals, in the gene region where the desired activity is encoded.

Additionally, the encoding nucleic acid sequence can be mutated in vitro or in vivo, to create and/or destroy translation, initiation, and/or termination sequences, or to create variations in coding regions and/or form new restriction endonuclease sites or destroy pre-existing ones, to facilitate further in vitro modification. Any technique for mutagenesis known in the art can be used, including but not limited to, chemical mutagenesis and in vitro site-directed mutagenesis (Hutchinson et al., 1978, J. Biol. Chem. 253:6551-6558), amplification with PCR primers containing a mutation, etc.

Once a recombinant cell expressing a component protein, or fragment or derivative thereof, is identified, the individual gene product or complex can be isolated and analyzed. This is achieved by assays based on the physical and/or functional properties of the protein or complex, including, but not limited to, radioactive labeling of the product followed by analysis by gel electrophoresis, immunoassay, cross-linking to marker-labeled product, etc.

The component proteins and complexes may be isolated and purified by standard methods known in the art (either from natural sources or recombinant host cells expressing the complexes or proteins), including but not restricted to column chromatography (e.g., ion exchange, affinity, gel exclusion, reversed-phase high pressure, fast protein liquid, etc.), differential centrifugation, differential solubility, or by any other standard technique used for the purification of proteins. Functional properties may be evaluated using any suitable assay known in the art.

Alternatively, once a component protein or its derivative, is identified, the amino acid sequence of the protein can be deduced from the nucleic acid sequence of the chimeric gene from which it was encoded. As a result, the protein or its derivative can be synthesized by standard chemical methods known in the art (e.g., Hunkapiller et al., 1984, Nature 310:105-111). Manipulations of component protein sequences may be made at the protein level. Included within the scope of the invention is a complex in which the component proteins or derivatives and analogs that are differentially modified during or after translation, e.g., by glycosylation, acetylation, phosphorylation, amidation, derivatization by known protecting/blocking groups, proteolytic cleavage, linkage to an antibody molecule or other cellular ligand, etc. Any of numerous chemical modifications may be carried out by known techniques, including but not limited to specific chemical cleavage by cyanogen bromide, trypsin, chymotrypsin, papain, V8 protease, NaBH₄, acetylation, formylation, oxidation, reduction, metabolic synthesis in the presence of tunicamycin, etc.

In specific embodiments, the amino acid sequences are modified to include a fluorescent label. In another specific embodiment, the protein sequences are modified to have a heterofunctional reagent; such heterofunctional reagents can be used to crosslink the members of the complex.

In addition, complexes of analogs and derivatives of component proteins can be chemically synthesized. For example, a peptide corresponding to a portion of a component protein, which comprises the desired domain or mediates the desired activity in vitro (e.g., complex formation) can be synthesized by use of a peptide synthesizer. Furthermore, if desired, non-classical amino acids or chemical amino acid analogs can be introduced as a substitution or addition into the protein sequence.

In cases where natural products are suspected of being mutant or are isolated from new species, the amino acid sequence of a component protein isolated from the natural source, as well as those expressed in vitro, or from synthesized expression vectors in vivo or in vitro, can be determined from analysis of the DNA sequence, or alternatively, by direct sequencing of the isolated protein. Such analysis can be performed by manual sequencing or through use of an automated amino acid sequenator.

The complexes can also be analyzed by hydrophilicity analysis (Hopp and Woods, 1981 , Proc. Natl. Acad. Sci. USA 78:3824-3828). A hydrophilicity profile can be used to identify the hydrophobic and hydrophilic regions of the proteins, and help predict their orientation in designing substrates for experimental manipulation, such as in binding experiments, antibody synthesis, etc. Secondary structural analysis can also be done to identify regions of the component proteins, or their derivatives, that assume specific structures (Chou and Fasman, 1974, Biochemistry 13:222-23). Manipulation, translation, secondary structure prediction, hydrophilicity and hydrophobicity profile predictions, open reading frame prediction and plotting, and determination of sequence homologies, etc., can be accomplished using computer software programs available in the art.

Other methods of structural analysis including but not limited to X-ray crystallography (Engstrom, 1974, Biochem. Exp. Biol. 11 :7-13), mass spectroscopy and gas chromatography (Methods in Protein Science, J. Wiley and Sons, New York, 1997), and computer modeling (Fletterick and Zoller, eds., 1986, Computer Graphics and Molecular Modeling, In: Current Communications in Molecular Biology, Cold Spring Harbor Laboratory, Cold Spring Harbor Press, New York) can also be employed.

4.2 ANTIBODIES TO PROTEIN COMPLEXES/PROTEINS OF THE INVENTION

According to the present invention, a protein complex of the present invention comprising a first protein, or a functionally active fragment or functionally active derivative thereof, selected from the group consisting of proteins listed in fourth column of table 1 ; and a second protein, or a functionally active fragment or functionally active derivative thereof, selected from the group consisting of proteins listed in fifth column of table 1 , or a functionally active fragment or functionally active derivative thereof, can be used as an immunogen to generate antibodies which immunospecificaily bind such immunogen. According to the present invention, also a protein complex of the present invention can be used as an immunogen to generate antibodies which immunospecificaily bind to such immunogen comprising all proteins listed in fifth column of table 1.

Such antibodies include, but are not limited to, polyclonal, monoclonal, chimeric, single chain, Fab fragments, and an Fab expression library. In a specific embodiment, antibodies to a complex comprising human protein components are produced. In another embodiment, a complex formed from a fragment of said first protein and a fragment of said second protein, which fragments contain the protein domain that interacts with the other member of the complex, are used as an immunogen for antibody production. In a preferred embodiment, the antibody specific for the complex in that the antibody does not bind the individual protein components of the complex.

Polyclonal antibodies can be prepared as described above by immunizing a suitable subject with a polypeptide of the invention as an immunogen. Preferred polyclonal antibody compositions are ones that have been selected for antibodies directed against a polypeptide or polypeptides of the invention. Particularly preferred polyclonal antibody preparations are ones that contain only antibodies directed against a polypeptide or polypeptides of the invention. Particularly preferred immunogen compositions are those that contain no other human proteins such as, for example, immunogen compositions made using a non-human host cell for recombinant expression of a polypeptide of the invention. In such a manner, the only human epitope or epitopes recognized by the resulting antibody compositions raised against this immunogen will be present as part of a polypeptide or polypeptides of the invention.

The antibody titer in the immunized subject can be monitored over time by standard techniques, such as with an enzyme linked immunosorbent assay (ELISA) using immobilized polypeptide. If desired, the antibody molecules can be isolated from the mammal (e.g., from the blood) and further purified by well-known techniques, such as protein A chromatography to obtain the IgG fraction. Alternatively, antibodies specific for a protein or polypeptide of the invention can be selected for (e.g., partially purified) or purified by, e.g., affinity chromatography. For example, a recombinantly expressed and purified (or partially purified) protein of the invention is produced as described herein, and covalently or non-covalently coupled to a solid support such as, for example, a chromatography column. The column can then be used to affinity purify antibodies specific for the proteins of the invention from a sample containing antibodies directed against a large number of different epitopes, thereby generating a substantially purified antibody composition, i.e., one that is substantially free of contaminating antibodies. By a substantially purified antibody composition is meant, in this context, that the antibody sample contains at most only 30% (by dry weight) of contaminating antibodies directed against epitopes other than those on the desired protein or polypeptide of the invention, and preferably at most 20%, yet more preferably at most 10%, and most preferably at most 5% (by dry weight) of the sample is contaminating antibodies. A purified antibody composition means that at least 99% of the antibodies in the composition are directed against the desired protein or polypeptide of the invention.

At an appropriate time after immunization, e.g., when the specific antibody titers are highest, antibody-producing cells can be obtained from the subject and used to prepare monoclonal antibodies by standard techniques, such as the hybridoma technique originally described by Kohler and Milstein, 1975, Nature 256:495-497, the human B cell hybridoma technique (Kozbor et al., 1983, Immunol. Today 4:72), the EBV-hybridoma technique (Cole et al., 1985, Monoclonal Antibodies and Cancer Therapy, Alan R. Liss, Inc., pp. 77-96) or trioma techniques. The technology for producing hybridomas is well known (see generally Current Protocols in Immunology 1994, Coligan et al. (eds.) John Wiley & Sons, Inc., New York, NY). Hybridoma cells producing a monoclonal antibody of the invention are detected by screening the hybridoma culture supernatants for antibodies that bind the polypeptide of interest, e.g., using a standard ELISA assay.

Alternative to preparing monoclonal antibody-secreting hybridomas, a monoclonal antibody directed against a polypeptide of the invention can be identified and isolated by screening a recombinant combinatorial immunoglobulin library (e.g., an antibody phage display library) with the polypeptide of interest. Kits for generating and screening phage display libraries are commercially available (e.g., the Pharmacia Recombinant Phage Antibody System, Catalog No. 27-9400-01 ; and the Stratagene SurfZAP Phage Display Kit, Catalog No. 240612). Additionally, examples of methods and reagents particularly amenable for use in generating and screening antibody display library can be found in, for example, U.S. Patent No. 5,223,409; PCT Publication No. WO 92/18619; PCT Publication No. WO 91/17271 ; PCT Publication No. WO 92/20791 ; PCT Publication No. WO 92/15679; PCT Publication No. WO 93/01288; PCT Publication No. WO 92/01047; PCT Publication No. WO 92/09690; PCT Publication No. WO 90/02809; Fuchs et al., 1991 , Bio/Technology 9:1370-1372; Hay et al., 1992, Hum. Antibod. Hybridomas 3:81-85; Huse et al., 1989, Science 246:1275-1281 ; Griffiths et al., 1993, EMBO J. 12:725-734.

Additionally, recombinant antibodies, such as chimeric and humanized monoclonal antibodies, comprising both human and non-human portions, which can be made using standard recombinant DNA techniques, are within the scope of the invention. A chimeric antibody is a molecule in which different portions are derived from different animal species, such as those having a variable region derived from a murine mAb and a human immunoglobulin constant region. (See, e.g., Cabilly et al., U.S. Patent No. 4,816,567; and Boss et al., U.S. Patent No. 4,816,397, which are incorporated herein by reference in their entirety.) Humanized antibodies are antibody molecules from non- human species having one or more complementarily determining regions (CDRs) from the non-human species and a framework region from a human immunoglobulin molecule. (See, e.g., Queen, U.S. Patent No. 5,585,089, which is incorporated herein by reference in its entirety.) Such chimeric and humanized monoclonal antibodies can be produced by recombinant DNA techniques known in the art, for example using methods described in PCT Publication No. WO 87/02671 ; European Patent Application 184,187; European Patent Application 171 ,496; European Patent Application 173,494; PCT Publication No. WO 86/01533; U.S. Patent No. 4,816,567; European Patent Application 125,023; Better et al., 1988, Science 240:1041-1043; Liu et al., 1987, Proc. Natl. Acad. Sci. USA 84:3439-3443; Liu et al., 1987, J. Immunol. 139:3521-3526; Sun et al., 1987, Proc. Natl. Acad. Sci. USA 84:214-218; Nishimura et al., 1987, Cane. Res. 47:999-1005; Wood et al., 1985, Nature 314:446-449; and Shaw et al., 1988, J. Natl. Cancer Inst. 80:1553-1559); Morrison, 1985, Science 229:1202-1207; Oi et al., 1986, Bio/Techniques 4:214; U.S. Patent 5,225,539; Jones et al., 1986, Nature 321 :552-525; Verhoeyan et al., 1988, Science 239:1534; and Beidler et al., 1988, J. Immunol. 141 :4053-4060.

Completely human antibodies are particularly desirable for therapeutic treatment of human patients. Such antibodies can be produced, for example, using transgenic mice which are incapable of expressing endogenous immunoglobulin heavy and light chains genes, but which can express human heavy and light chain genes. The transgenic mice are immunized in the normal fashion with a selected antigen, e.g., all or a portion of a polypeptide of the invention. Monoclonal antibodies directed against the antigen can be obtained using conventional hybridoma technology. The human immunoglobulin transgenes harbored by the transgenic mice rearrange during B cell differentiation, and subsequently undergo class switching and somatic mutation. Thus, using such a technique, it is possible to produce therapeutically useful IgG, IgA and IgE antibodies. For an overview of this technology for producing human antibodies, see Lonberg and Huszar, 1995, Int. Rev. Immunol. 13:65-93). For a detailed discussion of this technology for producing human antibodies and human monoclonal antibodies and protocols for producing such antibodies, see, e.g., U.S. Patent 5,625,126; U.S. Patent 5,633,425; U.S. Patent 5,569,825; U.S. Patent 5,661 ,016; and U.S. Patent 5,545,806. In addition, companies such as Abgenix, Inc. (Freemont, CA), can be engaged to provide human antibodies directed against a selected antigen using technology similar to that described above.

Completely human antibodies which recognize a selected epitope can be generated using a technique referred to as "guided selection." In this approach a selected non-human monoclonal antibody, e.g., a murine antibody, is used to guide the selection of a completely human antibody recognizing the same epitope. (Jespers et al., 1994, Bio/technology 12:899-903). Antibody fragments that contain the idiotypes of the complex can be generated by techniques known in the art. For example, such fragments include, but are not limited to, the F(ab')2 fragment which can be produced by pepsin digestion of the antibody molecule; the Fab' fragment that can be generated by reducing the disulfide bridges of the F(ab')2 fragment; the Fab fragment that can be generated by treating the antibody molecular with papain and a reducing agent; and Fv fragments.

In the production of antibodies, screening for the desired antibody can be accomplished by techniques known in the art, e.g., ELISA (enzyme-linked immunosorbent assay). To select antibodies specific to a particular domain of the complex, or a derivative thereof, one may assay generated hybridomas for a product that binds to the fragment of the complex, or a derivative thereof, that contains such a domain. For selection of an antibody that specifically binds a complex of the present, or a derivative, or homologue thereof, but which does not specifically bind to the individual proteins of the complex, or a derivative, or homologue thereof, one can select on the basis of positive binding to the complex and a lack of binding to the individual protein components.

Antibodies specific to a domain of the complex, or a derivative, or homologue thereof, are also provided.

The foregoing antibodies can be used in methods known in the art relating to the localization and/or quantification of the complexes of the invention, e.g., for imaging these proteins, measuring levels thereof in appropriate physiological samples (by immunoassay), in diagnostic methods, etc. This hold true also for a derivative, or homologue thereof of a complex.

In another embodiment of the invention (see infra), an antibody to a complex or a fragment of such antibodies containing the antibody binding domain, is a therapeutic.

4.3 DIAGNOSTIC. PROGNOSTIC. AND SCREENING USES OF THE PROTEIN COMPLEXES/PROTEINS OF THE INVENTION

The particular protein complexes and proteins of the present invention may be markers of normal physiological processes, and thus have diagnostic utility. Further, definition of particular groups of patients with elevations or deficiencies of a protein complex of the present invention, or wherein the protein complex has a change in protein component composition, can lead to new nosological classifications of diseases, furthering diagnostic ability.

Examples for diseases or disorders are those as listed in table 4

Detecting levels of protein complexes, or individual component proteins that form the complexes, or detecting levels of the mRNAs encoding the components of the complex, may be used in diagnosis, prognosis, and/or staging to follow the course of a disease state, to follow a therapeutic response, etc.

A protein complex of the present invention and the individual components of the complex and a derivative, analog or subsequence thereof, encoding nucleic acids (and sequences complementary thereto), and anti-complex antibodies and antibodies directed against individual components that can form the complex, are useful in diagnostics. The foregoing molecules can be used in assays, such as immunoassays, to detect, prognose, diagnose, or monitor various conditions, diseases, and disorders characterized by aberrant levels of a complex or aberrant component composition of a complex, or monitor the treatment of such various conditions, diseases, and disorders.

In particular, such an immunoassay is carried out by a method comprising contacting a sample derived from a patient with an anti-complex antibody under conditions such that immunospecific binding can occur, and detecting or measuring the amount of any immunospecific binding by the antibody. In a specific aspect, such binding of antibody, in tissue sections, can be used to detect aberrant complex localization, or aberrant (e.g., high, low or absent) levels of a protein complex or complexes. In a specific embodiment, an antibody to the complex can be used to assay a patient tissue or serum sample for the presence of the complex, where an aberrant level of the complex is an indication of a diseased condition. By "aberrant levels" is meant increased or decreased levels relative to that present, or a standard level representing that present, in an analogous sample from a portion or fluid of the body, or from a subject not having the disorder.

The immunoassays which can be used include but are not limited to competitive and non-competitive assay systems using techniques such as Western blots, radioimmunoassays, ELISA (enzyme linked immunosorbent assay), "sandwich" immunoassays, immunoprecipitation assays, precipitin reactions, gel diffusion precipitin reactions, immunodiffusion assays, agglutination assays, complement-fixation assays, immunoradiometric assays, fluorescent immunoassays, protein A immunoassays, to name but a few known in the art. Nucleic acids encoding the components of the protein complex and related nucleic acid sequences and subsequences, including complementary sequences, can be used in hybridization assays. The nucleic acid sequences, or subsequences thereof, comprising about at least 8 nucleotides, can be used as hybridization probes. Hybridization assays can be used to detect, prognose, diagnose, or monitor conditions, disorders, or disease states associated with aberrant levels of the mRNAs encoding the components of a complex as described, supra. In particular, such a hybridization assay is carried out by a method comprising contacting a sample containing nucleic acid with a nucleic acid probe capable of hybridizing to component protein coding DNA or RNA, under conditions such that hybridization can occur, and detecting or measuring any resulting hybridization.

In specific embodiments, diseases and disorders involving or characterized by aberrant levels of a protein complex or aberrant complex composition can be diagnosed, or its suspected presence can be screened for, or a predisposition to develop such disorders can be detected, by determining the component protein composition of the complex, or detecting aberrant levels of a member of the complex or un-complexed component proteins or encoding nucleic acids, or functional activity including, but not restricted to, binding to an interacting partner, or by detecting mutations in component protein RNA, DNA or protein (e.g., mutations such as translocations, truncations, changes in nucleotide or amino acid sequence relative to wild-type that cause increased or decreased expression or activity of a complex, and/or component protein.

Such diseases and disorders include, but are not limited to neurodegenerative disease such as listed in table 4.

By way of example, levels of a protein complex and the individual components of a complex can be detected by immunoassay, levels of component protein RNA or DNA can be detected by hybridization assays (e.g., Northern blots, dot blots, RNase protection assays), and binding of component proteins to each other (e.g., complex formation) can be measured by binding assays commonly known in the art. Translocations and point mutations in component protein genes can be detected by Southern blotting, RFLP analysis, PCR using primers that preferably generate a fragment spanning at least most of the gene by sequencing of genomic DNA or cDNA obtained from the patient, etc.

Assays well known in the art (e.g., assays described above such as immunoassays, nucleic acid hybridization assays, activity assays, etc.) can be used to determine whether one or more particular protein complexes are present at either increased or decreased levels, or are absent, in samples from patients suffering from a particular disease or disorder, or having a predisposition to develop such a disease or disorder, as compared to the levels in samples from subjects not having such a disease or disorder, or having a predisposition to develop such a disease or disorder. Additionally, these assays can be used to determine whether the ratio of the complex to the un-complexed components of the complex, is increased or decreased in samples from patients suffering from a particular disease or disorder, or having a predisposition to develop such a disease or disorder, as compared to the ratio in samples from subjects not having such a disease or disorder.

In the event that levels of one or more particular protein complexes (i.e., complexes formed from component protein derivatives, homologs, fragments, or analogs) are determined to be increased in patients suffering from a particular disease or disorder, or having a predisposition to develop such a disease or disorder, then the particular disease or disorder, or predisposition for a disease or disorder, can be diagnosed, have prognosis defined for, be screened for, or be monitored by detecting increased levels of the one or more protein complexes, increased levels of the mRNA that encodes one or more members of the one or more particular protein complexes, or by detecting increased complex functional activity.

Accordingly, in a specific embodiment of the present invention, diseases and disorders involving increased levels of one or more protein complexes can be diagnosed, or their suspected presence can be screened for, or a predisposition to develop such disorders can be detected, by detecting increased levels of the one or more protein complexes, the mRNA encoding both members of the complex, or complex functional activity, or by detecting mutations in the component proteins that stabilize or enhance complex formation, e.g., mutations such as translocations in nucleic acids, truncations in the gene or protein, changes in nucleotide or amino acid sequence relative to wild-type, that stabilize or enhance complex formation.

In the event that levels of one or more particular protein complexes are determined to be decreased in patients suffering from a particular disease or disorder, or having a predisposition to develop such a disease or disorder, then the particular disease or disorder or predisposition for a disease or disorder can be diagnosed, have its prognosis determined, be screened for, or be monitored by detecting decreased levels of the one or more protein complexes, the mRNA that encodes one or more members of the particular one or more protein complexes, or by detecting decreased protein complex functional activity.

Accordingly, in a specific embodiment of the invention, diseases and disorders involving decreased levels of one or more protein complexes can be diagnosed, or their suspected presence can be screened for, or a predisposition to develop such disorders can be detected, by detecting decreased levels of the one or more protein complexes, the mRNA encoding one or more members of the one or more complexes, or complex functional activity, or by detecting mutations in the component proteins that decrease complex formation, e.g., mutations such as translocations in nucleic acids, truncations in the gene or protein, changes in nucleotide or amino acid sequence relative to wild-type, that decrease complex formation.

Accordingly, in a specific embodiment of the invention, diseases and disorders involving aberrant compositions of the complexes can be diagnosed, or their suspected presence can be screened for, or a predisposition to develop such disorders can be detected, by detecting the component proteins of one or more complexes, or the mRNA encoding the members of the one or more complexes.

The use of detection techniques, especially those involving antibodies against a protein complex, provides a method of detecting specific cells that express the complex or component proteins. Using such assays, specific cell types can be defined in which one or more particular protein complexes are expressed, and the presence of the complex or component proteins can be correlated with cell viability, state, health, etc.

Also embodied are methods to detect a protein complex of the present invention in cell culture models that express particular protein complexes or derivatives thereof, for the purpose of characterizing or preparing the complexes for harvest. This embodiment includes cell sorting of prokaryotes such as but not restricted to bacteria (Davey and Kell, 1996, Microbiol. Rev. 60:641-696), primary cultures and tissue specimens from eukaryotes, including mammalian species such as human (Steele et al., 1996, Clin. Obstet. Gynecol 39:801-813), and continuous cell cultures (Orfao and Ruiz-Arguelles, 1996, Clin. Biochem. 29:5-9). Such isolations can be used as methods of diagnosis, described, supra.

In a further specific embodiment, a modulation of the formation process of a complex can be determined. Such a modulation can either be a change in the typical time course of its formation or a change in the typical steps leading to the formation of the complete complex.

Such changes can for example be detected by analysing and comparing the process of complex formation in untreated wild type cells of a particular type and/or cells showing or having the predisposition to develop a certain disease phenotype and/or cells which have been treated with particular conditions and/or particular agents in a particular situation.

Methods to study such changes in time course are well known in the art and include for example Western-blot analysis of the proteins in the complex isolated at different steps of its formation.

Furthermore an aberrant intracellular localization of the protein complex and/or an abberant transcription level of a gene dependent on the complex and/or the abundance and/or activity of a protein or protein complex dependent on the function of the complex and/or a gene dependent on the complex can serve as a marker for a disease and thus have diagnostic utility for any disease which is caused by an aberrant activity, function, composition or formation of the complex of the invention.

Methods to study the intracellular localization are well known in the art and include, but are not limited to immunofluorescence analysis using antibodies specific for components of the protein. Preferentially, double-stainings including staining of other cellular structures are being used to facilitate the detection of the intracellular localization. Methods to analyse the transcription levels of a gene dependent on the complex are also well known in the art and include Northern blot analysis, quantitative PCR etc. The abundance of proteins dependent on the protein can be analyzed as described supra. Methods to study changes in the activity of proteins dependent on complex depend on the protein. The choice of such methods will be apparent to any person skilled in the art.

4.4 THERAPEUTIC USES OF PROTEIN COMPLEXES/PROTEINS OF THE INVENTION

The present invention is directed to a method for treatment or prevention of various diseases and disorders by administration of a therapeutic compound (termed herein "therapeutic"). Such "therapeutics" include, but are not limited to, a protein complex of the present invention, the individual component proteins, and analogs and derivatives (including fragments) of the foregoing (e.g., as described hereinabove); antibodies thereto (as described hereinabove); nucleic acids encoding the component protein, and analogs or derivatives, thereof (e.g., as described hereinabove); component protein antisense nucleic acids, and agents that modulate complex formation and/or activity (i.e., agonists and antagonists).

The protein complexes as identified herein can be implicated in processes which are implicated in or associated with pathological conditions.

Diseases and disorders which can be treated and/or prevented and/or diagnosed by therapeutics interacting with any of the complexes provided herein are for example those listed in table 4.

These disorders are treated or prevented by administration of a therapeutic that modulates (i.e. inhibits or promotes) protein complex activity or formation or modulates its function or composition. Diseases or disorders associated with aberrant levels of complex activity or formation, or aberrant levels or activity of the component proteins, or aberrant complex composition or a change in the function, may be treated by administration of a therapeutic that modulates complex formation or activity or by the administration of a protein complex.

Therapeutics may also be administered to modulate complex formation or activity or level thereof in a microbial organism such as yeast, fungi such as Candida albicans causing an infectious disease in animals or humans.

Diseases and disorders characterized by increased (relative to a subject not suffering from the disease or disorder) complex levels or activity can be treated with therapeutics that antagonize (i.e., reduce or inhibit) complex formation or activity. Therapeutics that can be used include, but are not limited to, the component proteins or an analog, derivative or fragment of the component protein; anti-complex antibodies (e.g., antibodies specific for the protein complex, or a fragment or derivative of the antibody containing the binding region thereof; nucleic acids encoding the component proteins; antisense nucleic acids complementary to nucleic acids encoding the component proteins; and nucleic acids encoding the component protein that are dysfunctional due to, e.g., a heterologous insertion within the protein coding sequence, that are used to "knockout" endogenous protein function by homologous recombination, see, e.g., Capecchi, 1989, Science 244:1288-1292. In one embodiment, a therapeutic is 1 , 2 or more antisense nucleic acids which are complementary to 1 , 2, or more nucleic acids, respectfully, that encode component proteins of a complex.

In a specific embodiment of the present invention, a nucleic acid containing a portion of a component protein gene in which gene sequences flank (are both 5' and 3' to) a different gene sequence, is used as a component protein antagonist, or to promote component protein inactivation by homologous recombination (see also, Koller and Smithies, 1989, Proc. Natl. Acad. Sci. USA 86:8932-8935; Zijlstra et al., 1989, Nature 342: 435-438). Additionally, mutants or derivatives of a component protein that has greater affinity for another component protein or the complex than wild type may be administered to compete with wild type protein for binding, thereby reducing the levels of complexes containing the wild type protein. Other therapeutics that inhibit complex function can be identified by use of known convenient in vitro assays, e.g., based on their ability to inhibit complex formation, or as described in Section 4.5, infra.

In specific embodiments, therapeutics that antagonize complex formation or activity are administered therapeutically, including prophylactically, (1) in diseases or disorders involving an increased (relative to normal or desired) level of a complex, for example, in patients where complexes are overactive or overexpressed; or (2) in diseases or disorders where an in vitro (or in vivo) assay (see infra) indicates the utility of antagonist administration. Increased levels of a complex can be readily detected, e.g., by quantifying protein and/or RNA, by obtaining a patient tissue sample (e.g., from biopsy tissue) and assaying it in vitro for RNA or protein levels, or structure and/or activity of the expressed complex (or the encoding mRNA). Many methods standard in the art can be thus employed including, but not limited to, immunoassays to detect complexes and/or visualize complexes (e.g., Western blot analysis, immunoprecipitation followed by sodium dodecyl sulfate polyacrylamide gel electrophoresis [SDS-PAGE], immunocytochemistry, etc.), and/or hybridization assays to detect concurrent expression of component protein mRNA (e.g., Northern assays, dot blot analysis, in situ hybridization, etc.).

A more specific embodiment of the present invention is directed to a method of reducing complex expression (i.e., expression of the protein components of the complex and/or formation of the complex) by targeting mRNAs that express the protein moieties. RNA therapeutics currently fall within three classes, antisense species, ribozymes, or RNA aptamers (Good et al., 1997, Gene Therapy 4:45-54). Antisense oligonucleotides have been the most widely used. By way of example, but not limitation, antisense oligonucleotide methodology to reduce complex formation is presented below, infra. Ribozyme therapy involves the administration, induced expression, etc. of small RNA molecules with enzymatic ability to cleave, bind, or otherwise inactivate specific RNAs, to reduce or eliminate expression of particular proteins (Grassi and Marini, 1996, Annals of Medicine 28:499-510; Gibson, 1996, Cancer and Metastasis Reviews 15:287-299). RNA aptamers are specific RNA ligand proteins, such as for Tat and Rev RNA (Good et al., 1997, Gene Therapy 4:45-54) that can specifically inhibit their translation. Aptamers specific for component proteins can be identified by many methods well known in the art, for example, by affecting the formation of a complex in the protein-protein interaction assay described, infra.

In another embodiment, the activity or levels of a component protein are reduced by administration of another component protein, or the encoding nucleic acid, or an antibody that immunospecificaily binds to the component protein, or a fragment or a derivative of the antibody containing the binding domain thereof.

In another aspect of the invention, diseases or disorders associated with increased levels of an component protein of the complex may be treated or prevented by administration of a therapeutic that increases complex formation if the complex formation acts to reduce or inactivate the component protein through complex formation. Such diseases or disorders can be treated or prevented by administration of one component member of the complex, administration of antibodies or other molecules that stabilize the complex, etc.

Diseases and disorders associated with underexpression of a complex, or a component protein, are treated or prevented by administration of a therapeutic that promotes (i.e., increases or supplies) complex levels and/or function, or individual component protein function. Examples of such a therapeutic include but are not limited to a complex or a derivative, analog or fragment of the complex that are functionally active (e.g., able to form a complex), un-complexed component proteins and derivatives, analogs, and fragments of un-complexed component proteins, and nucleic acids encoding the members of a complex or functionally active derivatives or fragments of the members of the complex, e.g., for use in gene therapy. In a specific embodiment, a therapeutic includes derivatives, homologs or fragments of a component protein that increase and/or stabilize complex formation. Examples of other agonists can be identified using in vitro assays or animal models, examples of which are described, infra. In yet other specific embodiments of the present invention, therapeutics that promote complex function are administered therapeutically, including prophylactically, (1) in diseases or disorders involving an absence or decreased (relative to normal or desired) level of a complex, for example, in patients where a complex, or the individual components necessary to form the complex, is lacking, genetically defective, biologically inactive or underactive, or under-expressed; or (2) in diseases or disorders wherein an in vitro or in vivo assay (see, infra) indicates the utility of complex agonist administration. The absence or decreased level of a complex, component protein or function can be readily detected, e.g., by obtaining a patient tissue sample (e.g., from biopsy tissue) and assaying it in vitro for RNA or protein levels, structure and/or activity of the expressed complex and/or the concurrent expression of mRNA encoding the two components of the complex. Many methods standard in the art can be thus employed, including but not limited to immunoassays to detect and/or visualize a complex, or the individual components of a complex (e.g., Western blot analysis, immunoprecipitation followed by sodium dodecyl sulfate polyacrylamide gel electrophoresis [SDS-PAGE], immunocytochemistry, etc.) and/or hybridization assays to detect expression of mRNAs encoding the individual protein components of a complex by detecting and/or visualizing component mRNA concurrently or separately using, e.g., Northern assays, dot blot analysis, in situ hybridization, etc.

In specific embodiments, the activity or levels of a component protein are increased by administration of another component protein of the same complex, or a derivative, homolog or analog thereof, a nucleic acid encoding the other component, or an agent that stabilizes or enhances the other component, or a fragment or derivative of such an agent.

Generally, administration of products of species origin or species reactivity (in the case of antibodies) that is the same species as that of the patient is preferred. Thus, in a preferred embodiment, a human complex, or derivative, homolog or analog thereof; nucleic acids encoding the members of the human complex or a derivative, homolog or analog thereof; an antibody to a human complex, or a derivative thereof; or other human agents that affect component proteins or the complex, are therapeutically or prophylactically administered to a human patient.

Preferably, suitable in vitro or in vivo assays are utilized to determine the effect of a specific therapeutic and whether its administration is indicated for treatment of the affected tissue or individual. In various specific embodiments, in vitro assays can be carried out with representative cells of cell types involved in a patient's disorder, to determine if a therapeutic has a desired effect upon such cell types.

Compounds for use in therapy can be tested in suitable animal model systems prior to testing in humans, including, but not limited to, rats, mice, chicken, cows, monkeys, rabbits, etc. For in vivo testing, prior to administration to humans, any animal model system known in the art may be used. Additional descriptions and sources of therapeutics that can be used according to the invention are found in Sections 4.1 to 4.3 and 4.7 herein.

4.4.1 GENE THERAPY

In a specific embodiment of the present invention, nucleic acids comprising a sequence encoding the component proteins, or a functional derivative thereof, are administered to modulate complex activity or formation by way of gene therapy. Gene therapy refers to therapy performed by the administration of a nucleic acid to a subject. In this embodiment of the present invention, the nucleic acid expresses its encoded protein(s) that mediates a therapeutic effect by modulating complex activity or formation. Any of the methods for gene therapy available in the art can be used according to the present invention. Exemplary methods are described below.

For general reviews of the methods of gene therapy, see Goldspiel et al., 1993, Clinical Pharmacy 12:488-505; Wu and Wu, 1991 , Biotherapy 3:87-95; Tolstoshev, 1993, Ann. Rev. Pharmacol. Toxicol. 32:573-596; Mulligan, 1993, Science 260:926-932; Morgan and Anderson, 1993, Ann. Rev. Biochem. 62:191-217; and May, 1993, TIBTECH 11 :155-215. Methods commonly known in the art of recombinant DNA technology which can be used are described in Ausubel et al., eds., 1993, Current Protocols in Molecular Biology, John Wiley & Sons, NY; and Kriegler, 1990, Gene Transfer and Expression, A Laboratory Manual, Stockton Press, NY.

In a preferred aspect, the therapeutic comprises a nucleic acid that is part of an expression vector that expresses one or more of the component proteins, or fragments or chimeric proteins thereof, in a suitable host. In particular, such a nucleic acid has a promoter operably linked to the protein coding region(s) (or, less preferably separate promoters linked to the separate coding regions separately), said promoter being inducible or constitutive, and optionally, tissue-specific. In another particular embodiment, a nucleic acid molecule is used in which the coding sequences, and any other desired sequences, are flanked by regions that promote homologous recombination at a desired site in the genome, thus providing for intra-chromosomal expression of the component protein nucleic acids (Koller and Smithies, 1989, Proc. Natl. Acad. Sci. USA 86:8932-8935; Zijlstra et al., 1989, Nature 342:435-438).

Delivery of the nucleic acid into a patient may be either direct, in which case the patient is directly exposed to the nucleic acid or nucleic acid-carrying vector, or indirect, in which case, cells are first transformed with the nucleic acid in vitro, then transplanted into the patient. These two approaches are known, respectively, as in vivo or ex vivo gene therapy.

In a specific embodiment, the nucleic acid is directly administered in vivo, where it is expressed to produce the encoded product. This can be accomplished by any of numerous methods known in the art, e.g., by constructing it as part of an appropriate nucleic acid expression vector and administering it so that it becomes intracellular, e.g., by infection using a defective or attenuated retroviral or other viral vector (U.S. Patent No. 4,980,286), or by direct injection of naked DNA, or by use of microparticle bombardment (e.g., a gene gun; Biolistic, Dupont), or coating with lipids or cell-surface receptors, or through use of transfecting agents, by encapsulation in liposomes, microparticles, or microcapsules, or by administering it in linkage to a peptide that is known to enter the nucleus, or by administering it in linkage to a ligand subject to receptor-mediated endocytosis that can be used to target cell types specifically expressing the receptors (e.g., Wu and Wu, 1987, J. Biol. Chem. 262:4429-4432), etc. In another embodiment, a nucleic acid-ligand complex can be formed in which the ligand comprises a fusogenic viral peptide that disrupts endosomes, allowing the nucleic acid to avoid lysosomal degradation. In yet another embodiment, the nucleic acid can be targeted in vivo for cell specific uptake and expression, by targeting a specific receptor (see, e.g., International Patent Publications WO 92/06180; WO 92/22635; WO 92/20316; WO 93/14188; and WO 93/20221. Alternatively, the nucleic acid can be introduced intracellularly and incorporated within host cell DNA for expression, by homologous recombination (Koller and Smithies, 1989, Proc. Natl. Acad. Sci. USA 86:8932-8935; Zijlstra et al., 1989, Nature 342:435-438).

In a specific embodiment, a viral vector that contains the component protein encoding nucleic acids is used. For example, a retroviral vector can be used (Miller et al., 1993, Meth. Enzymol. 217:581-599). These retroviral vectors have been modified to delete retroviral sequences that are not necessary for packaging of the viral genome and integration into host cell DNA. The encoding nucleic acids to be used in gene therapy is/are cloned into the vector, which facilitates delivery of the gene into a patient. More detail about retroviral vectors can be found in Boesen et al., 1994, Biotherapy 6:291-302, which describes the use of a retroviral vector to deliver the mdrl gene to hematopoetic stem cells in order to make the stem cells more resistant to chemotherapy. Other references illustrating the use of retroviral vectors in gene therapy are Clowes et al., 1994, J. Clin. Invest. 93:644-651 ; Kiem et al., 1994, Blood 83:1467-1473; Salmons and Gunzberg, 1993, Human Gene Therapy 4:129-141 ; and Grossman and Wilson, 1993, Curr. Opin. in Genetics and Devel. 3:110-114.

Adenoviruses are other viral vectors that can be used in gene therapy. Adenoviruses are especially attractive vehicles for delivering genes to respiratory epithelia. Adenoviruses naturally infect respiratory epithelia where they cause a mild disease. Other targets for adenovirus-based delivery systems are the liver, the central nervous system, endothelial cells and muscle. Adenoviruses have the advantage of being capable of infecting non-dividing cells. Kozarsky and Wilson, 1993, Curr. Opin. Genet. Devel. 3:499-503, discuss adenovirus-based gene therapy. The use of adenovirus vectors to transfer genes to the respiratory epithelia of rhesus monkeys has been demonstrated by Bout et al., 1994, Human Gene Therapy 5:3-10. Other instances of the use of adenoviruses in gene therapy can be found in Rosenfeld et al., 1991 , Science 252:431-434; Rosenfeld et al., 1992, Cell 68:143-155; and Mastrangeli et al., 1993, J. Clin. Invest. 91 :225-234.

Adeno-associated virus (AAV) has also been proposed for use in gene therapy (Walsh et al., 1993, Proc. Soc. Exp. Biol. Med. 204:289-300.

Another approach to gene therapy involves transferring a gene into cells in tissue culture by methods such as electroporation, lipofection, calcium phosphate-mediated transfection, or viral infection. Usually, the method of transfer includes the transfer of a selectable marker to the cells. The cells are then placed under selection to isolate those cells that have taken up and are expressing the transferred gene from these that have not. Those cells are then delivered to a patient.

In this embodiment, the nucleic acid is introduced into a cell prior to administration in vivo of the resulting recombinant cell. Such introduction can be carried out by any method known in the art including, but not limited to, transfection by electroporation, microinjection, infection with a viral or bacteriophage vector containing the nucleic acid sequences, cell fusion, chromosome-mediated gene transfer, microcell-mediated gene transfer, spheroplast fusion, etc. Numerous techniques are known in the art for the introduction of foreign genes into cells (see, e.g., Loeffler and Behr, 1993, Meth. Enzymol. 217:599-618; Cohen et al., 1993, Meth. Enzymol. 217:618-644; Cline, 1985, Pharmac. Ther. 29:69-92) and may be used in accordance with the present invention, provided that the necessary developmental and physiological functions of the recipient cells are not disrupted. The technique should provide for the stable transfer of the nucleic acid to the cell, so that the nucleic acid is expressible by the cell and preferably, is heritable and expressible by its cell progeny.

The resulting recombinant cells can be delivered to a patient by various methods known in the art. In a preferred embodiment, epithelial cells are injected, e.g., subcutaneously. In another embodiment, recombinant skin cells may be applied as a skin graft onto the patient. Recombinant blood cells (e.g., hematopoetic stem or progenitor cells) are preferably administered intravenously. The amount of cells envisioned for use depends on the desired effect, patient state, etc., and can be determined by one skilled in the art.

Cells into which a nucleic acid can be introduced for purposes of gene therapy encompass any desired, available cell type, and include but are not limited to epithelial cells, endothelial cells, keratinocytes, fibroblasts, muscle cells, hepatocytes, blood cells such as T lymphocytes, B lymphocytes, monocytes, macrophages, neutrophils, eosinophils, megakaryocytes, and granulocytes, various stem or progenitor cells, in particular hematopoetic stem or progenitor cells, e.g., as obtained from bone marrow, umbilical cord blood, peripheral blood, fetal liver, etc.

In a preferred embodiment, the cell used for gene therapy is autologous to the patient.

In an embodiment in which recombinant cells are used in gene therapy, a component protein encoding nucleic acid is/are introduced into the cells such that the gene or genes are expressible by the cells or their progeny, and the recombinant cells are then administered in vivo for therapeutic effect. In a specific embodiment, stem or progenitor cells are used. Any stem and/or progenitor cells which can be isolated and maintained in vitro can potentially be used in accordance with this embodiment of the present invention. Such stem cells include but are not limited to hematopoetic stem cells (HSCs), stem cells of epithelial tissues such as the skin and the lining of the gut, embryonic heart muscle cells, liver stem cells (International Patent Publication WO 94/08598), and neural stem cells (Stemple and Anderson, 1992, Cell 71 :973-985).

Epithelial stem cells (ESCs), or keratinocytes, can be obtained from tissues such as the skin and the lining of the gut by known procedures (Rheinwald, 1980, Meth. Cell Biol. 2A:229). In stratified epithelial tissue such as the skin, renewal occurs by mitosis of stem cells within the germinal layer, the layer closest to the basal lamina. Similarly, stem cells within the lining of the gut provide for a rapid renewal rate of this tissue. ESCs or keratinocytes obtained from the skin or lining of the gut of a patient or donor can be grown in tissue culture (Rheinwald, 1980, Meth. Cell Bio. 2A:229; Pittelkow and Scott, 1986, Mayo Clinic Proc. 61 :771). If the ESCs are provided by a donor, a method for suppression of host versus graft reactivity (e.g., irradiation, or drug or antibody administration to promote moderate immunosuppression) can also be used.

With respect to hematopoetic stem cells (HSCs), any technique that provides for the isolation, propagation, and maintenance in vitro of HSCs can be used in this embodiment of the invention. Techniques by which this may be accomplished include (a) the isolation and establishment of HSC cultures from bone marrow cells isolated from the future host, or a donor, or (b) the use of previously established long-term HSC cultures, which may be allogeneic or xenogeneic. Non-autologous HSCs are used preferably in conjunction with a method of suppressing transplantation immune reactions between the future host and patient. In a particular embodiment of the present invention, human bone marrow cells can be obtained from the posterior iliac crest by needle aspiration (see, e.g., Kodo et al., 1984, J. Clin. Invest. 73: 1377-1384). In a preferred embodiment of the present invention, the HSCs can be made highly enriched or in substantially pure form. This enrichment can be accomplished before, during, or after long-term culturing, and can be done by any technique known in the art. Long-term cultures of bone marrow cells can be established and maintained by using, for example, modified Dexter cell culture techniques (Dexter et al., 1977, J. Cell Physiol. 91 :335) or Witlock-Witte culture techniques (Witlock and Witte, 1982, Proc. Natl. Acad. Sci. USA 79:3608-3612).

In a specific embodiment, the nucleic acid to be introduced for purposes of gene therapy comprises an inducible promoter operably linked to the coding region, such that expression of the nucleic acid is controllable by controlling the presence or absence of the appropriate inducer of transcription. Additional methods can be adapted for use to deliver a nucleic acid encoding the component proteins, or functional derivatives thereof, e.g., as described in Section 4.1 , supra.

4.4.2 USE OF ANTISENSE OLIGONUCLEOTIDES FOR SUPPRESSION OF PROTEIN COMPLEX FORMATION OR PROTEIN COMPLEX/PROTEIN ACTIVITY

In a specific embodiment of the present invention, protein complex activity and formation and protein activity is inhibited by use of antisense nucleic acids for the component proteins of the complex, that inhibit transcription and/or translation of their complementary sequence. The present invention provides the therapeutic or prophylactic use of nucleic acids of at least six nucleotides that are antisense to a gene or cDNA encoding a component protein, or a portion thereof. An "antisense" nucleic acid as used herein refers to a nucleic acid capable of hybridizing to a sequence-specific portion of a component protein RNA (preferably mRNA) by virtue of some sequence complementarity. The antisense nucleic acid may be complementary to a coding and/or noncoding region of a component protein mRNA. Such antisense nucleic acids that inhibit complex formation or activity have utility as therapeutics, and can be used in the treatment or prevention of disorders as described supra.

The antisense nucleic acids of the invention can be oligonucleotides that are double-stranded or single-stranded, RNA or DNA, or a modification or derivative thereof, which can be directly administered to a cell, or which can be produced intracellularly by transcription of exogenous, introduced sequences.

In another embodiment, the present invention is directed to a method for inhibiting the expression of component protein nucleic acid sequences, in a prokaryotic or eukaryotic cell, comprising providing the cell with an effective amount of a composition comprising an antisense nucleic acid of the component protein, or a derivative thereof, of the invention.

The antisense nucleic acids are of at least six nucleotides and are preferably oligonucleotides, ranging from 6 to about 200 nucleotides. In specific aspects, the oligonucleotide is at least 10 nucleotides, at least 15 nucleotides, at least 100 nucleotides, or at least 200 nucleotides. The oligonucleotides can be DNA or RNA or chimeric mixtures, or derivatives or modified versions thereof, and either single-stranded or double-stranded. The oligonucleotide can be modified at the base moiety, sugar moiety, or phosphate backbone. The oligonucleotide may include other appending groups such as peptides, agents facilitating transport across the cell membrane (see, e.g., Letsinger et al., 1989, Proc. Natl. Acad. Sci. USA 86:6553-6556; Lemaitre et al., 1987, Proc. Natl. Acad. Sci. USA 84:648-652; International Patent Publication No. WO 88/09810) or blood-brain barrier (see, e.g., International Patent Publication No. WO 89/10134), hybridization-triggered cleavage agents (see, e.g., Krol et al., 1988, BioTechniques 6:958-976), or intercalating agents (see, e.g., Zon, 1988, Pharm. Res. 5:539-549).

In a preferred aspect of the invention, an antisense oligonucleotide is provided, preferably as single-stranded DNA. The oligonucleotide may be modified at any position in its structure with constituents generally known in the art.

The antisense oligonucleotides may comprise at least one modified base moiety which is selected from the group including but not limited to 5-fluorouracil, 5-bromouracil, 5-chlorouracil, 5-iodouracil, hypoxanthine, xanthine, 4-acetylcytosine, 5-(carboxyhydroxylmethyl)uracil, 5-carboxymethylaminomethyl-2-thio-uridine,

5-carboxymethylaminomethyluracil, dihydrouracil, β-D-galactosylqueosine, inosine, N6-isopentenyladenine, 1-methylguanine, 1-methylinosine, 2,2-dimethylguanine, 2-methyladenine, 2-methylguanine, 3-methylcytosine, 5-methylcytosine, N6-adenine, 7-methylguanine, 5-methylaminomethyluracil, 5-methoxyaminomethyl-2-thiouracil, β-D-mannosylqueosine, 5N-methoxycarboxymethyluracil, 5-methoxyuracil, 2-methyl- thio-N6-isopentenyladenine, uracil-5-oxyacetic acid (v), wybutoxosine, pseudouracil, queosine, 2-thiocytosine, 5-methyl-2-thiouracil, 2-thiouracil, 4-thiouracil, 5-methyluracil, uracil-5-oxyacetic acid methylester, uracil-5-oxyacetic acid (v), 5-methyl-2-thiouracil, 3-(3-amino-3-N-2-carboxypropyl) uracil, (acp3)w, and 2,6-diaminopurine.

In another embodiment, the oligonucleotide comprises at least one modified sugar moiety selected from the group including, but not limited to, arabinose, 2-fluoroarabinose, xylulose, and hexose.

In yet another embodiment, the oligonucleotide comprises at least one modified phosphate backbone selected from the group consisting of a phosphorothioate, a phosphorodithioate, a phosphoramidothioate, a phosphoramidate, a phosphordiamidate, a methylphosphonate, an alkyl phosphotriester, and a formacetal, or an analog of the foregoing. In yet another embodiment, the oligonucleotide is a 2-a-anomeric oligonucleotide. An a-anomeric oligonucleotide forms specific double-stranded hybrids with complementary RNA in which, contrary to the usual β-units, the strands run parallel to each other (Gautier et al., 1987, Nucl. Acids Res. 15:6625-6641).

The oligonucleotide may be conjugated to another molecule, e.g., a peptide, hybridization-triggered cross-linking agent, transport agent, hybridization-triggered cleavage agent, etc.

Oligonucleotides of the invention may be synthesized by standard methods known in the art, e.g., by use of an automated DNA synthesizer (such as are commercially avail-able from Biosearch, Applied Biosystems, etc.). As examples, phosphorothioate oligo-nucleotides may be synthesized by the method of Stein et al. (1988, Nucl. Acids Res. 16:3209), methylphosphonate oligonucleotides can be prepared by use of controlled pore glass polymer supports (Sarin et al., 1988, Proc. Natl. Acad. Sci. USA 85:7448-7451), etc.

In a specific embodiment, the antisense oligonucleotides comprise catalytic RNAs, or ribozymes (see, e.g., International Patent Publication No. WO 90/11364; Sarver et al., 1990, Science 247:1222-1225). In another embodiment, the oligonucleotide is a 2'-0-methylribonucleotide (Inoue et al., 1987, Nucl. Acids Res. 15:6131-6148), or a chimeric RNA-DNA analog (Inoue et al., 1987, FEBS Lett. 215:327- 330).

In an alternative embodiment, the antisense nucleic acids of the invention are produced intracellularly by transcription from an exogenous sequence. For example, a vector can be introduced in vivo such that it is taken up by a cell, within which cell the vector or a portion thereof is transcribed, producing an antisense nucleic acid (RNA) of the invention. Such a vector would contain a sequence encoding the component protein. Such a vector can remain episomal or become chromosomaliy integrated, as long as it can be transcribed to produce the desired antisense RNA. Such vectors can be constructed by recombinant DNA technology methods standard in the art. Vectors can be plasmid, viral, or others known in the art to be capable of replication and expression in mammalian cells. Expression of the sequences encoding the antisense RNAs can be by any promoter known in the art to act in mammalian, preferably human, cells. Such promoters can be inducible or constitutive. Such promoters include, but are not limited to, the SV40 early promoter region (Bemoist and Chambon, 1981 , Nature 290:304-310), the promoter contained in the 3' long terminal repeat of Rous sarcoma virus (Yamamoto et al., 1980, Cell 22:787-797), the herpes thymidine kinase promoter (Wagner et al., 1981 , Proc. Natl. Acad. Sci. USA 78:1441-1445), the regulatory sequences of the metallothionein gene (Brinster et al., 1982, Nature 296:39-42), etc.

The antisense nucleic acids of the invention comprise a sequence complementary to at least a portion of an RNA transcript of a component protein gene, preferably a human gene. However, absolute complementarity, although preferred, is not required. A sequence "complementary to at least a portion of an RNA," as referred to herein, means a sequence having sufficient complementarity to be able to hybridize with the RNA, forming a stable duplex; in the case of double-stranded antisense nucleic acids, a single strand of the duplex DNA may thus be tested, or triplex formation may be assayed. The ability to hybridize will depend on both the degree of complementarity and the length of the antisense nucleic acid. Generally, the longer the hybridizing nucleic acid, the more base mismatches with a component protein RNA it may contain and still form a stable duplex (or triplex, as the case may be). One skilled in the art can ascertain a tolerable degree of mismatch by use of standard procedures to determine the melting point of the hybridized complex.

The component protein antisense nucleic acids can be used to treat (or prevent) disorders of a cell type that expresses, or preferably overexpresses, a protein complex.

Cell types that express or overexpress component protein RNA can be identified by various methods known in the art. Such methods include, but are not limited to, hybridization with component protein-specific nucleic acids (e.g., by Northern blot hybridization, dot blot hybridization, or in situ hybridization), or by observing the ability of RNA from the cell type to be translated in vitro into the component protein by immunohistochemistry, Western blot analysis, ELISA, etc. In a preferred aspect, primary tissue from a patient can be assayed for protein expression prior to treatment, e.g., by immunocytochemistry, in situ hybridization, or any number of methods to detect protein or mRNA expression.

Pharmaceutical compositions of the invention (see Section 4.7, infra), comprising an effective amount of a protein component antisense nucleic acid in a pharmaceutically acceptable carrier can be administered to a patient having a disease or disorder that is of a type that expresses or overexpresses a protein complex of the present invention.

The amount of antisense nucleic acid that will be effective in the treatment of a particular disorder or condition will depend on the nature of the disorder or condition, and can be determined by standard clinical techniques. Where possible, it is desirable to determine the antisense cytotoxicity in vitro, and then in useful animal model systems, prior to testing and use in humans.

In a specific embodiment, pharmaceutical compositions comprising antisense nucleic acids are administered via liposomes, microparticles, or microcapsules. In various embodiments of the invention, it may be useful to use such compositions to achieve sustained release of the antisense nucleic acids. In a specific embodiment, it may be desirable to utilize liposomes targeted via antibodies to specific identifiable central nervous system cell types (Leonetti et al., 1990, Proc. Natl. Acad. Sci. U.S.A. 87:2448-2451; Renneisen et al., 1990, J. Biol. Chem. 265:16337-16342).

4.5 ASSAYS OF PROTEIN COMPLEXES/PROTEINS OF THE INVENTION AND DERIVATIVES AND ANALOGS THEREOF

The functional activity of a protein complex of the present invention, or a derivative, fragment or analog thereof or protein component thereof, can be assayed by various methods. Potential modulators (e.g., agonists and antagonists) of complex activity or formation, e.g., anti- complex antibodies and antisense nucleic acids, can be assayed for the ability to modulate complex activity or formation.

In one embodiment of the present invention, where one is assaying for the ability to bind or compete with a wild-type complex for binding to an anti-complex antibody, various immunoassays known in the art can be used, including but not limited to competitive and non-competitive assay systems using techniques such as radioimmunoassay, ELISA (enzyme linked immunosorbent assay), "sandwich" immunoassays, immunoradiometric assays, gel diffusion precipitin reactions, immunodiffusion assays, in situ immunoassays (using colloidal gold, enzyme or radioisotope labels), western blot analysis, precipitation reactions, agglutination assays (e.g., gel agglutination assays, hemagglutination assays), complement fixation assays, immunofluorescence assays, protein A assays, immunoelectrophoresis assays, etc. In one embodiment, antibody binding is detected by detecting a label on the primary antibody. In another embodiment, the primary antibody is detected by detecting binding of a secondary antibody or reagent to the primary antibody. In a further embodiment, the secondary antibody is labeled. Many means are known in the art for detecting binding in an immunoassay and are within the scope of the present invention. The expression of the component protein genes (both endogenous and those expressed from cloned DNA containing the genes) can be detected using techniques known in the art, including but not limited to Southern hybridization (Southern, 1975, J. Mol. Biol. 98:503-517), northern hybridization (see, e.g., Freeman et al., 1983, Proc. Natl. Acad. Sci. USA 80:4094-4098), restriction endonuclease mapping (Sambrook et al., 1989, Molecular Cloning, A Laboratory Manual, 2^nd Ed. Cold Spring Harbor Laboratory Press, New York), RNase protection assays (Current Protocols in Molecular Biology, John Wiley and Sons, New York, 1997), DNA sequence analysis, and polymerase chain reaction amplification (PCR; U.S. Patent Nos. 4,683,202, 4,683,195, and 4,889,818; Gyllenstein et al., 1988, Proc. Natl. Acad. Sci. USA 85:7652-7657; Ochman et al., 1988, Genetics 120:621-623; Loh et al., 1989, Science 243:217-220) followed by Southern hybridization with probes specific for the component protein genes, in various cell types. Methods of amplification other than PCR commonly known in the art can be employed. In one embodiment, Southern hybridization can be used to detect genetic linkage of component protein gene mutations to physiological or pathological states. Various cell types, at various stages of development, can be characterized for their expression of component proteins at the same time and in the same cells. The stringency of the hybridization conditions for northern or Southern blot analysis can be manipulated to ensure detection of nucleic acids with the desired degree of relatedness to the specific probes used. Modifications to these methods and other methods commonly known in the art can be used.

Derivatives (e.g., fragments), homologs and analogs of one component protein can be assayed for binding to another component protein in the same complex by any method known in the art, for example the modified yeast matrix mating test described in Section 4.6.1 infra, immunoprecipitation with an antibody that binds to the component protein complexed with other component proteins in the same complex, followed by size fractionation of the immunoprecipitated. proteins (e.g., by denaturing or nondenaturing polyacrylamide gel electrophoresis), Western blot analysis, etc.

One embodiment of the invention provides a method for screening a derivative, homolog or analog of a component protein for biological activity comprising contacting said derivative, homolog or analog of the component protein with the other component proteins in the same complex; and detecting the formation of a complex between said derivative, homolog or analog of the component protein and the other component proteins; wherein detecting formation of said complex indicates that said derivative, homolog or analog of has biological (e.g., binding) activity.

The invention also provides methods of modulating the activity of a component protein that can participate in a protein complex by administration of a binding partner of that protein or derivative, homolog or analog thereof.

In a specific embodiment of the present invention, a protein complex of the present invention is administered to treat or prevent a disease or disorder, since the complex and/or component proteins have been implicated in the disease and disorder. Accordingly, a protein complex or a derivative, homolog, analog or fragment thereof, nucleic acids encoding the component proteins, anti-complex antibodies, and other modulators of protein complex activity, can be tested for activity in treating or preventing a disease or disorder in in vitro and in vivo assays.

In one embodiment, a therapeutic of the invention can be assayed for activity in treating or preventing a disease by contacting cultured cells that exhibit an indicator of the disease in vitro, with the therapeutic, and comparing the level of said indicator in the cells contacted with the therapeutic, with said level of said indicator in cells not so contacted, wherein a lower level in said contacted cells indicates that the therapeutic has activity in treating or preventing the disease.

In another embodiment of the invention, a therapeutic of the invention can be assayed for activity in treating or preventing a disease by administering the therapeutic to a test animal that is predisposed to develop symptoms of a disease, and measuring the change in said symptoms of the disease after administration of said therapeutic, wherein a reduction in the severity of the symptoms of the disease or prevention of the symptoms of the disease indicates that the therapeutic has activity in treating or preventing the disease. Such a test animal can be any one of a number of animal models known in the art for disease. These animal models are well known in the art. These animal models include, but are not limited to those which are listed in the section 4.6 (supra) as exemplary animal models to study any of the complexes provided in the invention.

4.6 SCREENING FOR MODULATORS OF THE PROTEIN COMPLEXES/PROTEINS OF THE INVENTION A complex of the present invention, the component proteins of the complex and nucleic acids encoding the component proteins, as well as derivatives and fragments of the amino and nucleic acids, can be used to screen for compounds that bind to, or modulate the amount of, activity of, or protein component composition of, said complex, and thus, have potential use as modulators, i.e., agonists or antagonists, of complex activity, and/or complex formation, i.e., the amount of complex formed, and/or protein component composition of the complex.

Thus, the present invention is also directed to methods for screening for molecules that bind to, or modulate the function of, amount of, activity of, formation of or protein component composition of, a complex of the present invention. In one embodiment of the invention, the method for screening for a molecule that modulates directly or indirectly the function, activity or formation of a complex of the present invention comprises exposing said complex, or a cell or organism containing the complex machinery, to one or more candidate molecules under conditions conducive to modulation; and determining the amount of, the biochemical activity of, protein components of, and/or intracellular localization of, said complex and/or the transcription level of a gene dependend on the complex and/or the abundance and/or activity of a protein or protein complex dependend on the function of the complex and/or product of a gene dependent on the complex in the presence of the one or more candidate molecules, wherein a change in said amount, activity, protein components or intracellular localization relative to said amount, activity, protein components and/or intracellular localization and/or a change in the transcription level of a gene dependend on the complex and/or the abundance and/or activity of a protein or protein complex dependent on the function of the complex and/or product of a gene dependent on the complex in the absence of said candidate molecules indicates that the molecule modulates function, activity or composition of said complex.

In a further specific embodiment, a modulation of the formation process of a complex can be determined.

Such a modulation can either be a change in the typical time course of its formation or a change in the typical steps leading to the formation of the complete complex.

Such changes can for example be detected by analysing and comparing the process of complex formation in untreated wild type cells of a particular type and/or cells showing or having the predisposition to develop a certain disease phenotype and/or cells which have been treated with particular conditions and/or particular agents in a particular situation. Methods to study such changes in time course are well known in the art and include for example Western-blot analysis of the proteins in the complex isolated at different steps of its formation.

Methods to study the intracellular localization are well known in the art and include, but are not limited to immunofluorescence analysis using antibodies specific for components of the protein. Preferentially, double-stainings including staining of other cellular structures are being used to facilitate the detection of the intracellular localization. Methods to analyse the transcription levels of a gene dependent on the complex are also well known in the art and include Northern blot analysis, quantitative PCR etc. The abundance of proteins dependent on the protein can be analyzed as described supra. Methods to study changes in the activity of proteins dependent on complex depend on the protein. The. choice of such methods will be apparent to any person skilled in the art.

In another embodiment, the present invention further relates to a process for the identification and/or preparation of an effector of the complex comprising the step of bringing into contact a product of any of claims 1 to 8 with a compound, a mixture or a library of compounds and determining whether the compound or a certain compound of the mixture or library binds to the product and/or effects the products biological activity and optionally further purifying the compound positively tested as effector.

In another embodiment, the present invention is directed to a method for screening for a molecule that binds a protein complex of the present invention comprising exposing said complex, or a cell or organism containing the complex machinery, to one or more candidate molecules; and determining whether said complex is bound by any of said candidate molecules. Such screening assays can be carried out using cell-free and cell-based methods that are commonly known in the art in vitro, in vivo or ex vivo. For example, an isolated complex can be employed, or a cell can be contacted with the candidate molecule and the complex can be isolated from such contacted cells and the isolated complex can be assayed for activity or component composition. In another example, a cell containing the complex can be contacted with the candidate molecule and the levels of the complex in the contacted cell can be measured. Additionally, such assays can be carried out in cells recombinantly expressing a component protein from the fourth column of table 1 , or a functionally active fragment or functionally active derivative thereof, and a component protein from fifth column of table 1 , or a functionally active fragment or functionally active derivative thereof. Additionally, such assays can also be carried out in cells recombinantly expressing all component proteins from the group of proteins in the fifth column of table 1.

For example, assays can be carried out using recombinant cells expressing the protein components of a complex, to screen for molecules that bind to, or interfere with, or promote complex activity or formation. In preferred embodiments, polypeptide derivatives that have superior stabilities but retain the ability to form a complex (e.g., one or more component proteins modified to be resistant to proteolytic degradation in the binding assay buffers, or to be resistant to oxidative degradation), are used to screen for modulators of complex activity or formation. Such resistant molecules can be generated, e.g., by substitution of amino acids at proteolytic cleavage sites, the use of chemically derivatized amino acids at proteolytic susceptible sites, and the replacement of amino acid residues subject to oxidation, i.e. methionine and cysteine.

A particular aspect of the present invention relates to identifying molecules that inhibit or promote formation or degradation of a complex of the present invention, e.g., using the method described for isolating the complex and identifying members of the complex using the TAP assay described in Section 4, infra, and in WO 00/09716 and Rigaut et al., 1999, Nature Biotechnol. 17:1030-1032, which are each incorporated by reference in their entirety. TNRF1

In another embodiment of the invention, a modulator is identified by administering a candidate molecule to a transgenic non-human animal expressing the complex component proteins from promoters that are not the native promoters of the respective proteins, more preferably where the candidate molecule is also recombinantly expressed in the transgenic non-human animal. Alternatively, the method for identifying such a modulator can be carried out in vitro, preferably with a purified complex, and a purified candidate molecule. Agents/molecules (candidate molecules) to be screened can be provided as mixtures of a limited number of specified compounds, or as compound libraries, peptide libraries and the like. Agents/molecules to be screened may also include all forms of antisera, antisense nucleic acids, etc., that can modulate complex activity or formation. Exemplary candidate molecules and libraries for screening are set forth in Section 4.6.1 , infra.

Screening the libraries can be accomplished by any of a variety of commonly known methods. See, e.g., the following references, which disclose screening of peptide libraries: Parmley and Smith, 1989, Adv. Exp. Med. Biol. 251 :215-218; Scott and Smith, 1990, Science 249:386-390; Fowlkes et al., 1992, BioTechniques 13:422-427; Oldenburg et al., 1992, Proc. Natl. Acad. Sci. USA 89:5393-5397; Yu et al., 1994, Cell 76:933-945; Staudt et al., 1988, Science 241 :577-580; Bock et al., 1992, Nature 355:564-566; Tuerk et al., 1992, Proc. Natl. Acad. Sci. USA 89:6988-6992; Ellington et al., 1992, Nature 355:850-852; U.S. Patent No. 5,096,815, U.S. Patent No. 5,223,409, and U.S. Patent No. 5,198,346, all to Ladner et al.; Rebar and Pabo, 1993, Science 263:671-673; and International Patent Publication No. WO 94/18318.

In a specific embodiment, screening can be carried out by contacting the library members with a complex immobilized on a solid phase, and harvesting those library members that bind to the protein (or encoding nucleic acid or derivative). Examples of such screening methods, termed "panning" techniques, are described by way of example in Parmley and Smith, 1988, Gene 73:305-318; Fowlkes et al., 1992, BioTechniques 13:422-427; International Patent Publication No. WO 94/18318; and in references cited hereinabove.

In a specific embodiment, fragments and/or analogs of protein components of a complex, especially peptidomimetics, are screened for activity as competitive or non- competitive inhibitors of complex formation (amount of complex or composition of complex) or activity in the cell, which thereby inhibit complex activity or formation in the cell.

In one embodiment, agents that modulate (i.e., antagonize or agonize) complex activity or formation can be screened for using a binding inhibition assay, wherein agents are screened for their ability to modulate formation of a complex under aqueous, or physiological, binding conditions in which complex formation occurs in the absence of the agent to be tested. Agents that interfere with the formation of complexes of the invention are identified as antagonists of complex formation. Agents that promote the formation of complexes are identified as agonists of complex formation. Agents that completely block the formation of complexes are identified as inhibitors of complex formation.

Methods for screening may involve labeling the component proteins of the complex with radioligands (e.g., ¹²⁵l or ³H), magnetic ligands (e.g., paramagnetic beads covalently attached to photobiotin acetate), fluorescent ligands (e.g., fluorescein or rhodamine), or enzyme ligands (e.g., luciferase or β-galactosidase). The reactants that bind in solution can then be isolated by one of many techniques known in the art, including but not restricted to, co-immunoprecipitation of the labeled complex moiety using antisera against the unlabeled binding partner (or labeled binding partner with a distinguishable marker from that used on the second labeled complex moiety), immunoaffinity chromatography, size exclusion chromatography, and gradient density centrifugation. In a preferred embodiment, the labeled binding partner is a small fragment or peptidomimetic that is not retained by a commercially available filter. Upon binding, the labeled species is then unable to pass through the filter, providing for a simple assay of complex formation.

Methods commonly known in the art are used to label at least one of the component members of the complex. Suitable labeling methods include, but are not limited to, radiolabeling by incorporation of radiolabeled amino acids, e.g., ³H-leucine or ³⁵S-methionine, radiolabeling by post-translational iodination with ¹²⁵l or ¹³¹l using the chloramine T method, Bolton-Hunter reagents, etc., or labeling with ³²P using phosphorylase and inorganic radiolabeled phosphorous, biotin labeling with photobiotin- acetate and sunlamp exposure, etc. In cases where one of the members of the complex is immobilized, e.g., as described infra, the free species is labeled. Where neither of the interacting species is immobilized, each can be labeled with a distinguishable marker such that isolation of both moieties can be followed to provide for more accurate quantification, and to distinguish the formation of homomeric from heteromeric complexes. Methods that utilize accessory proteins that bind to one of the modified interactants to improve the sensitivity of detection, increase the stability of the complex, etc., are provided.

Typical binding conditions are, for example, but not by way of limitation, in an aqueous salt solution of 10-250 mM NaCI, 5-50 M Tris-HCI, pH 5-8, and 0.5% Triton X- 100 or other detergent that improves specificity of interaction. Metal chelators and/or divalent cations may be added to improve binding and/or reduce proteolysis. Reaction temperatures may include 4, 10, 15, 22, 25, 35, or 42 degrees Celsius, and time of incubation is typically at least 15 seconds, but longer times are preferred to allow binding equilibrium to occur. Particular complexes can be assayed using routine protein binding assays to determine optimal binding conditions for reproducible binding.

The physical parameters of complex formation can be analyzed by quantification of complex formation using assay methods specific for the label used, e.g., liquid scintillation counting for radioactivity detection, enzyme activity for enzyme-labeled moieties, etc. The reaction results are then analyzed utilizing Scatchard analysis, Hill analysis, and other methods commonly known in the arts (see, e.g., Proteins, Structures, and Molecular Principles, 2^nd Edition (1993) Creighton, Ed., W.H. Freeman and Company, New York).

In a second common approach to binding assays, one of the binding species is immobilized on a filter, in a microtiter plate well, in a test tube, to a chromatography matrix, etc., either covalently or non-covalently. Proteins can be covalently immobilized using any method well known in the art, for example, but not limited to the method of Kadonaga and Tjian, 1986, Proc. Natl. Acad. Sci. USA 83:5889-5893, i.e., linkage to a cyanogen-bromide derivatized substrate such as CNBr-Sepharose 4B (Pharmacia). Where needed, the use of spacers can reduce steric hindrance by the substrate. Non- covalent attachment of proteins to a substrate include, but are not limited to, attachment of a protein to a charged surface, binding with specific antibodies, binding to a third unrelated interacting protein, etc.

Assays of agents (including cell extracts or a library pool) for competition for binding of one member of a complex (or derivatives thereof) with another member of the complex labeled by any means (e.g., those means described above) are provided to screen for competitors or enhancers of complex formation.

In specific embodiments, blocking agents to inhibit non-specific binding of reagents to other protein components, or absorptive losses of reagents to plastics, immobilization matrices, etc., are included in the assay mixture. Blocking agents include, but are not restricted to bovine serum albumin, β-casein, nonfat dried milk, Denhardt's reagent, Ficoll, polyvinylpyrolidine, nonionic detergents (NP40, Triton X-100, Tween 20, Tween 80, etc.), ionic detergents (e.g., SDS, LDS, etc.), polyethylene glycol, etc. Appropriate blocking agent concentrations allow complex formation.

After binding is performed, unbound, labeled protein is removed in the supernatant, and the immobilized protein retaining any bound, labeled protein is washed extensively. The amount of bound label is then quantified using standard methods in the art to detect the label as described, supra.

In another specific embodiments screening for modulators of the protein complexes/protein as provided herein can be carried out by attaching those and/or the antibodies as provided herein to a solid carrier. In a further specific embodiment, the invention relates to an array of said molecules.

The preparation of such an array containing different types of proteins, including antibodies) is well known in the art and is apparent to a person skilled in the art (see e.g. Ekins et al., 1989, J. Pharm. Biomed. Anal. 7:155-168; Mitchell et al. 2002, Nature Biotechnol. 20:225-229; Petricoin et al., 2002, Lancet 359:572-577; Templin et al., 2001 , Trends Biotechnol. 20:160-166; Wilson and Nock, 2001 , Curr. Opin. Chem. Biol. 6:81-85; Lee et al., 2002 Science 295:1702-1705; MacBeath and Schreiber, 2000, Science 289:1760; Blawas and Reichert, 1998, Biomaterials 19:595; Kane et al., 1999, Biomaterials 20:2363; Chen et al., 1997, Science 276:1425; Vaugham et al., 1996, Nature Biotechnol. 14:309-314; Mahler et al., 1997, Immunotechnology 3:31-43; Roberts et al., 1999, Curr. Opin. Chem. Biol. 3:268-273; Nord et al., 1997, Nature Biotechnol. 15:772-777; Nord et al., 2001 , Eur. J. Biochem. 268:4269-4277; Brody and Gold, 2000, Rev. Mol. Biotechnol. 74:5-13; Karlstroem and Nygren, 2001, Anal. Biochem. 295:22-30; Nelson et al., 2000, Electrophoresis 21:1155-1163; Honore et al., 2001 , Expert Rev. Mol. Diagn. 3:265-274; Albala, 2001 , Expert Rev. Mol. Diagn. 2:145-152, Figeys and Pinto, 2001, Electrophoresis 2:208-216 and references in the publications listed here).

Complexes can be attached to an array by different means as will be apparent to a person skilled in the art. Complexes can for example be added to the array via a TAP- tag (as described in WO/0009716 and in Rigaut et al., 1999, Nature Biotechnol. 10:1030- 1032) after the purification step or by another suitable purification scheme as will be apparent to a person skilled in the art.

Optionally, the proteins of the complex can be cross-linked to enhance the stability of the complex. Different methods to cross-link proteins are well known in the art. Reactive end-groups of cross-linking agents include but are not limited to -COOH, -SH, - NH2 or N-oxy-succinamate.

The spacer of the cross-linking agent should be chosen with respect to the size of the complex to be cross-linked. For small protein complexes, comprising only a few proteins, relatively short spacers are preferable in order to reduce the likelihood of cross-linking separate complexes in the reaction mixture. For larger protein complexes, additional use of larger spacers is preferable in order to facilitate cross-linking between proteins within the complex.

It is preferable to check the success-rate of cross-linking before linking the complex to the carrier.

As will be apparent to a person skilled in the art, the optimal rate of cross-linking need to be determined on a case by case basis. This can be achieved by methods well known in the art, some of which are exemplary described below.

A sufficient rate of cross-linking can be checked f.e. by analysing the cross-linked complex vs. a non-cross-linked complex on a denaturating protein gel. If cross-linking has been performed successfully, the proteins of the complex are expected to be found in the same lane, whereas the proteins of the non-cross-linked complex are expected to be separated according to their individual characteristics. Optionally the presence of all proteins of the complex can be further checked by peptide- sequencing of proteins in the respective bands using methods well known in the art such as mass spectrometry and/or Edman degradation.

In addition, a rate of crosslinking which is too high should also be avoided. If cross-linking has been carried out too extensively, there will be an increasing amount of cross-linking of the individual protein complex, which potentially interferes with a screening for potential binding partners and/or modulators etc. using the arrays. The presence of such structures can be determined by methods well known in the art and include e.g. gel-filtration experiments comparing the gel filtration profile solutions containing cross-linked complexes vs. uncross-linked complexes.

Optionally, functional assays as will be apparent to a person skilled in the art, some of which are exemplarily provided herein, can be performed to check the integrity of the complex.

Alternatively, members of the protein complex can be expressed as a single fusion protein and coupled to the matrix as will be apparent to a person skilled in the art.

Optionally, the attachment of the complex or proteins or antibody as outlined above can be further monitored by various methods apparent to a person skilled in the art. Those include, but are not limited to surface plasmon resonance (see e.g. McDonnel, 2001, Curr. Opin. Chem. Biol. 5:572-577; Lee, 2001, Trends Biotechnol. 19:217-222; Weinberger et al., 2000, 1 :395-416; Pearson et al., 2000, Ann. Clin. Biochem. 37:119- 145; Vely et al., 2000, Methods Mol. Biol. 121 :313-321 ; Slepak, 2000, J. Mol Recognit. 13:20-26.

Exemplary assays useful for measuring the Bcl-2 binding activity of the Bcl2-complex include but are not limited to those described in Hanada M et al., 1995, J Biol Chem, 270:11962-9.

Exemplary assays useful for measuring the cytochrome c release activity from mitochondria of the Bcl2-complex include but are not limited to those described in Bossy- Wetzel E and ., 2000, Methods Enzymol, 322:235-42.

Exemplary assays useful for measuring the apoptosis induction activity of the Bcl2- complex include but are not limited to those described in Bossy-Wetzel E and ., 2000, Methods Enzymol, 322:15-8.

Exemplary assays useful for measuring the Cell motility acitvity of the Gab1 signalling complex include but are not limited to those described in Petrelli Annalisa et al., 2002, Nature, 416:187-90.

Exemplary assays useful for measuring the Focus forming activity of the Gab1 signalling complex include but are not limited to those described in Giordano S et al., 1997, Proc Natl Acad Sci U S A, 94:13868-72.

Exemplary assays useful for measuring the Tumorigenicity and experimental metastatic activity of the Gab1 signalling complex include but are not limited to those described in Giordano S et al., 1997, Proc Natl Acad Sci U S A, 94:13868-72.

Exemplary assays useful for measuring the In vitro invasion activity of the Gab1 signalling complex include but are not limited to those described in Giordano S et al., 1997, Proc Natl Acad Sci U S A, 94:13868-72. Exemplary assays useful for measuring the Soft agar colony formation activity of the Gab1 signalling complex include but are not limited to those described in Giordano S et al., 1997, Proc Natl Acad Sci U S A, 94:13868-72.

Exemplary assays useful for measuring the Scatter activity of the Gab1 signalling complex include but are not limited to those described in Ponzetto C et al., 1996, J Biol Chem, 271 :14119-23.

Exemplary assays useful for measuring the kinase activity of the Her2 complex include but are not limited to those described in Engelman J A et al., 1998, J Biol Chem, 273:20448-55.

Exemplary assays useful for measuring the diacylglycerol kinase activity of the Her2 complex include but are not limited to those described in Walsh J P et al ., 1992, Methods Enzymol, 209:153-62.

Exemplary assays useful for measuring the sphingosine kinase activity of the Her2 complex include but are not limited to those described in Olivera A et al., 2000, Methods Enzymol, 311 :215-23.

Exemplary assays useful for measuring the kinase activation of the Ringo 1 complex include but are not limited to those described in Karaiskou A et al., 2001 , J Biol Chem, 276:36028-34.

Exemplary assays useful for measuring the DNA binding activity of the telomere capping complex include but are not limited to those described in Baumann P et al., 2001 , Science, 292:1171-5.

Exemplary assays useful for measuring the TRF2 binding activity of the telomere capping complex include but are not limited to those described in Song K et al., 2000, FEBS Lett, 481 :81-5. Exemplary assays useful for measuring the RAP1 binding activity of the telomere capping complex include but are not limited to those described in Li B et al., 2000, Cell, 101 :471-83.

4.6.1 CANDIDATE MOLECULES

Any molecule known in the art can be tested for its ability to modulate (increase or decrease) the amount of, activity of, or protein component composition of a complex of the present invention as detected by a change in the amount of, activity of, or protein component composition of, said complex. By way of example, a change in the amount of the complex can be detected by detecting a change in the amount of the complex that can be isolated from a cell expressing the complex machinery. For identifying a molecule that modulates complex activity, candidate molecules can be directly provided to a cell expressing the complex machinery, or, in the case of candidate proteins, can be provided by providing their encoding nucleic acids under conditions in which the nucleic acids are recombinantly expressed to produce the candidate proteins within the cell expressing the complex machinery, the complex is then isolated from the cell and the isolated complex is assayed for activity using methods well known in the art, not limited to those described, supra.

This embodiment of the invention is well suited to screen chemical libraries for molecules which modulate, e.g., inhibit, antagonize, or agonize, the amount of, activity of, or protein component composition of the complex. The chemical libraries can be peptide libraries, peptidomimetic libraries, chemically synthesized libraries, recombinant, e.g., phage display libraries, and in vitro translation-based libraries, other non-peptide synthetic organic libraries, etc.

Exemplary libraries are commercially available from several sources (ArQule, Tripos/PanLabs, ChemDesign, Pharmacopoeia). In some cases, these chemical libraries are generated using combinatorial strategies that encode the identity of each member of the library on a substrate to which the member compound is attached, thus allowing direct and immediate identification of a molecule that is an effective modulator. Thus, in many combinatorial approaches, the position on a plate of a compound specifies that compound's composition. Also, in one example, a single plate position may have from 1-20 chemicals that can be screened by administration to a well containing the interactions of interest. Thus, if modulation is detected, smaller and smaller pools of interacting pairs can be assayed for the modulation activity. By such methods, many candidate molecules can be screened.

Many diversity libraries suitable for use are known in the art and can be used to provide compounds to be tested according to the present invention. Alternatively, libraries can be constructed using standard methods. Chemical (synthetic) libraries, recombinant expression libraries, or polysome-based libraries are exemplary types of libraries that can be used.

The libraries can be constrained or semirigid (having some degree of structural rigidity), or linear or nonconstrained. The library can be a cDNA or genomic expression library, random peptide expression library or a chemically synthesized random peptide library, or non-peptide library. Expression libraries are introduced into the cells in which the assay occurs, where the nucleic acids of the library are expressed to produce their encoded proteins.

In one embodiment, peptide libraries that can be used in the present invention may be libraries that are chemically synthesized in vitro. Examples of such libraries are given in Houghten et al., 1991, Nature 354:84-86, which describes mixtures of free hexapeptides in which the first and second residues in each peptide were individually and specifically defined; Lam et al., 1991 , Nature 354:82-84, which describes a "one bead, one peptide" approach in which a solid phase split synthesis scheme produced a library of peptides in which each bead in the collection had immobilized thereon a single, random sequence of amino acid residues; Medynski, 1994, Bio/Technology 12:709-710, which describes split synthesis and T-bag synthesis methods; and Gallop et al., 1994, J. Med. Chem. 37:1233-1251. Simply by way of other examples, a combinatorial library may be prepared for use, according to the methods of Ohlmeyer et al., 1993, Proc. Natl. Acad. Sci. USA 90:10922-10926; Erb et al., 1994, Proc. Natl. Acad. Sci. USA 91:11422-11426; Houghten et al., 1992, Biotechniques 13:412; Jayawickreme et al., 1994, Proc. Natl. Acad. Sci. USA 91 :1614-1618; or Salmon et al., 1993, Proc. Natl. Acad. Sci. USA 90:11708-11712. PCT Publication No. WO 93/20242 and Brenner and Lerner, 1992, Proc. Natl. Acad. Sci. USA 89:5381-5383 describe "encoded combinatorial chemical libraries," that contain oligonucleotide identifiers for each chemical polymer library member. In a preferred embodiment, the library screened is a biological expression library that is a random peptide phage display library, where the random peptides are constrained (e.g., by virtue of having disulfide bonding).

Further, more general, structurally constrained, organic diversity (e.g., nonpeptide) libraries, can also be used. By way of example, a benzodiazepine library (see e.g., Bunin et al., 1994, Proc. Natl. Acad. Sci. USA 91:4708-4712) may be used.

Conformationally constrained libraries that can be used include but are not limited to those containing invariant cysteine residues which, in an oxidizing environment, crosslink by disulfide bonds to form cystines, modified peptides (e.g., incorporating fluorine, metals, isotopic labels, are phosphorylated, etc.), peptides containing one or more non-naturally occurring amino acids, non-peptide structures, and peptides containing a significant fraction of -carboxyglutamic acid.

Libraries of non-peptides, e.g., peptide derivatives (for example, that contain one or more non-naturally occurring amino acids) can also be used. One example of these are peptoid libraries (Simon et al., 1992, Proc. Natl. Acad. Sci. USA 89:9367-9371). Peptoids are polymers of non-natural amino acids that have naturally occurring side chains attached not to the α carbon but to the backbone amino nitrogen. Since peptoids are not easily degraded by human digestive enzymes, they are advantageously more easily adaptable to drug use. Another example of a library that can be used, in which the amide functionalities in peptides have been permethylated to generate a chemically transformed combinatorial library, is described by Ostresh et al., 1994, Proc. Natl. Acad. Sci. USA 91 :11138-11142).

The members of the peptide libraries that can be screened according to the invention are not limited to containing the 20 naturally occurring amino acids. In particular, chemically synthesized libraries and polysome based libraries allow the use of amino acids in addition to the 20 naturally occurring amino acids (by their inclusion in the precursor pool of amino acids used in library production). In specific embodiments, the library members contain one or more non-natural or non-classical amino acids or cyclic peptides. Non-classical amino acids include but are not limited to the D-isomers of the common amino acids, -amino isobutyric acid, 4-aminobutyric acid, Abu, 2-amino butyric acid;. -Abu,.-Ahx, 6-amino hexanoic acid; Aib, 2-amino isobutyric acid; 3-amino propionic acid; omithine; norleucine; norvaline, hydroxyproline, sarcosine, citrulline, cysteic acid, t- butylglycine, t-butylalanine, phenylglycine, cyclohexylalanine, β-alanine, designer amino acids such as β-methyl amino acids, C-methyl amino acids, N-methyl amino acids, fluoro-amino acids and amino acid analogs in general. Furthermore, the amino acid can be D (dextrorotary) or L (levorotary).

In a specific embodiment, fragments and/or analogs of complexes of the invention, or protein components thereof, especially peptidomimetics, are screened for activity as competitive or non-competitive inhibitors of complex activity or formation.

In another embodiment of the present invention, combinatorial chemistry can be used to identify modulators of a the complexes. Combinatorial chemistry is capable of creating libraries containing hundreds of thousands of compounds, many of which may be structurally similar. While high throughput screening programs are capable of screening these vast libraries for affinity for known targets, new approaches have been developed that achieve libraries of smaller dimension but which provide maximum chemical diversity. (See e.g., Matter, 1997, J. Med. Chem. 40:1219-1229).

One method of combinatorial chemistry, affinity fingerprinting, has previously been used to test a discrete library of small molecules for binding affinities for a defined panel of proteins. The fingerprints obtained by the screen are used to predict the affinity of the individual library members for other proteins or receptors of interest (in the instant invention, the protein complexes of the present invention and protein components thereof.) The fingerprints are compared with fingerprints obtained from other compounds known to react with the protein of interest to predict whether the library compound might similarly react. For example, rather than testing every ligand in a large library for interaction with a complex or protein component, only those ligands having a fingerprint similar to other compounds known to have that activity could be tested. (See, e.g., Kauvar et al., 1995, Chem. Biol. 2:107-118; Kauvar, 1995, Affinity fingerprinting, Pharmaceutical Manufacturing International. 8:25-28; and Kauvar, Toxic-Chemical Detection by Pattern Recognition in New Frontiers in Agrochemical Immunoassay, Kurtz, Stanker and Skerritt (eds), 1995, AOAC: Washington, D.C., 305-312).

Kay et al. (1993, Gene 128:59-65) disclosed a method of constructing peptide libraries that encode peptides of totally random sequence that are longer than those of any prior conventional libraries. The libraries disclosed in Kay et al. encode totally synthetic random peptides of greater than about 20 amino acids in length. Such libraries can be advantageously screened to identify complex modulators. (See also U.S. Patent No. 5,498,538 dated March 12, 1996; and PCT Publication No. WO 94/18318 dated August 18, 1994). A comprehensive review of various types of peptide libraries can be found in Gallop et al., 1994, J. Med. Chem. 37:1233-1251.

4.7 PHARMACEUTICAL COMPOSITIONS AND THERAPEUTIC/PROPHYLACTIC ADMINISTRATION

The invention provides methods of treatment (and prophylaxis) by administration to a subject of an effective amount of a therapeutic of the invention. In a preferred aspect, the therapeutic is substantially purified. The subject is preferably an animal including, but not limited to animals such as cows, pigs, horses, chickens, cats, dogs, etc., and is preferably a mammal, and most preferably human. In a specific embodiment, a non-human mammal is the subject.

Various delivery systems are known and can be used to administer a therapeutic of the invention, e.g., encapsulation in liposomes, microparticles, and microcapsules: use of recombinant cells capable of expressing the therapeutic, use of receptor-mediated endocytosis (e.g., Wu and Wu, 1987, J. Biol. Chem. 262:4429-4432); construction of a therapeutic nucleic acid as part of a retroviral or other vector, etc. Methods of introduction include but are not limited to intradermal, intramuscular, intraperitoneal, intravenous, subcutaneous, intranasal, epidural, and oral routes. The compounds may be administered by any convenient route, for example by infusion, by bolus injection, by absorption through epithelial or mucocutaneous linings (e.g., oral, rectal and intestinal mucosa, etc.), and may be administered together with other biologically active agents. Administration can be systemic or local. In addition, it may be desirable to introduce the pharmaceutical compositions of the invention into the central nervous system by any suitable route, including intraventricular and intrathecal injection; intraventricular injection may be facilitated by an intraventricular catheter, for example, attached to a reservoir, such as an Ommaya reservoir. Pulmonary administration can also be employed, e.g., by use of an inhaler or nebulizer, and formulation with an aerosolizing agent.

In a specific embodiment, it may be desirable to administer the pharmaceutical compositions of the invention locally to the area in need of treatment. This may be achieved by, for example, and not by way of limitation, local infusion during surgery, topical application, e.g., in conjunction with a wound dressing after surgery, by injection, by means of a catheter, by means of a suppository, or by means of an implant, said implant being of a porous, non-porous, or gelatinous material, including membranes, such as sialastic membranes, or fibers. In one embodiment, administration can be by direct injection at the site (or former site) of a malignant tumor or neoplastic or pre- neoplastic tissue.

In another embodiment, the therapeutic can be delivered in a vesicle, in particular a liposome (Langer, 1990, Science 249:1527-1533; Treat et al., 1989, In: Liposomes in the Therapy of Infectious Disease and Cancer, Lopez-Berestein and Fidler, eds., Liss, New York, pp. 353-365; Lopez-Berestein, ibid., pp. 317-327; see generally ibid.)

In yet another embodiment, the therapeutic can be delivered via a controlled release system. In one embodiment, a pump may be used (Langer, supra; Sefton, 1987, CRC Crit. Ref. Biomed. Eng. 14:201-240; Buchwald et al., 1980, Surgery 88:507-516; Saudek et al., 1989, N. Engl. J. Med. 321 :574-579). In another embodiment, polymeric materials can be used (Medical Applications of Controlled Release, Langer and Wise, eds., CRC Press, Boca Raton, Florida, 1974; Controlled Drug Bioavailability, Drug Product Design and Performance, Smolen and Ball, eds., Wiley, New York, 1984; Ranger and Peppas, 1983, Macromol. Sci. Rev. Macromol. Chem. 23:61 ; Levy et al., 1985, Science 228:190-192; During et al., 1989, Ann. Neurol. 25:351-356; Howard et al., 1989, J. Neurosurg. 71:858-863). In yet another embodiment, a controlled release system can be placed in proximity of the therapeutic target, i.e., the brain, thus requiring only a fraction of the systemic dose (e.g., Goodson, 1984, In: Medical Applications of Controlled Release, supra, Vol. 2, pp. 115-138). Other controlled release systems are discussed in the review by Langer (1990, Science 249:1527-1533).

In a specific embodiment where the therapeutic is a nucleic acid encoding a protein therapeutic, the nucleic acid can be administered in vivo to promote expression of its encoded protein, by constructing it as part of an appropriate nucleic acid expression vector and administering it so that it becomes intracellular, e.g., by use of a retroviral vector (U.S. Patent No. 4,980,286), or by direct injection, or by use of microparticle bombardment (e.g., a gene gun; Biolistic, Dupont), or by coating it with lipids, cell-surface receptors or transfecting agents, or by administering it in linkage to a homeobox-like peptide which is known to enter the nucleus (e.g., Joliot et al., 1991 , Proc. Natl. Acad. Sci. USA 88:1864-1868), etc. Alternatively, a nucleic acid therapeutic can be introduced intracellularly and incorporated by homologous recombination within host cell DNA for expression. The present invention also provides pharmaceutical compositions. Such compositions comprise a therapeutically effective amount of a therapeutic, and a pharmaceutically acceptable carrier. In a specific embodiment, the term "pharmaceutically acceptable" means approved by a regulatory agency of the Federal or a state government or listed in the U.S. Pharmacopeia or other generally recognized pharmacopeia for use in animals, and more particularly, in humans. The term "carrier" refers to a diluent, adjuvant, excipient, or vehicle with which the therapeutic is administered. Such pharmaceutical carriers can be sterile liquids, such as water and oils, including those of petroleum, animal, vegetable or synthetic origin, including but not limited to peanut oil, soybean oil, mineral oil, sesame oil and the like. Water is a preferred carrier when the pharmaceutical composition is administered orally. Saline and aqueous dextrose are preferred carriers when the pharmaceutical composition is administered intravenously. Saline solutions and aqueous dextrose and glycerol solutions are preferably employed as liquid carriers for injectable solutions. Suitable pharmaceutical excipients include starch, glucose, lactose, sucrose, gelatin, malt, rice, flour, chalk, silica gel, sodium stearate, glycerol monostearate, talc, sodium chloride, dried skim milk, glycerol, propylene, glycol, water, ethanol and the like. The composition, if desired, can also contain minor amounts of wetting or emulsifying agents, or pH buffering agents. These compositions can take the form of solutions, suspensions, emulsions, tablets, pills, capsules, powders, sustained-release formulations and the like. The composition can be formulated as a suppository, with traditional binders and carriers such as triglycerides. Oral formulation can include standard carriers such as pharmaceutical grades of mannitol, lactose, starch, magnesium stearate, sodium saccharine, cellulose, magnesium carbonate, etc. Examples of suitable pharmaceutical carriers are described in "Remington's Pharmaceutical Sciences" by E.W. Martin. Such compositions will contain a therapeutically effective amount of the therapeutic, preferably in purified form, together with a suitable amount of carrier so as to provide the form for proper administration to the patient. The formulation should suit the mode of administration.

In a preferred embodiment, the composition is formulated, in accordance with routine procedures, as a pharmaceutical composition adapted for intravenous administration to human beings. Typically, compositions for intravenous administration are solutions in sterile isotonic aqueous buffer. Where necessary, the composition may also include a solubilizing agent and a local anesthetic such as lidocaine to ease pain at the site of the injection. Generally, the ingredients are supplied either separately or mixed together in unit dosage form, for example, as a dry lyophilized powder or water- free concentrate in a hermetically sealed container such as an ampoule or sachette indicating the quantity of active agent. Where the composition is to be administered by infusion, it can be dispensed with an infusion bottle containing sterile pharmaceutical grade water or saline. Where the composition is administered by injection, an ampoule of sterile water or saline for injection can be provided so that the ingredients may be mixed prior to administration.

The therapeutics of the invention can be formulated as neutral or salt forms. Pharmaceutically acceptable salts include those formed with free carboxyl groups such as those derived from hydrochloric, phosphoric, acetic, oxalic, tartaric acids, etc., those formed with free amine groups such as those derived from isopropylamine, triethylamine, 2-ethylamino ethanol, histidine, procaine, etc., and those derived from sodium, potassium, ammonium, calcium, and ferric hydroxides, etc.

The amount of the therapeutic of the invention which will be effective in the treatment of a particular disorder or condition will depend on the nature of the disorder or condition, and can be determined by standard clinical techniques. In addition, in vitro assays may optionally be employed to help identify optimal dosage ranges. The precise dose to be employed in the formulation will also depend on the route of administration, and the seriousness of the disease or disorder, and should be decided according to the judgment of the practitioner and each patient's circumstances. However, suitable dosage ranges for intravenous administration are generally about 20-500 micrograms of active compound per kilogram body weight. Suitable dosage ranges for intranasal administration are generally about 0.01 pg/kg body weight to 1 mg/kg body weight. Effective doses may be extrapolated from dose-response curves derived from in vitro or animal model test systems.

Suppositories generally contain active ingredient in the range of 0.5% to 10% by weight; oral formulations preferably contain 10% to 95% active ingredient.

The invention also provides a pharmaceutical pack or kit comprising one or more containers filled with one or more of the ingredients of the pharmaceutical compositions of the invention. Optionally associated with such container(s) can be a notice in the form prescribed by a governmental agency regulating the manufacture, use or sale of pharmaceuticals or biological products, which notice reflects approval by the agency of manufacture, use or sale for human administration. The invention also provides a pharmaceutical pack or kit comprising one or more containers filled with one or more of the ingredients of the pharmaceutical compositions of the invention. For example, the kit can comprise in one or more containers a first protein, or a functionally active fragment or functionally active derivative thereof, which first protein is selected from the group consisting of proteins listed in the fourth column of table 1 ; and a second protein, or a functionally active fragment or functionally active derivative thereof, which second protein is selected from the group consisting of proteins listed in the fifth column of table 1.

Alternatively, the kit can comprise in one or more containers, all proteins, functionally active fragments or functionally active derivatives thereof of from the group of proteins in the sixth column of table 1.

The kits of the present invention can also contain expression vectors encoding the essential components of the complex machinery, which components after being expressed can be reconstituted in order to form a biologically active complex. Such a kit preferably also contains the required buffers and reagents. Optionally associated with such container(s) can be instructions for use of the kit and/or a notice in the form prescribed by a governmental agency regulating the manufacture, use or sale of pharmaceuticals or biological products, which notice reflects approval by the agency of manufacture, use or sale for human administration.

4.8 ANIMAL MODELS

The present invention also provides animal models. In one embodiment, animal models for diseases and disorders involving the protein complexes of the present invention are provided. These animal models are well known in the art. These animal models include, but are not limited to those which are listed in the section 4.6 (supra) as exemplary animald models to study any of the complexes provided in the invention. Such animals can be initially produced by promoting homologous recombination or insertional mutagenesis between genes encoding the protein components of the complexes in the chromosome, and exogenous genes encoding the protein components of the complexes that have been rendered biologically inactive or deleted (preferably by insertion of a heterologous sequence, e.g., an antibiotic resistance gene). In a preferred aspect, homologous recombination is carried out by transforming embryo-derived stem (ES) cells with one or more vectors containing one or more insertionally inactivated genes, such that homologous recombination occurs, followed by injecting the transformed ES cells into a blastocyst, and implanting the blastocyst into a foster mother, followed by the birth of the chimeric animal ("knockout animal") in which a gene encoding a component protein from the fourth column of table 1 , or a functionally active fragment or functionally active derivative thereof, and a gene encoding a component protein from the fifth column of table 1 , or a functionally active fragment or functionally active derivative thereof, has been inactivated or deleted (Capecchi, 1989, Science 244:1288-1292). In another preferred aspect, homologous recombination is carried out by transforming embryo-derived stem (ES) cells with one or more vectors containing one or more insertionally inactivated genes, such that homologous recombination occurs, followed by injecting the transformed ES cells into a blastocyst, and implanting the blastocyst into a foster mother, followed by the birth of the chimeric animal ("knockout animal") in which the genes of all component proteins from the group of proteins listed in the fourth column of table 1 or of all proteins from the group of proteins listed in the fifth column of table 1 have been inactivated or deleted.

The chimeric animal can be bred to produce additional knockout animals. Such animals can be mice, hamsters, sheep, pigs, cattle, etc., and are preferably non-human mammals. In a specific embodiment, a knockout mouse is produced.

Such knockout animals are expected to develop, or be predisposed to developing, diseases or disorders associated with mutations involving the protein complexes of the present invention, and thus, can have use as animal models of such diseases and disorders, e.g., to screen for or test molecules (e.g., potential therapeutics) for such diseases and disorders.

In a different embodiment of the invention, transgenic animals that have incorporated and express (or over-express or mis-express) a functional gene encoding a protein component of the complex, e.g. by introducing the a gene encoding one or more of the components of the complex under the control of a heterologous promoter (i.e., a promoter that is not the native promoter of the gene) that either over-expresses the protein or proteins, or expresses them in tissues not normally expressing the complexes or proteins, can have use as animal models of diseases and disorders characterized by elevated levels of the protein complexes. Such animals can be used to screen or test molecules for the ability to treat or prevent the diseases and disorders cited supra. In one embodiment, the present invention provides a recombinant non-human animal in which an endogenous gene encoding a first protein, or a functionally active fragment or functionally active derivative thereof, which first protein is selected from the group of proteins listed in the fourth column of table 1 , and and endogenous gene encoding a second protein, or a functionally active fragment or functionally active derivative thereof, which second protein is selected from the group consisting of proteins listed in the fifth column of table 1 has been deleted or inactivated by homologous recombination or insertional mutagenesis of said animal or an ancestor thereof. In addition, the present invention provides a recombinant non-human animal in which the endogenous genes of all proteins, or functionally active fragments or functionally active derivatives thereof of one of the group of proteins listed in the sixth column have been deleted or inactivated by homologous recombination or insertional mutagenesis of said animal or an ancestor thereof:

In another embodiment, the present invention provides a recombinant non-human animal in which an endogenous gene encoding a first protein, or a functionally active fragment or functionally active derivative thereof, which first protein is selected from the group consisting of proteins of the fourth column of table 1 , and endogenous gene encoding a second protein, or a functionally active fragment or functionally active derivative thereof, which second protein is selected from the group consisting of proteins of the fifth column, of table 1 are recombinantly expressed in said animal or an ancestor thereof.

The following series of examples are presented by way of illustration and not by way of limitation on the scope of the invention.

EXAMPLES

An object of the present invention was to identify protein complexes of the APP processing pathway, component proteins of the said complexes, fragments and derivatives of the component proteins, and antibodies specific to the complexes. The present invention also relates to methods for use of the complexes of the APP processing pathway and their interacting proteins in, inter alia, screening, diagnosis, and therapy, as well as to methods of preparing the complexes. By applying the process according to the invention said complexes were identified. The components are listed in table 1.

Those complexes are, as called herein, the following complexes:

Telomere capping protein complex, Her2-protein complex, Ringol -protein complex, Bcl2-protein complex, Gab1 -signalling protein complex.

Thus the invention relates to the following embodiments of the Telomere Capping Protein Complex

1. A protein complex selected from complex (I) and comprising

(a) at least one first protein selected from the group consisting of:

(i) "Pot1 " (SEQ ID No:38) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Pot1" encoded by a nucleic acid that hybridizes to the "Pot1 " nucleic acid or its complement under low stringency conditions, and

(b) at least one second protein, which second protein is selected from the group consisting of:

(i) "38 KDA FK-506 BINDING PROTEIN HOMOLOG" (SEQ ID No:1) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "38 KDA FK-506 BINDING PROTEIN HOMOLOG" encoded by a nucleic acid that hybridizes to the "38 KDA FK-506 BINDING PROTEIN HOMOLOG" nucleic acid or its complement under low stringency conditions,

(ii) "ANTIGEN NY-CO-7" (SEQ ID No:2) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ANTIGEN NY- CO-7" encoded by a nucleic acid that hybridizes to the "ANTIGEN NY-CO-7" nucleic acid or its complement under low stringency conditions,

(iii) "ATP-BINDING CASSETTE, SUB-FAMILY D, MEMBER 3" (SEQ ID No:3) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ATP-BINDING CASSETTE, SUB-FAMILY D, MEMBER 3" encoded by a nucleic acid that hybridizes to the "ATP-BINDING CASSETTE, SUBFAMILY D, MEMBER 3" nucleic acid or its complement under low stringency conditions, (iv) "ATP-DEPENDENT DNA HELICASE II, 80 KDA SUBUNIT" (SEQ ID No:4) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ATP-DEPENDENT DNA HELICASE II, 80 KDA SUBUNIT" encoded by a nucleic acid that hybridizes to the "ATP-DEPENDENT DNA

HELICASE II, 80 KDA SUBUNIT" nucleic acid or its complement under low stringency conditions,

(v) "BAF180" (SEQ ID No:5) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "BAF180" encoded by a nucleic acid that hybridizes to the "BAF180" nucleic acid or its complement under low stringency conditions,

(vi) "CASEIN KINASE II, ALPHA CHAIN" (SEQ ID No:6) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CASEIN KINASE II, ALPHA CHAIN" encoded by a nucleic acid that hybridizes to the "CASEIN KINASE II, ALPHA CHAIN" nucleic acid or its complement under low stringency conditions,

(vii) "CDNA FLJ13664 FIS, CLONE PLACE1011649" (SEQ ID No:7) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ13664 FIS, CLONE PLACE1011649" encoded by a nucleic acid that hybridizes to the "CDNA FLJ 13664 FIS, CLONE PLACE1011649" nucleic acid or its complement under low stringency conditions,

(viii) "CDNA FLJ13998 FIS, CLONE Y79AA1002229" (SEQ ID No:8) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ13998 FIS, CLONE Y79AA1002229" encoded by a nucleic acid that hybridizes to the "CDNA FLJ13998 FIS, CLONE Y79AA1002229" nucleic acid or its complement under low stringency conditions,

(ix) "CDNA FLJ20643 FIS, CLONE KAT02633" (SEQ ID No:9) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ20643 FIS, CLONE KAT02633" encoded by a nucleic acid that hybridizes to the "CDNA FLJ20643 FIS, CLONE KAT02633" nucleic acid or its complement under low stringency conditions,

(x) "CDNA FLJ25320 FIS, CLONE TST00267 (FRAGMENT)" (SEQ ID No:10) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ25320 FIS, CLONE TST00267

(FRAGMENT)" encoded by a nucleic acid that hybridizes to the "CDNA FLJ25320 FIS,

CLONE TST00267 (FRAGMENT)" nucleic acid or its complement under low stringency conditions, (xi) "CDNA FLJ31741 FIS, CLONE NT2RI2007148" (SEQ ID No:11) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ31741 FIS, CLONE NT2RI2007148" encoded by a nucleic acid that hybridizes to the "CDNA FLJ31741 FIS, CLONE NT2R12007148" nucleic acid or its complement under low stringency conditions,

(xii) "CDNA: FLJ21908 FIS, CLONE HEP03830" (SEQ ID No:12) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA: FLJ21908 FIS, CLONE HEP03830" encoded by a nucleic acid that hybridizes to the "CDNA: FLJ21908 FIS, CLONE HEP03830" nucleic acid or its complement under low stringency conditions,

(xiii) "CENP-F KINETOCHORE PROTEIN" (SEQ ID No:13) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CENP-F KINETOCHORE PROTEIN" encoded by a nucleic acid that hybridizes to the "CENP-F KINETOCHORE PROTEIN" nucleic acid or its complement under low stringency conditions,

(xiv) "CHROMATIN ASSEMBLY FACTOR 1 SUBUNIT C" (SEQ ID No:14) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CHROMATIN ASSEMBLY FACTOR 1 SUBUNIT C" encoded by a nucleic acid that hybridizes to the "CHROMATIN ASSEMBLY FACTOR 1

SUBUNIT C" nucleic acid or its complement under low stringency conditions,

(xv) "DNA MISMATCH REPAIR PROTEIN MSH6" (SEQ ID No:15) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "DNA MISMATCH REPAIR PROTEIN MSH6" encoded by a nucleic acid that hybridizes to the "DNA MISMATCH REPAIR PROTEIN MSH6" nucleic acid or its complement under low stringency conditions,

(xvi) "DNA-DEPENDENT PROTEIN KINASE CATALYTIC SUBUNIT" (SEQ ID No:16) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "DNA-DEPENDENT PROTEIN KINASE CATALYTIC

SUBUNIT" encoded by a nucleic acid that hybridizes to the "DNA-DEPENDENT

PROTEIN KINASE CATALYTIC SUBUNIT" nucleic acid or its complement under low stringency conditions,

(xvii) "DNA-DIRECTED RNA POLYMERASE II 23 KDA POLYPEPTIDE" (SEQ ID No:17) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "DNA-DIRECTED RNA POLYMERASE II 23 KDA POLYPEPTIDE" encoded by a nucleic acid that hybridizes to the "DNA-DIRECTED RNA POLYMERASE II 23 KDA POLYPEPTIDE" nucleic acid or its complement under low stringency conditions,

(xviii) "ELONGATION FACTOR 2 KINASE" (SEQ ID No: 18) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ELONGATION FACTOR 2 KINASE" encoded by a nucleic acid that hybridizes to the "ELONGATION FACTOR 2 KINASE" nucleic acid or its complement under low stringency conditions,

(xix) "FK506-BINDING PROTEIN 4" (SEQ ID No:19) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "FK506-BINDING PROTEIN 4" encoded by a nucleic acid that hybridizes to the "FK506- BINDING PROTEIN 4" nucleic acid or its complement under low stringency conditions, (xx) "GLIAL FIBRILLARY ACIDIC PROTEIN, ASTROCYTE" (SEQ ID No:20) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "GLIAL FIBRILLARY ACIDIC PROTEIN, ASTROCYTE" encoded by a nucleic acid that hybridizes to the "GLIAL FIBRILLARY ACIDIC PROTEIN, ASTROCYTE" nucleic acid or its complement under low stringency conditions, (xxi) "HDCMD34P" (SEQ ID No:21) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HDCMD34P" encoded by a nucleic acid that hybridizes to the "HDCMD34P" nucleic acid or its complement under low stringency conditions,

(xxii) "HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN H'" (SEQ ID No:22) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN H'" encoded by a nucleic acid that hybridizes to the "HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN H'" nucleic acid or its complement under low stringency conditions,

(xxiii) "HISTONE ACETYLTRANSFERASE TYPE B SUBUNIT 2" (SEQ ID No:23) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HISTONE ACETYLTRANSFERASE TYPE B SUBUNIT 2" encoded by a nucleic acid that hybridizes to the "HISTONE ACETYLTRANSFERASE TYPE B SUBUNIT 2" nucleic acid or its complement under low stringency conditions, (xxiv) "HSPC029" (SEQ ID No:24) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HSPC029" encoded by a nucleic acid that hybridizes to the "HSPC029" nucleic acid or its complement under low stringency conditions,

(xxv) "HYPOTHETICAL PROTEIN K1AA0310 (FRAGMENT)" (SEQ ID No:25) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYPOTHETICAL PROTEIN KIAA0310 (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "HYPOTHETICAL PROTEIN KIAA0310

(FRAGMENT)" nucleic acid or its complement under low stringency conditions,

(xxvi) "INCOMPATIBILITY PROTEIN HET-E-1 (FRAGMENT)" (SEQ ID No:26) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "INCOMPATIBILITY PROTEIN HET-E-1 (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "INCOMPATIBILITY PROTEIN HET-E-1

(FRAGMENT)" nucleic acid or its complement under low stringency conditions,

(xxvii) "KIAA0792 PROTEIN" (SEQ ID No:27) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA0792

PROTEIN" encoded by a nucleic acid that hybridizes to the "KIAA0792 PROTEIN" nucleic acid or its complement under low stringency conditions,

(xxviii) "KIAA1284 PROTEIN (FRAGMENT)" (SEQ ID No:28) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA1284 PROTEIN (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "KIAA1284 PROTEIN (FRAGMENT)" nucleic acid or its complement under low stringency conditions,

(xxix) "MEPRIN A BETA-SUBUNIT PRECURSOR" (SEQ ID No:29) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "MEPRIN A BETA-SUBUNIT PRECURSOR" encoded by a nucleic acid that hybridizes to the "MEPRIN A BETA-SUBUNIT PRECURSOR" nucleic acid or its complement under low stringency conditions,

(xxx) "MUTS" (SEQ ID No:30) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "MUTS" encoded by a nucleic acid that hybridizes to the "MUTS" nucleic acid or its complement under low stringency conditions,

(xxxi) "MYELOID LEUKEMIA FACTOR 2" (SEQ ID No:31) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "MYELOID LEUKEMIA FACTOR 2" encoded by a nucleic acid that hybridizes to the "MYELOID LEUKEMIA FACTOR 2" nucleic acid or its complement under low stringency conditions,

(xxxii) "NEIGHBOR OF A-KINASE ANCHORING PROTEIN 95" (SEQ ID No:32) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "NEIGHBOR OF A-KINASE ANCHORING PROTEIN 95" encoded by a nucleic acid that hybridizes to the "NEIGHBOR OF A-KINASE ANCHORING PROTEIN 95" nucleic acid or its complement under low stringency conditions,

(xxxiii) "P30 DBC" (SEQ ID No:33) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "P30 DBC" encoded by a nucleic acid that hybridizes to the "P30 DBC" nucleic acid or its complement under low stringency conditions,

(xxxiv) "PROBABLE UBIQUITIN CARBOXYL-TERMINAL HYDROLASE FAF-X" (SEQ ID No:34) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PROBABLE UBIQUITIN CARBOXYL- TERMINAL HYDROLASE FAF-X" encoded by a nucleic acid that hybridizes to the "PROBABLE UBIQUITIN CARBOXYL-TERMINAL HYDROLASE FAF-X" nucleic acid or its complement under low stringency conditions,

(xxxv) "PROGRAMED CELL DEATH PROTEIN 2" (SEQ ID No:35) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PROGRAMED CELL DEATH PROTEIN 2" encoded by a nucleic acid that hybridizes to the "PROGRAMED CELL DEATH PROTEIN 2" nucleic acid or its complement under low stringency conditions,

(xxxvi) "PROLIFERATING CELL NUCLEAR ANTIGEN" (SEQ ID No:36) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PROLIFERATING CELL NUCLEAR ANTIGEN" encoded by a nucleic acid that hybridizes to the "PROLIFERATING CELL NUCLEAR ANTIGEN" nucleic acid or its complement under low stringency conditions,

(xxxvii) "PROTEASOME SUBUNIT BETA TYPE 3" (SEQ ID No:37) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PROTEASOME SUBUNIT BETA TYPE 3" encoded by a nucleic acid that hybridizes to the "PROTEASOME SUBUNIT BETA TYPE 3" nucleic acid or its complement under low stringency conditions, (xxxviii) "RAD50 HOMOLOGUE HSRAD50" (SEQ ID No:39) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "RAD50 HOMOLOGUE HSRAD50" encoded by a nucleic acid that hybridizes to the "RAD50 HOMOLOGUE HSRAD50" nucleic acid or its complement under low stringency conditions,

(xxxix) "RAS GTPASE-ACTIVATING-LIKE PROTEIN IQGAP2" (SEQ ID No:40) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "RAS GTPASE-ACTIVATING-LIKE PROTEIN IQGAP2" encoded by a nucleic acid that hybridizes to the "RAS GTPASE-ACTIVATING-LIKE PROTEIN IQGAP2" nucleic acid or its complement under low stringency conditions, (xl) "SERINE/THREONINE PROTEIN PHOSPHATASE PP1 -ALPHA 1 CATALYTIC SUBUNIT" (SEQ ID No:41) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SERINE/THREONINE PROTEIN PHOSPHATASE PP1 -ALPHA 1 CATALYTIC SUBUNIT" encoded by a nucleic acid that hybridizes to the "SERINE/THREONINE PROTEIN PHOSPHATASE PP1- ALPHA 1 CATALYTIC SUBUNIT" nucleic acid or its complement under low stringency conditions,

(xli) "SERINE/THREONINE PROTEIN PHOSPHATASE PP1-BETA CATALYTIC SUBUNIT" (SEQ ID No:42) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SERINE/THREONINE PROTEIN PHOSPHATASE PP1-BETA CATALYTIC SUBUNIT" encoded by a nucleic acid that hybridizes to the "SERINE/THREONINE PROTEIN PHOSPHATASE PP1- BETA CATALYTIC SUBUNIT" nucleic acid or its complement under low stringency conditions,

(xlii) "SERINE/THREONINE PROTEIN PHOSPHATASE PP1 -GAMMA CATALYTIC SUBUNIT" (SEQ ID No:43) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SERINE/THREONINE PROTEIN PHOSPHATASE PP1 -GAMMA CATALYTIC SUBUNIT" encoded by a nucleic acid that hybridizes to the "SERINE/THREONINE PROTEIN PHOSPHATASE PP1- GAMMA CATALYTIC SUBUNIT" nucleic acid or its complement under low stringency conditions,

(xliii) "SIMILAR TO OROSOMUCOID 1 " (SEQ ID No:44) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SIMILAR TO OROSOMUCOID 1" encoded by a nucleic acid that hybridizes to the "SIMILAR TO OROSOMUCOID 1 " nucleic acid or its complement under low stringency conditions,

(xliv) "SMC5 PROTEIN" (SEQ ID No:45) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SMC5

PROTEIN" encoded by a nucleic acid that hybridizes to the "SMC5 PROTEIN" nucleic acid or its complement under low stringency conditions,

(xlv) "SQUAMOUS CELL CARCINOMA ANTIGEN 1 " (SEQ ID No:46) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SQUAMOUS CELL CARCINOMA ANTIGEN 1 " encoded by a nucleic acid that hybridizes to the "SQUAMOUS CELL CARCINOMA ANTIGEN 1 " nucleic acid or its complement under low stringency conditions,

(xlvi) "SUPPRESSOR OF G2 ALLELE OF SKP1 HOMOLOG" (SEQ ID No:47) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SUPPRESSOR OF G2 ALLELE OF SKP1 HOMOLOG" encoded by a nucleic acid that hybridizes to the "SUPPRESSOR OF G2 ALLELE OF

SKP1 HOMOLOG" nucleic acid or its complement under low stringency conditions,

(xlvii) "Serine/threonine proteine phosphatase 2A, catalytic subunit, beta isoform" (SEQ

ID No:48) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Serine/threonine proteine phosphatase 2A, catalytic subunit, beta isoform" encoded by a nucleic acid that hybridizes to the

"Serine/threonine proteine phosphatase 2A, catalytic subunit, beta isoform" nucleic acid or its complement under low stringency conditions,

(xlviii) "Similar to diacylglycerol kinase delta" (SEQ ID No:49) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Similar to diacylglycerol kinase delta" encoded by a nucleic acid that hybridizes to the "Similar to diacylglycerol kinase delta" nucleic acid or its complement under low stringency conditions,

(xlix) "TELOMERASE-BINDING PROTEIN P23" (SEQ ID No:50) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TELOMERASE-BINDING PROTEIN P23" encoded by a nucleic acid that hybridizes to the "TELOMERASE-BINDING PROTEIN P23" nucleic acid or its complement under low stringency conditions,

(I) "TELOMERIC REPEAT BINDING FACTOR 2" (SEQ ID No:51) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TELOMERIC REPEAT BINDING FACTOR 2" encoded by a nucleic acid that hybridizes to the "TELOMERIC REPEAT BINDING FACTOR 2" nucleic acid or its complement under low stringency conditions,

(Ii) "TERF1 (TRFI)-INTERACTING NUCLEAR FACTOR 2" (SEQ ID No:52) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TERF1 (TRFI)-INTERACTING NUCLEAR FACTOR 2" encoded by a nucleic acid that hybridizes to the "TERF1 (TRFI)-INTERACTING NUCLEAR FACTOR 2" nucleic acid or its complement under low stringency conditions, (Iii) "TRF1 " (SEQ ID No:53) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TRF1 " encoded by a nucleic acid that hybridizes to the "TRF1 " nucleic acid or its complement under low stringency conditions,

(liii) "TRF2-INTERACTING TELOMERIC RAP1 PROTEIN" (SEQ ID No:54) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TRF2-INTERACTING TELOMERIC RAP1 PROTEIN" encoded by a nucleic acid that hybridizes to the "TRF2-INTERACTING TELOMERIC RAP1 PROTEIN" nucleic acid or its complement under low stringency conditions, (liv) "TRICARBOXYLATE TRANSPORT PROTEIN, MITOCHONDRIAL PRECURSOR" (SEQ ID No:55) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TRICARBOXYLATE TRANSPORT PROTEIN, MITOCHONDRIAL PRECURSOR" encoded by a nucleic acid that hybridizes to the "TRICARBOXYLATE TRANSPORT PROTEIN, MITOCHONDRIAL PRECURSOR" nucleic acid or its complement under low stringency conditions, (Iv) "U5 SMALL NUCLEAR RIBONUCLEOPROTEIN 200 KDA HELICASE (FRAGMENT)" (SEQ ID No:56) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "U5 SMALL NUCLEAR RIBONUCLEOPROTEIN 200 KDA HELICASE (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "U5 SMALL NUCLEAR RIBONUCLEOPROTEIN 200 KDA HELICASE (FRAGMENT)" nucleic acid or its complement under low stringency conditions, and

(Ivi) "WD-REPEAT PROTEIN AN11 HOMOLOG" (SEQ ID No:57) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "WD-REPEAT PROTEIN AN11 HOMOLOG" encoded by a nucleic acid that hybridizes to the "WD-REPEAT PROTEIN AN11 HOMOLOG" nucleic acid or its complement under low stringency conditions, and a complex (II) comprising at least two of said second proteins, wherein said low stringency conditions comprise hybridization in a buffer comprising 35% formamide, 5X SSC, 50 mM Tris-HCI (pH 7.5), 5 mM EDTA, 0.02% PVP, 0.02% Ficoll, 0.2% BSA, 100 ug/ml denatured salmon sperm DNA, and 10% (wt/vol) dextran sulfate for 18-20 hours at 40 Celsius, washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4), 5 mM EDTA, and 0.1 % SDS for 1.5 hours at 55 Celsius, and washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4), 5 mM EDTA, and 0.1% SDS for 1.5 hours at 60 Celsius.

2. The protein complex according to No. 1 wherein the first protein is the protein Pot1 (SEQ ID NO. 38), or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of 'Pot1 ' encoded by a nucleic acid that hybridizes to the 'Pot1' under low stringency conditions.

3. The protein complex according to No. 1 selected from complex (I) and comprising the following proteins:

(iii) "ATP-BINDING CASSETTE, SUB-FAMILY D, MEMBER 3" (SEQ ID No:3) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ATP-BINDING CASSETTE, SUB-FAMILY D, MEMBER 3" encoded by a nucleic acid that hybridizes to the "ATP-BINDING CASSETTE, SUBFAMILY D, MEMBER 3" nucleic acid or its complement under low stringency conditions, (iv) "ATP-DEPENDENT DNA HELICASE II, 80 KDA SUBUNIT" (SEQ ID No:4) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ATP-DEPENDENT DNA HELICASE II, 80 KDA SUBUNIT" encoded by a nucleic acid that hybridizes to the "ATP-DEPENDENT DNA HELICASE II, 80 KDA SUBUNIT" nucleic acid or its complement under low stringency conditions,

(vii) "CDNA FLJ13664 FIS, CLONE PLACE1011649" (SEQ ID No:7) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ13664 FIS, CLONE PLACE1011649" encoded by a nucleic acid that hybridizes to the "CDNA FLJ13664 FIS, CLONE PLACE1011649" nucleic acid or its complement under low stringency conditions,

(viii) "CDNA FLJ13998 FIS, CLONE Y79AA1002229" (SEQ ID No:8) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ 13998 FIS, CLONE Y79AA1002229" encoded by a nucleic acid that hybridizes to the "CDNA FLJ13998 FIS, CLONE Y79AA1002229" nucleic acid or its complement under low stringency conditions,

CLONE TST00267 (FRAGMENT)" nucleic acid or its complement under low stringency conditions,

(xi) "CDNA FLJ31741 FIS, CLONE NT2RI2007148" (SEQ ID No:11) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ31741 FIS, CLONE NT2RI2007148" encoded by a nucleic acid that hybridizes to the "CDNA FLJ31741 FIS, CLONE NT2RI2007148" nucleic acid or its complement under low stringency conditions,

(xiii) "CENP-F KINETOCHORE PROTEIN" (SEQ ID No: 13) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CENP-F KINETOCHORE PROTEIN" encoded by a nucleic acid that hybridizes to the "CENP-F KINETOCHORE PROTEIN" nucleic acid or its complement under low stringency conditions,

SUBUNIT C" nucleic acid or its complement under low stringency conditions,

SUBUNIT" encoded by a nucleic acid that hybridizes to the "DNA-DEPENDENT

(xvii) "DNA-DIRECTED RNA POLYMERASE II 23 KDA POLYPEPTIDE" (SEQ ID No:17) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "DNA-DIRECTED RNA POLYMERASE II 23 KDA

POLYPEPTIDE" encoded by a nucleic acid that hybridizes to the "DNA-DIRECTED RNA POLYMERASE II 23 KDA POLYPEPTIDE" nucleic acid or its complement under low stringency conditions,

(xviii) "ELONGATION FACTOR 2 KINASE" (SEQ ID No:18) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ELONGATION FACTOR 2 KINASE" encoded by a nucleic acid that hybridizes to the "ELONGATION FACTOR 2 KINASE" nucleic acid or its complement under low stringency conditions,

(xxii) "HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN H'" (SEQ ID No:22) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN H'" encoded by a nucleic acid that hybridizes to the "HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN H"' nucleic acid or its complement under low stringency conditions,

(xxv) "HYPOTHETICAL PROTEIN KIAA0310 (FRAGMENT)" (SEQ ID No:25) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYPOTHETICAL PROTEIN KIAA0310 (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "HYPOTHETICAL PROTEIN KIAA0310

(FRAGMENT)" nucleic acid or its complement under low stringency conditions,

(xxxvii) "PROTEASOME SUBUNIT BETA TYPE 3" (SEQ ID No:37) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PROTEASOME SUBUNIT BETA TYPE 3" encoded by a nucleic acid that hybridizes to the "PROTEASOME SUBUNIT BETA TYPE 3" nucleic acid or its complement under low stringency conditions, (xxxviii) "Pot (SEQ ID No:38) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Pot1 " encoded by a nucleic acid that hybridizes to the "Pot1 " nucleic acid or its complement under low stringency conditions,

(xxxix) "RAD50 HOMOLOGUE HSRAD50" (SEQ ID No:39) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "RAD50 HOMOLOGUE HSRAD50" encoded by a nucleic acid that hybridizes to the "RAD50 HOMOLOGUE HSRAD50" nucleic acid or its complement under low stringency conditions,

(xl) "RAS GTPASE-ACTIVATING-LIKE PROTEIN IQGAP2" (SEQ ID No:40) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "RAS GTPASE-ACTIVATING-LIKE PROTEIN IQGAP2" encoded by a nucleic acid that hybridizes to the "RAS GTPASE-ACTIVATING-LIKE PROTEIN IQGAP2" nucleic acid or its complement under low stringency conditions, (xli) "SERINE/THREONINE PROTEIN PHOSPHATASE PP1 -ALPHA 1 CATALYTIC SUBUNIT" (SEQ ID No:41) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SERINE/THREONINE PROTEIN PHOSPHATASE PP1 -ALPHA 1 CATALYTIC SUBUNIT" encoded by a nucleic acid that hybridizes to the "SERINE/THREONINE PROTEIN PHOSPHATASE PP1- ALPHA 1 CATALYTIC SUBUNIT" nucleic acid or its complement under low stringency conditions,

(xlii) "SERINE/THREONINE PROTEIN PHOSPHATASE PP1-BETA CATALYTIC SUBUNIT" (SEQ ID No:42) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SERINE/THREONINE PROTEIN PHOSPHATASE PP1-BETA CATALYTIC SUBUNIT" encoded by a nucleic acid that hybridizes to the "SERINE/THREONINE PROTEIN PHOSPHATASE PP1- BETA CATALYTIC SUBUNIT" nucleic acid or its complement under low stringency conditions,

(xliii) "SERINE/THREONINE PROTEIN PHOSPHATASE PP1 -GAMMA CATALYTIC SUBUNIT" (SEQ ID No:43) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SERINE/THREONINE PROTEIN PHOSPHATASE PP1 -GAMMA CATALYTIC SUBUNIT" encoded by a nucleic acid that hybridizes to the "SERINE/THREONINE PROTEIN PHOSPHATASE PP1- GAMMA CATALYTIC SUBUNIT" nucleic acid or its complement under low stringency conditions,

(xliv) "SIMILAR TO OROSOMUCOID 1 " (SEQ ID No:44) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SIMILAR TO OROSOMUCOID 1" encoded by a nucleic acid that hybridizes to the "SIMILAR TO OROSOMUCOID 1" nucleic acid or its complement under low stringency conditions,

(xlv) "SMC5 PROTEIN" (SEQ ID No:45) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SMC5

(xlvi) "SQUAMOUS CELL CARCINOMA ANTIGEN 1 " (SEQ ID No:46) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SQUAMOUS CELL CARCINOMA ANTIGEN 1 " encoded by a nucleic acid that hybridizes to the "SQUAMOUS CELL CARCINOMA ANTIGEN 1" nucleic acid or its complement under low stringency conditions,

(xlvii) "SUPPRESSOR OF G2 ALLELE OF SKP1 HOMOLOG" (SEQ ID No:47) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SUPPRESSOR OF G2 ALLELE OF SKP1 HOMOLOG" encoded by a nucleic acid that hybridizes to the "SUPPRESSOR OF G2 ALLELE OF

SKP1 HOMOLOG" nucleic acid or its complement under low stringency conditions,

(xiviii) "Serine/threonine proteine phosphatase 2A, catalytic subunit, beta isoform" (SEQ

(xlix) "Similar to diacylglycerol kinase delta" (SEQ ID No:49) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Similar to diacylglycerol kinase delta" encoded by a nucleic acid that hybridizes to the "Similar to diacylglycerol kinase delta" nucleic acid or its complement under low stringency conditions,

(I) "TELOMERASE-BINDING PROTEIN P23" (SEQ ID No:50) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TELOMERASE-BINDING PROTEIN P23" encoded by a nucleic acid that hybridizes to the "TELOMERASE-BINDING PROTEIN P23" nucleic acid or its complement under low stringency conditions,

(Ii) "TELOMERIC REPEAT BINDING FACTOR 2" (SEQ ID No:51) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TELOMERIC REPEAT BINDING FACTOR 2" encoded by a nucleic acid that hybridizes to the "TELOMERIC REPEAT BINDING FACTOR 2" nucleic acid or its complement under low stringency conditions,

(Iii) "TERF1 (TRFI)-INTERACTING NUCLEAR FACTOR 2" (SEQ ID No:52) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TERF1 (TRFI)-INTERACTING NUCLEAR FACTOR 2" encoded by a nucleic acid that hybridizes to the "TERF1 (TRFI)-INTERACTING NUCLEAR FACTOR 2" nucleic acid or its complement under low stringency conditions, (liii) "TRF1 " (SEQ ID No:53) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TRF1" encoded by a nucleic acid that hybridizes to the "TRF1" nucleic acid or its complement under low stringency conditions,

(liv) "TRF2-INTERACTING TELOMERIC RAP1 PROTEIN" (SEQ ID No:54) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TRF2-INTERACTING TELOMERIC RAP1 PROTEIN" encoded by a nucleic acid that hybridizes to the "TRF2-INTERACTING TELOMERIC RAP1 PROTEIN" nucleic acid or its complement under low stringency conditions, (Iv) "TRICARBOXYLATE TRANSPORT PROTEIN, MITOCHONDRIAL PRECURSOR" (SEQ ID No:55) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TRICARBOXYLATE TRANSPORT PROTEIN, MITOCHONDRIAL PRECURSOR" encoded by a nucleic acid that hybridizes to the "TRICARBOXYLATE TRANSPORT PROTEIN, MITOCHONDRIAL PRECURSOR" nucleic acid or its complement under low stringency conditions, (Ivi) "U5 SMALL NUCLEAR RIBONUCLEOPROTEIN 200 KDA HELICASE (FRAGMENT)" (SEQ ID No:56) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "U5 SMALL NUCLEAR RIBONUCLEOPROTEIN 200 KDA HELICASE (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "U5 SMALL NUCLEAR RIBONUCLEOPROTEIN 200 KDA HELICASE (FRAGMENT)" nucleic acid or its complement under low stringency conditions, and/or

(Ivii) "WD-REPEAT PROTEIN AN11 HOMOLOG" (SEQ ID No:57) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "WD-REPEAT PROTEIN AN11 HOMOLOG" encoded by a nucleic acid that hybridizes to the "WD-REPEAT PROTEIN AN11 HOMOLOG" nucleic acid or its complement under low stringency conditions, and a protein complex selected from complex (II) and comprising the following proteins: (i) "38 KDA FK-506 BINDING PROTEIN HOMOLOG" (SEQ ID No:1) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "38 KDA FK-506 BINDING PROTEIN HOMOLOG" encoded by a nucleic acid that hybridizes to the "38 KDA FK-506 BINDING PROTEIN HOMOLOG" nucleic acid or its complement under low stringency conditions,

(xii) "CDNA: FLJ21908 FIS, CLONE HEP03830" (SEQ ID No: 12) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA: FLJ21908 FIS, CLONE HEP03830" encoded by a nucleic acid that hybridizes to the "CDNA: FLJ21908 FIS, CLONE HEP03830" nucleic acid or its complement under low stringency conditions, (xiii) "CENP-F KINETOCHORE PROTEIN" (SEQ ID No:13) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CENP-F KINETOCHORE PROTEIN" encoded by a nucleic acid that hybridizes to the "CENP-F KINETOCHORE PROTEIN" nucleic acid or its complement under low stringency conditions,

SUBUNIT C" nucleic acid or its complement under low stringency conditions,

SUBUNIT" encoded by a nucleic acid that hybridizes to the "DNA-DEPENDENT

POLYPEPTIDE" encoded by a nucleic acid that hybridizes to the "DNA-DIRECTED RNA

POLYMERASE II 23 KDA POLYPEPTIDE" nucleic acid or its complement under low stringency conditions,

(xxii) "HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN H"' (SEQ ID No:22) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN H"' encoded by a nucleic acid that hybridizes to the "HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN H'" nucleic acid or its complement under low stringency conditions,

(xxv) "HYPOTHETICAL PROTEIN KIAA0310 (FRAGMENT)" (SEQ ID No:25) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYPOTHETICAL PROTEIN KIAA0310 (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "HYPOTHETICAL PROTEIN KIAA0310 (FRAGMENT)" nucleic acid or its complement under low stringency conditions, (xxvi) "INCOMPATIBILITY PROTEIN HET-E-1 (FRAGMENT)" (SEQ ID No:26) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "INCOMPATIBILITY PROTEIN HET-E-1 (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "INCOMPATIBILITY PROTEIN HET-E-1

(FRAGMENT)" nucleic acid or its complement under low stringency conditions,

(xxviii) "KIAA1284 PROTEIN (FRAGMENT)" (SEQ ID No:28) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA1 84 PROTEIN (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "KIAA1284 PROTEIN (FRAGMENT)" nucleic acid or its complement under low stringency conditions,

(xxxii) "NEIGHBOR OF A-KINASE ANCHORING PROTEIN 95" (SEQ ID No:32) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "NEIGHBOR OF A-KINASE ANCHORING PROTEIN 95" encoded by a nucleic acid that hybridizes to the "NEIGHBOR OF A-KINASE

ANCHORING PROTEIN 95" nucleic acid or its complement under low stringency conditions,

(xxxvii) "PROTEASOME SUBUNIT BETA TYPE 3" (SEQ ID No:37) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PROTEASOME SUBUNIT BETA TYPE 3" encoded by a nucleic acid that hybridizes to the "PROTEASOME SUBUNIT BETA TYPE 3" nucleic acid or its complement under low stringency conditions,

(xxxviii) "Pot1 " (SEQ ID No:38) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Pot1 " encoded by a nucleic acid that hybridizes to the "Pot1 " nucleic acid or its complement under low stringency conditions,

(xliv) "SIMILAR TO OROSOMUCOID 1 " (SEQ ID No:44) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SIMILAR TO OROSOMUCOID 1 " encoded by a nucleic acid that hybridizes to the "SIMILAR TO OROSOMUCOID 1 " nucleic acid or its complement under low stringency conditions,

(xlv) "SMC5 PROTEIN" (SEQ ID No:45) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SMC5 PROTEIN" encoded by a nucleic acid that hybridizes to the "SMC5 PROTEIN" nucleic acid or its complement under low stringency conditions, (xlvi) "SQUAMOUS CELL CARCINOMA ANTIGEN 1 " (SEQ ID No:46) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SQUAMOUS CELL CARCINOMA ANTIGEN 1 " encoded by a nucleic acid that hybridizes to the "SQUAMOUS CELL CARCINOMA ANTIGEN 1 " nucleic acid or its complement under low stringency conditions,

(xlvii) "SUPPRESSOR OF G2 ALLELE OF SKP1 HOMOLOG" (SEQ ID No:47) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SUPPRESSOR OF G2 ALLELE OF SKP1 HOMOLOG" encoded by a nucleic acid that hybridizes to the "SUPPRESSOR OF G2 ALLELE OF SKP1 HOMOLOG" nucleic acid or its complement under low stringency conditions, (xlviii) "Serine/threonine proteine phosphatase 2A, catalytic subunit, beta isoform" (SEQ ID No:48) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Serine/threonine proteine phosphatase 2A, catalytic subunit, beta isoform" encoded by a nucleic acid that hybridizes to the "Serine/threonine proteine phosphatase 2A, catalytic subunit, beta isoform" nucleic acid or its complement under low stringency conditions,

(Iii) "TERF1 (TRFI)-INTERACTING NUCLEAR FACTOR 2" (SEQ ID No:52) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TERF1 (TRFI)-INTERACTING NUCLEAR FACTOR 2" encoded by a nucleic acid that hybridizes to the "TERF1 (TRFI)-INTERACTING NUCLEAR FACTOR 2" nucleic acid or its complement under low stringency conditions, (liii) "TRF1 " (SEQ ID No:53) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TRF1 " encoded by a nucleic acid that hybridizes to the "TRF1 " nucleic acid or its complement under low stringency conditions,

(Ivii) "WD-REPEAT PROTEIN AN11 HOMOLOG" (SEQ ID No:57) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "WD-REPEAT PROTEIN AN11 HOMOLOG" encoded by a nucleic acid that hybridizes to the "WD-REPEAT PROTEIN AN11 HOMOLOG" nucleic acid or its complement under low stringency conditions, and a protein complex selected from complex (III) and comprising the following proteins: (i) "38 KDA FK-506 BINDING PROTEIN HOMOLOG" (SEQ ID No:1) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "38 KDA FK-506 BINDING PROTEIN HOMOLOG" encoded by a nucleic acid that hybridizes to the "38 KDA FK-506 BINDING PROTEIN HOMOLOG" nucleic acid or its complement under low stringency conditions,

(v) "CASEIN KINASE II, ALPHA CHAIN" (SEQ ID No:6) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CASEIN KINASE II, ALPHA CHAIN" encoded by a nucleic acid that hybridizes to the "CASEIN KINASE II, ALPHA CHAIN" nucleic acid or its complement under low stringency conditions,

(vi) "CDNA FLJ13664 FIS, CLONE PLACE1011649" (SEQ ID No:7) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ13664 FIS, CLONE PLACE1011649" encoded by a nucleic acid that hybridizes to the "CDNA FLJ13664 FIS, CLONE PLACE1011649" nucleic acid or its complement under low stringency conditions,

(vii) "CDNA FLJ13998 FIS, CLONE Y79AA1002229" (SEQ ID No:8) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ13998 FIS, CLONE Y79AA1002229" encoded by a nucleic acid that hybridizes to the "CDNA FLJ13998 FIS, CLONE Y79AA1002229" nucleic acid or its complement under low stringency conditions,

(viii) "CDNA FLJ20643 FIS, CLONE KAT02633" (SEQ ID No:9) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ20643 FIS, CLONE KAT02633" encoded by a nucleic acid that hybridizes to the "CDNA FLJ20643 FIS, CLONE KAT02633" nucleic acid or its complement under low stringency conditions,

(ix) "CDNA FLJ31741 FIS, CLONE NT2RI2007148" (SEQ ID No:11) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ31741 FIS, CLONE NT2RI2007148" encoded by a nucleic acid that hybridizes to the "CDNA FLJ31741 FIS, CLONE NT2RI2007148" nucleic acid or its complement under low stringency conditions,

(x) "CDNA: FLJ21908 FIS, CLONE HEP03830" (SEQ ID No:12) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA: FLJ21908 FIS, CLONE HEP03830" encoded by a nucleic acid that hybridizes to the "CDNA: FLJ21908 FIS, CLONE HEP03830" nucleic acid or its complement under low stringency conditions,

(xi) "CHROMATIN ASSEMBLY FACTOR 1 SUBUNIT C" (SEQ ID No:14) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CHROMATIN ASSEMBLY FACTOR 1 SUBUNIT C" encoded by a nucleic acid that hybridizes to the "CHROMATIN ASSEMBLY FACTOR 1 SUBUNIT C" nucleic acid or its complement under low stringency conditions, (xii) "DNA MISMATCH REPAIR PROTEIN MSH6" (SEQ ID No:15) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "DNA MISMATCH REPAIR PROTEIN MSH6" encoded by a nucleic acid that hybridizes to the "DNA MISMATCH REPAIR PROTEIN MSH6" nucleic acid or its complement under low stringency conditions,

(xiii) "DNA-DEPENDENT PROTEIN KINASE CATALYTIC SUBUNIT" (SEQ ID No:16) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "DNA-DEPENDENT PROTEIN KINASE CATALYTIC SUBUNIT" encoded by a nucleic acid that hybridizes to the "DNA-DEPENDENT PROTEIN KINASE CATALYTIC SUBUNIT" nucleic acid or its complement under low stringency conditions,

(xiv) "DNA-DIRECTED RNA POLYMERASE II 23 KDA POLYPEPTIDE" (SEQ ID No:17) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "DNA-DIRECTED RNA POLYMERASE II 23 KDA POLYPEPTIDE" encoded by a nucleic acid that hybridizes to the "DNA-DIRECTED RNA POLYMERASE II 23 KDA POLYPEPTIDE" nucleic acid or its complement under low stringency conditions,

(xv) "GLIAL FIBRILLARY ACIDIC PROTEIN, ASTROCYTE" (SEQ ID No:20) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "GLIAL FIBRILLARY ACIDIC PROTEIN, ASTROCYTE" encoded by a nucleic acid that hybridizes to the "GLIAL FIBRILLARY ACIDIC PROTEIN, ASTROCYTE" nucleic acid or its complement under low stringency conditions, (xvi) "HDCMD34P" (SEQ ID No:21) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HDCMD34P" encoded by a nucleic acid that hybridizes to the "HDCMD34P" nucleic acid or its complement under low stringency conditions,

(xvii) "HISTONE ACETYLTRANSFERASE TYPE B SUBUNIT 2" (SEQ ID No:23) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HISTONE ACETYLTRANSFERASE TYPE B SUBUNIT 2" encoded by a nucleic acid that hybridizes to the "HISTONE ACETYLTRANSFERASE TYPE B SUBUNIT 2" nucleic acid or its complement under low stringency conditions,

(xviii) "KIAA1284 PROTEIN (FRAGMENT)" (SEQ ID No:28) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA1284 PROTEIN (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "KIAA1284 PROTEIN (FRAGMENT)" nucleic acid or its complement under low stringency conditions,

(xix) "MUTS" (SEQ ID No:30) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "MUTS" encoded by a nucleic acid that hybridizes to the "MUTS" nucleic acid or its complement under low stringency conditions,

(xx) "NEIGHBOR OF A-KINASE ANCHORING PROTEIN 95" (SEQ ID No:32) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "NEIGHBOR OF A-KINASE ANCHORING PROTEIN 95" encoded by a nucleic acid that hybridizes to the "NEIGHBOR OF A-KINASE ANCHORING PROTEIN 95" nucleic acid or its complement under low stringency conditions,

(xxi) "PROGRAMED CELL DEATH PROTEIN 2" (SEQ ID No:35) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PROGRAMED CELL DEATH PROTEIN 2" encoded by a nucleic acid that hybridizes to the "PROGRAMED CELL DEATH PROTEIN 2" nucleic acid or its complement under low stringency conditions,

(xxii) "Pot1 " (SEQ ID No:38) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Pot1 " encoded by a nucleic acid that hybridizes to the "Pot1 " nucleic acid or its complement under low stringency conditions,

(xxiii) "RAD50 HOMOLOGUE HSRAD50" (SEQ ID No:39) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "RAD50 HOMOLOGUE HSRAD50" encoded by a nucleic acid that hybridizes to the "RAD50 HOMOLOGUE HSRAD50" nucleic acid or its complement under low stringency conditions,

(xxiv) "RAS GTPASE-ACTIVATING-LIKE PROTEIN IQGAP2" (SEQ ID No:40) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "RAS GTPASE-ACTIVATING-LIKE PROTEIN IQGAP2" encoded by a nucleic acid that hybridizes to the "RAS GTPASE-ACTIVATING-LIKE PROTEIN IQGAP2" nucleic acid or its complement under low stringency conditions, (xxv) "SERINE/THREONINE PROTEIN PHOSPHATASE PP1 -ALPHA 1 CATALYTIC SUBUNIT" (SEQ ID No:41) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SERINE/THREONINE PROTEIN PHOSPHATASE PP1 -ALPHA 1 CATALYTIC SUBUNIT" encoded by a nucleic acid that hybridizes to the "SERINE/THREONINE PROTEIN PHOSPHATASE PP1- ALPHA 1 CATALYTIC SUBUNIT" nucleic acid or its complement under low stringency conditions,

(xxvi) "SERINE/THREONINE PROTEIN PHOSPHATASE PP1-BETA CATALYTIC SUBUNIT" (SEQ ID No:42) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SERINE/THREONINE PROTEIN PHOSPHATASE PP1-BETA CATALYTIC SUBUNIT" encoded by a nucleic acid that hybridizes to the "SERINE/THREONINE PROTEIN PHOSPHATASE PP1- BETA CATALYTIC SUBUNIT" nucleic acid or its complement under low stringency conditions,

(xxvii) "SERINE THREONINE PROTEIN PHOSPHATASE PP1 -GAMMA CATALYTIC SUBUNIT" (SEQ ID No:43) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SERINE/THREONINE PROTEIN PHOSPHATASE PP1 -GAMMA CATALYTIC SUBUNIT" encoded by a nucleic acid that hybridizes to the "SERINE THREONINE PROTEIN PHOSPHATASE PP1- GAMMA CATALYTIC SUBUNIT" nucleic acid or its complement under low stringency conditions,

(xxviii) "SQUAMOUS CELL CARCINOMA ANTIGEN 1 " (SEQ ID No:46) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SQUAMOUS CELL CARCINOMA ANTIGEN 1 " encoded by a nucleic acid that hybridizes to the "SQUAMOUS CELL CARCINOMA ANTIGEN 1 " nucleic acid or its complement under low stringency conditions,

(xxix) "SUPPRESSOR OF G2 ALLELE OF SKP1 HOMOLOG" (SEQ ID No:47) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SUPPRESSOR OF G2 ALLELE OF SKP1 HOMOLOG" encoded by a nucleic acid that hybridizes to the "SUPPRESSOR OF G2 ALLELE OF SKP1 HOMOLOG" nucleic acid or its complement under low stringency conditions, (xxx) "Serine/threonine proteine phosphatase 2A, catalytic subunit, beta isoform" (SEQ ID No:48) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Serine/threonine proteine phosphatase 2A, catalytic subunit, beta isoform" encoded by a nucleic acid that hybridizes to the "Serine/threonine proteine phosphatase 2A, catalytic subunit, beta isoform" nucleic acid or its complement under low stringency conditions,

(xxxi) "TELOMERASE-BINDING PROTEIN P23" (SEQ ID No:50) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TELOMERASE-BINDING PROTEIN P23" encoded by a nucleic acid that hybridizes to the "TELOMERASE-BINDING PROTEIN P23" nucleic acid or its complement under low stringency conditions,

(xxxii) "TELOMERIC REPEAT BINDING FACTOR 2" (SEQ ID No:51) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TELOMERIC REPEAT BINDING FACTOR 2" encoded by a nucleic acid that hybridizes to the "TELOMERIC REPEAT BINDING FACTOR 2" nucleic acid or its complement under low stringency conditions,

(xxxiii) "TERF1 (TRFI)-INTERACTING NUCLEAR FACTOR 2" (SEQ ID No:52) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TERF1 (TRFI)-INTERACTING NUCLEAR FACTOR 2" encoded by a nucleic acid that hybridizes to the "TERF1 (TRFI)-INTERACTING NUCLEAR FACTOR 2" nucleic acid or its complement under low stringency conditions, (xxxiv) "TRF1 " (SEQ ID No:53) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TRF1 " encoded by a nucleic acid that hybridizes to the "TRF1" nucleic acid or its complement under low stringency conditions,

(xxxv) "TRF2-INTERACTING TELOMERIC RAP1 PROTEIN" (SEQ ID No:54) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TRF2-INTERACTING TELOMERIC RAP1 PROTEIN" encoded by a nucleic acid that hybridizes to the "TRF2-INTERACTING TELOMERIC RAP1 PROTEIN" nucleic acid or its complement under low stringency conditions, (xxxvi) "WD-REPEAT PROTEIN AN11 HOMOLOG" (SEQ ID No:57) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "WD-REPEAT PROTEIN AN11 HOMOLOG" encoded by a nucleic acid that hybridizes to the "WD-REPEAT PROTEIN AN11 HOMOLOG" nucleic acid or its complement under low stringency conditions,

4. The protein complex according to No. 1 comprising all but 1 - 55 of the following proteins:

(iii) "ATP-BINDING CASSETTE, SUB-FAMILY D, MEMBER 3" (SEQ ID No:3) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ATP-BINDING CASSETTE, SUB-FAMILY D, MEMBER 3" encoded by a nucleic acid that hybridizes to the "ATP-BINDING CASSETTE, SUBFAMILY D, MEMBER 3" nucleic acid or its complement under low stringency conditions, (iv) "ATP-DEPENDENT DNA HELICASE II, 80 KDA SUBUNIT" (SEQ ID No:4) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ATP-DEPENDENT DNA HELICASE II, 80 KDA

SUBUNIT" encoded by a nucleic acid that hybridizes to the "ATP-DEPENDENT DNA

CLONE TST00267 (FRAGMENT)" nucleic acid or its complement under low stringency conditions, (xi) "CDNA FLJ31741 FIS, CLONE NT2RI2007148" (SEQ ID No:11) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ31741 FIS, CLONE NT2RI2007148" encoded by a nucleic acid that hybridizes to the "CDNA FLJ31741 FIS, CLONE NT2RI2007148" nucleic acid or its complement under low stringency conditions,

SUBUNIT C" nucleic acid or its complement under low stringency conditions,

SUBUNIT" encoded by a nucleic acid that hybridizes to the "DNA-DEPENDENT

(FRAGMENT)" nucleic acid or its complement under low stringency conditions,

(xxviii) "KIAA1284 PROTEIN (FRAGMENT)" (SEQ ID No:28) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA1284 PROTEIN (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "KIAA1 84 PROTEIN (FRAGMENT)" nucleic acid or its complement under low stringency conditions,

(xxxvii) "PROTEASOME SUBUNIT BETA TYPE 3" (SEQ ID No:37) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PROTEASOME SUBUNIT BETA TYPE 3" encoded by a nucleic acid that hybridizes to the "PROTEASOME SUBUNIT BETA TYPE 3" nucleic acid or its complement under low stringency conditions, (xxxviii) "Pot1 " (SEQ ID No:38) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Pot1 " encoded by a nucleic acid that hybridizes to the "Pot1 " nucleic acid or its complement under low stringency conditions,

(xl) "RAS GTPASE-ACTIVATING-LIKE PROTEIN IQGAP2" (SEQ ID No:40) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "RAS GTPASE-ACTIVATING-LIKE PROTEIN IQGAP2" encoded by a nucleic acid that hybridizes to the "RAS GTPASE-ACTIVATING-LIKE PROTEIN IQGAP2" nucleic acid or its complement under low stringency conditions, (xli) "SERINE/THREONINE PROTEIN PHOSPHATASE PP1 -ALPHA 1 CATALYTIC SUBUNIT" (SEQ ID No:41) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SERINETHREONINE PROTEIN PHOSPHATASE PP1 -ALPHA 1 CATALYTIC SUBUNIT" encoded by a nucleic acid that hybridizes to the "SERINE/THREONINE PROTEIN PHOSPHATASE PP1- ALPHA 1 CATALYTIC SUBUNIT" nucleic acid or its complement under low stringency conditions,

(xlvi) "SQUAMOUS CELL CARCINOMA ANTIGEN 1" (SEQ ID No:46) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SQUAMOUS CELL CARCINOMA ANTIGEN 1 " encoded by a nucleic acid that hybridizes to the "SQUAMOUS CELL CARCINOMA ANTIGEN 1 " nucleic acid or its complement under low stringency conditions,

SKP1 HOMOLOG" nucleic acid or its complement under low stringency conditions,

(xlviii) "Serine/threonine proteine phosphatase 2A, catalytic subunit, beta isoform" (SEQ

(Iii) "TERF1 (TRFI)-INTERACTING NUCLEAR FACTOR 2" (SEQ ID No:52) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TERF1 (TRFI)-INTERACTING NUCLEAR FACTOR 2" encoded by a nucleic acid that hybridizes to the "TERF1 (TRFI)-INTERACTING NUCLEAR FACTOR 2" nucleic acid or its complement under low stringency conditions, (liii) "TRF1 " (SEQ ID No:53) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TRF1 " encoded by a nucleic acid that hybridizes to the "TRF1" nucleic acid or its complement under low stringency conditions,

(liv) "TRF2-INTERACTING TELOMERIC RAP1 PROTEIN" (SEQ ID No:54) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TRF2-INTERACTING TELOMERIC RAP1 PROTEIN" encoded by a nucleic acid that hybridizes to the "TRF2-INTERACTING TELOMERIC RAP1 PROTEIN" nucleic acid or its complement under low stringency conditions, (Iv) "TRICARBOXYLATE TRANSPORT PROTEIN, MITOCHONDRIAL PRECURSOR" (SEQ ID No:55) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TRICARBOXYLATE TRANSPORT PROTEIN, MITOCHONDRIAL PRECURSOR" encoded by a nucleic acid that hybridizes to the "TRICARBOXYLATE TRANSPORT PROTEIN, MITOCHONDRIAL PRECURSOR" nucleic acid or its complement under low stringency conditions, (Ivi) "U5 SMALL NUCLEAR RIBONUCLEOPROTEIN 200 KDA HELICASE (FRAGMENT)" (SEQ ID No:56) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "U5 SMALL NUCLEAR RIBONUCLEOPROTEIN 200 KDA HELICASE (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "U5 SMALL NUCLEAR RIBONUCLEOPROTEIN 200 KDA HELICASE (FRAGMENT)" nucleic acid or its complement under low stringency conditions,

(Ivii) "WD-REPEAT PROTEIN AN11 HOMOLOG" (SEQ ID No:57) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "WD-REPEAT PROTEIN AN11 HOMOLOG" encoded by a nucleic acid that hybridizes to the "WD-REPEAT PROTEIN AN11 HOMOLOG" nucleic acid or its complement under low stringency conditions.

5. The complex of any of No. 1 - 4 comprising a functionally active derivative of said first protein and/or a functionally active derivative of said second protein, wherein the functionally active derivative is a fusion protein comprising said first protein or said second protein fused to an amino acid sequence different from the first protein or second protein, respectively.

8. The complex of any of No. 1 - 7 that is involved in the DNA binding activity, TRF2 binding activity or RAP1 binding activity.

9. A process for preparing a complex of any of No. 1 - 8 and optionally the components thereof comprising the following steps:expressing a protein (bait) of the complex, preferably a tagged protein, in a target cell, isolating the protein complex which is attached to the bait protein, and optionally dissociating the protein complex and isolating the individual complex members.

10. The process according to No. 9 wherein the tagged protein comprises two different tags which allow two separate affinity purification steps. 11. The process according to any of No. 9 - 10 wherein the two tags are separated by a cleavage site for a protease.

12. Component of the telomere capping complex obtainable by a process according to any of No. 9 - 11.

13. Protein of the telomere capping complex selected from

(i) "CDNA FLJ13664 FIS, CLONE PLACE1011649" (SEQ ID No:7) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ13664 FIS, CLONE PLACE1011649" encoded by a nucleic acid that hybridizes to the "CDNA FLJ13664 FIS, CLONE PLACE1011649" nucleic acid or its complement under low stringency conditions,

(ii) "CDNA FLJ13998 FIS, CLONE Y79AA1002229" (SEQ ID No:8) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ 13998 FIS, CLONE Y79AA1002229" encoded by a nucleic acid that hybridizes to the "CDNA FLJ13998 FIS, CLONE Y79AA1002229" nucleic acid or its complement under low stringency conditions,

(iii) "CDNA FLJ20643 FIS, CLONE KAT02633" (SEQ ID No:9) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ20643 FIS, CLONE KAT02633" encoded by a nucleic acid that hybridizes to the "CDNA FLJ20643 FIS, CLONE KAT02633" nucleic acid or its complement under low stringency conditions,

(iv) "CDNA FLJ25320 FIS, CLONE TST00267 (FRAGMENT)" (SEQ ID No:10) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ25320 FIS, CLONE TST00267 (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "CDNA FLJ25320 FIS, CLONE TST00267 (FRAGMENT)" nucleic acid or its complement under low stringency conditions,

(v) "CDNA FLJ31741 FIS, CLONE NT2RI2007148" (SEQ ID No:11) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ31741 FIS, CLONE NT2RI2007148" encoded by a nucleic acid that hybridizes to the "CDNA FLJ31741 FIS, CLONE NT2RI2007148" nucleic acid or its complement under low stringency conditions, (vi) "CDNA: FLJ21908 FIS, CLONE HEP03830" (SEQ ID No: 12) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA: FLJ21908 FIS, CLONE HEP03830" encoded by a nucleic acid that hybridizes to the "CDNA: FLJ21908 FIS, CLONE HEP03830" nucleic acid or its complement under low stringency conditions,

(vii) "HSPC029" (SEQ ID No:24) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HSPC029" encoded by a nucleic acid that hybridizes to the "HSPC029" nucleic acid or its complement under low stringency conditions,

(viii) "HYPOTHETICAL PROTEIN KIAA0310 (FRAGMENT)" (SEQ ID No:25) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYPOTHETICAL PROTEIN KIAA0310 (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "HYPOTHETICAL PROTEIN KIAA0310 (FRAGMENT)" nucleic acid or its complement under low stringency conditions, (ix) "KIAA0792 PROTEIN" (SEQ ID No:27) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA0792 PROTEIN" encoded by a nucleic acid that hybridizes to the "KIAA0792 PROTEIN" nucleic acid or its complement under low stringency conditions,

(x) "KIAA1284 PROTEIN (FRAGMENT)" (SEQ ID No:28) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA1284 PROTEIN (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "KIAA1284 PROTEIN (FRAGMENT)" nucleic acid or its complement under low stringency conditions, and

(xi) "P30 DBC" (SEQ ID No:33) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "P30 DBC" encoded by a nucleic acid that hybridizes to the "P30 DBC" nucleic acid or its complement under low stringency conditions, wherein said low stringency conditions comprise hybridization in a buffer comprising 35% formamide, 5X SSC, 50 mM Tris-HCI (pH 7.5), 5 mM EDTA, 0.02% PVP, 0.02% Ficoll, 0.2% BSA, 100 ug/ml denatured salmon sperm DNA, and 10% (wt/vol) dextran sulfate for 18-20 hours at 40 Celsius, washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4), 5 mM EDTA, and 0.1 % SDS for 1.5 hours at 55 Celsius, and washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4), 5 mM EDTA, and 0.1% SDS for 1.5 hours at 60 Celsius. 14. Nucleic acid encoding a protein according to No. 13.

15. Construct, preferably a vector construct, comprising (a) a nucleic acid according to No. 14 and at least one further nucleic acid which is normally not associated with said nucleic acid, or

(b) at least two separate nucleic acid sequences each encoding a different protein, or a functionally active fragment or a functionally active derivative of at least one of said proteins, or functionally active fragments or functionally active derivative thereof being selected from the first group of proteins according to No. 1 (a) and at least one of said proteins, or functionally active fragments or functionally active derivative thereof being selected from the second group of proteins according to No. 1 (b).

16. Host cell, containing a vector comprising at least one of the nucleic acid of No. 14 and/or a construct of No. 15 or containing several vectors each comprising at least the nucleic acid sequence encoding at least one of the proteins, or functionally active fragments or functionally active derivatives thereof selected from the first group of proteins according to No. 1 (a) and the proteins, or functionally active fragments or functionally active derivatives thereof selected from the second group of proteins according to No. 1 (b).

17. An antibody or a fragment of said antibody containing the binding domain thereof, selected from an antibody or fragment thereof, which binds the complex of any of No. 1 - 8 and which does not bind any of the proteins of said complex when uncomplexed and an antibody or a fragment of said antibody which binds to any of the proteins according to No. 13.

18. A kit comprising in one or more container the complex of any of No. 1 - 8 and/or the proteins of No. 13 optionally together with an antibody according to No. 17 and/or further components such as reagents and working instructions.

19. The kit according to No. 18 for processing a substrate of said complex. 20. The kit according to No. 18 for the diagnosis or prognosis of a disease or a disease risk, preferentially for a disease or disorder such as cancer such as solid tumours such as breast cancer, prostate cancer, lung cancer, colon cancer;cancer such as haematological cancers such as leukemia.

21. Array, in which at least a complex according to any of No. 1 - 8 and/or at least one protein according to No. 14 and/or at least one antibody according to No. 17 is attached to a solid carrier.

22. A process for processing a physiological substrate of the complex comprising the step of bringing into contact a complex to any of No. 1 - 8 with said substrate, such that said substrate is processed.

23. A pharmaceutical composition comprising the protein complex of any of No. 1 - 8 and/or any of the following the proteins:

(ii) "CDNA FLJ13998 FIS, CLONE Y79AA1002229" (SEQ ID No:8) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ13998 FIS, CLONE Y79AA1002229" encoded by a nucleic acid that hybridizes to the "CDNA FLJ13998 FIS, CLONE Y79AA1002229" nucleic acid or its complement under low stringency conditions,

(v) "CDNA FLJ31741 FIS, CLONE NT2RI2007148" (SEQ ID No:11) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ31741 FIS, CLONE NT2RI2007148" encoded by a nucleic acid that hybridizes to the "CDNA FLJ31741 FIS, CLONE NT2RI2007148" nucleic acid or its complement under low stringency conditions,

(vi) "CDNA: FLJ21908 FIS, CLONE HEP03830" (SEQ ID No:12) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA: FLJ21908 FIS, CLONE HEP03830" encoded by a nucleic acid that hybridizes to the "CDNA: FLJ21908 FIS, CLONE HEP03830" nucleic acid or its complement under low stringency conditions,

(viii) "HYPOTHETICAL PROTEIN KIAA0310 (FRAGMENT)" (SEQ ID No:25) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYPOTHETICAL PROTEIN KIAA0310 (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "HYPOTHETICAL PROTEIN KIAA0310

(FRAGMENT)" nucleic acid or its complement under low stringency conditions,

(ix) "KIAA0792 PROTEIN" (SEQ ID No:27) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA0792

(x) "KIAA1284 PROTEIN (FRAGMENT)" (SEQ ID No:28) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA1284 PROTEIN (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "KIAA1284 PROTEIN (FRAGMENT)" nucleic acid or its complement under low stringency conditions, and/or

(xi) "P30 DBC" (SEQ ID No:33) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "P30 DBC" encoded by a nucleic acid that hybridizes to the "P30 DBC" nucleic acid or its complement under low stringency conditions, and a pharmaceutical acceptable carrier. 24. A pharmaceutical composition according to No. 23 for the treatment of diseases and disorders such as cancer such as solid tumours such as breast cancer, prostate cancer, lung cancer, colon cancer;cancer such as haematological cancers such as leukemia.

25. A method for screening for a molecule that binds to the complex of anyone of No. 1 - 8 and/or any of the following the proteins:

(vi) "CDNA: FLJ21908 FIS, CLONE HEP03830" (SEQ ID No: 12) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA: FLJ21908 FIS, CLONE HEP03830" encoded by a nucleic acid that hybridizes to the "CDNA: FLJ21908 FIS, CLONE HEP03830" nucleic acid or its complement under low stringency conditions,

(FRAGMENT)" nucleic acid or its complement under low stringency conditions,

(xi) "P30 DBC" (SEQ ID No:33) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "P30 DBC" encoded by a nucleic acid that hybridizes to the "P30 DBC" nucleic acid or its complement under low stringency conditions, comprising the steps of

(a) exposing said complex, or a cell or organism containing same to one or more candidate molecules; and

(b) determinig whether said candidate molecule is bound to the complex or protein. 26. A method for screening for a molecule that modulates directly or indirectly the function, activity, composition or formation of the complex of any one of No. 1 - 8 comprising the steps of(a) exposing said complex, or a cell or organism containing telomere capping complex to one or more candidate molecules; and

(b) determining the amount of activity of protein components of, and/or intracellular localization of, said complex and/or the transcription level of a gene dependent on the complex and/or the abundance and/or activity of a protein or protein complex dependent on the function of the complex and/or product of a gene dependent on the complex in the presence of the one or more candidate molecules, wherein a change in said amount, activity, protein components or intracellular localization relative to said amount, activity, protein components and/or intracellular localization and/or a change in the transcription level of a gene dependent on the complex and/or the abundance and/or activity of a protein or protein complex dependent on the function of the complex and/or product of a gene dependent on the complex in the absence of said candidate molecules indicates that the molecule modulates function, activity or composition of said complex.

27. The method of No. 26, wherein the amount of said complex is determined.

28. The method of No. 26, wherein the activity of said complex is determined.

29. The method of No. 28, wherein said determining step comprises isolating from the cell or organism said complex to produce said isolated complex and contacting said isolated complex in the presence or absence of a candidate molecule with a substrate of said complex and determining the processing of said substrate is modified in the presence of said candidate molecule.

30. The method of No. 26, wherein the amount of the individual protein components of said complex are determined.

31. The method of No. 30, wherein said determining step comprises determining whether (i) "38 KDA FK-506 BINDING PROTEIN HOMOLOG" (SEQ ID No:1) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "38 KDA FK-506 BINDING PROTEIN HOMOLOG" encoded by a nucleic acid that hybridizes to the "38 KDA FK-506 BINDING PROTEIN HOMOLOG" nucleic acid or its complement under low stringency conditions, and/or

(ii) "ANTIGEN NY-CO-7" (SEQ ID No:2) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ANTIGEN NY- CO-7" encoded by a nucleic acid that hybridizes to the "ANTIGEN NY-CO-7" nucleic acid or its complement under low stringency conditions, and/or

(iii) "ATP-BINDING CASSETTE, SUB-FAMILY D, MEMBER 3" (SEQ ID No:3) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ATP-BINDING CASSETTE, SUB-FAMILY D, MEMBER 3" encoded by a nucleic acid that hybridizes to the "ATP-BINDING CASSETTE, SUBFAMILY D, MEMBER 3" nucleic acid or its complement under low stringency conditions, and/or

(iv) "ATP-DEPENDENT DNA HELICASE II, 80 KDA SUBUNIT" (SEQ ID No:4) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ATP-DEPENDENT DNA HELICASE II, 80 KDA SUBUNIT" encoded by a nucleic acid that hybridizes to the "ATP-DEPENDENT DNA HELICASE II, 80 KDA SUBUNIT" nucleic acid or its complement under low stringency conditions, and/or

(v) "BAF180" (SEQ ID No:5) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "BAF180" encoded by a nucleic acid that hybridizes to the "BAF180" nucleic acid or its complement under low stringency conditions, and/or

(vi) "CASEIN KINASE II, ALPHA CHAIN" (SEQ ID No:6) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CASEIN KINASE II, ALPHA CHAIN" encoded by a nucleic acid that hybridizes to the "CASEIN KINASE II, ALPHA CHAIN" nucleic acid or its complement under low stringency conditions, and/or

(vii) "CDNA FLJ13664 FIS, CLONE PLACE1011649" (SEQ ID No:7) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ13664 FIS, CLONE PLACE1011649" encoded by a nucleic acid that hybridizes to the "CDNA FLJ13664 FIS, CLONE PLACE1011649" nucleic acid or its complement under low stringency conditions, and/or

(viii) "CDNA FLJ13998 FIS, CLONE Y79AA1002229" (SEQ ID No:8) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ13998 FIS, CLONE Y79AA1002229" encoded by a nucleic acid that hybridizes to the "CDNA FLJ13998 FIS, CLONE Y79AA1002229" nucleic acid or its complement under low stringency conditions, and/or

(ix) "CDNA FLJ20643 FIS, CLONE KAT02633" (SEQ ID No:9) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ20643 FIS, CLONE KAT02633" encoded by a nucleic acid that hybridizes to the "CDNA FLJ20643 FIS, CLONE KAT02633" nucleic acid or its complement under low stringency conditions, and/or

CLONE TST00267 (FRAGMENT)" nucleic acid or its complement under low stringency conditions, and/or

(xi) "CDNA FLJ31741 FIS, CLONE NT2RI2007148" (SEQ ID No:11) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ31741 FIS, CLONE NT2RI2007148" encoded by a nucleic acid that hybridizes to the "CDNA FLJ31741 FIS, CLONE NT2RI2007148" nucleic acid or its complement under low stringency conditions, and/or

(xii) "CDNA: FLJ21908 FIS, CLONE HEP03830" (SEQ ID No:12) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA: FLJ21908 FIS, CLONE HEP03830" encoded by a nucleic acid that hybridizes to the "CDNA: FLJ21908 FIS, CLONE HEP03830" nucleic acid or its complement under low stringency conditions, and/or

(xiii) "CENP-F KINETOCHORE PROTEIN" (SEQ ID No:13) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CENP-F KINETOCHORE PROTEIN" encoded by a nucleic acid that hybridizes to the "CENP-F KINETOCHORE PROTEIN" nucleic acid or its complement under low stringency conditions, and/or

SUBUNIT C" nucleic acid or its complement under low stringency conditions, and/or (xv) "DNA MISMATCH REPAIR PROTEIN MSH6" (SEQ ID No:15) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "DNA MISMATCH REPAIR PROTEIN MSH6" encoded by a nucleic acid that hybridizes to the "DNA MISMATCH REPAIR PROTEIN MSH6" nucleic acid or its complement under low stringency conditions, and/or

(xvi) "DNA-DEPENDENT PROTEIN KINASE CATALYTIC SUBUNIT" (SEQ ID No:16) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "DNA-DEPENDENT PROTEIN KINASE CATALYTIC SUBUNIT" encoded by a nucleic acid that hybridizes to the "DNA-DEPENDENT PROTEIN KINASE CATALYTIC SUBUNIT" nucleic acid or its complement under low stringency conditions, and/or

(xvii) "DNA-DIRECTED RNA POLYMERASE II 23 KDA POLYPEPTIDE" (SEQ ID No:17) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "DNA-DIRECTED RNA POLYMERASE II 23 KDA POLYPEPTIDE" encoded by a nucleic acid that hybridizes to the "DNA-DIRECTED RNA POLYMERASE II 23 KDA POLYPEPTIDE" nucleic acid or its complement under low stringency conditions, and/or

(xviii) "ELONGATION FACTOR 2 KINASE" (SEQ ID No:18) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ELONGATION FACTOR 2 KINASE" encoded by a nucleic acid that hybridizes to the "ELONGATION FACTOR 2 KINASE" nucleic acid or its complement under low stringency conditions, and/or

(xix) "FK506-B1NDING PROTEIN 4" (SEQ ID No:19) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "FK506-BIND1NG PROTEIN 4" encoded by a nucleic acid that hybridizes to the "FK506- BINDING PROTEIN 4" nucleic acid or its complement under low stringency conditions, and/or

(xx) "GLIAL FIBRILLARY ACIDIC PROTEIN, ASTROCYTE" (SEQ ID No:20) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "GLIAL FIBRILLARY ACIDIC PROTEIN, ASTROCYTE" encoded by a nucleic acid that hybridizes to the "GLIAL FIBRILLARY ACIDIC PROTEIN, ASTROCYTE" nucleic acid or its complement under low stringency conditions, and/or (xxi) "HDCMD34P" (SEQ ID No:21) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HDCMD34P" encoded by a nucleic acid that hybridizes to the "HDCMD34P" nucleic acid or its complement under low stringency conditions, and/or

(xxii) "HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN H'" (SEQ ID No:22) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN H'" encoded by a nucleic acid that hybridizes to the "HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN H"' nucleic acid or its complement under low stringency conditions, and/or

(xxiii) "HISTONE ACETYLTRANSFERASE TYPE B SUBUNIT 2" (SEQ ID No:23) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HISTONE ACETYLTRANSFERASE TYPE B SUBUNIT 2" encoded by a nucleic acid that hybridizes to the "HISTONE ACETYLTRANSFERASE TYPE B SUBUNIT 2" nucleic acid or its complement under low stringency conditions, and/or

(xxiv) "HSPC029" (SEQ ID No:24) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HSPC029" encoded by a nucleic acid that hybridizes to the "HSPC029" nucleic acid or its complement under low stringency conditions, and/or

(xxv) "HYPOTHETICAL PROTEIN KIAA0310 (FRAGMENT)" (SEQ ID No:25) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYPOTHETICAL PROTEIN KIAA0310 (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "HYPOTHETICAL PROTEIN KIAA0310 (FRAGMENT)" nucleic acid or its complement under low stringency conditions, and/or (xxvi) "INCOMPATIBILITY PROTEIN HET-E-1 (FRAGMENT)" (SEQ ID No:26) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "INCOMPATIBILITY PROTEIN HET-E-1 (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "INCOMPATIBILITY PROTEIN HET-E-1 (FRAGMENT)" nucleic acid or its complement under low stringency conditions, and/or (xxvii) "KIAA0792 PROTEIN" (SEQ ID No:27) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA0792 PROTEIN" encoded by a nucleic acid that hybridizes to the "KIAA0792 PROTEIN" nucleic acid or its complement under low stringency conditions, and/or (xxviii) "KIAA1284 PROTEIN (FRAGMENT)" (SEQ ID No:28) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA1284 PROTEIN (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "KIAA1284 PROTEIN (FRAGMENT)" nucleic acid or its complement under low stringency conditions, and/or

(xxix) "MEPRIN A BETA-SUBUNIT PRECURSOR" (SEQ ID No:29) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "MEPRIN A BETA-SUBUNIT PRECURSOR" encoded by a nucleic acid that hybridizes to the "MEPRIN A BETA-SUBUNIT PRECURSOR" nucleic acid or its complement under low stringency conditions, and/or

(xxx) "MUTS" (SEQ ID No:30) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "MUTS" encoded by a nucleic acid that hybridizes to the "MUTS" nucleic acid or its complement under low stringency conditions, and/or

(xxxi) "MYELOID LEUKEMIA FACTOR 2" (SEQ ID No:31) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "MYELOID LEUKEMIA FACTOR 2" encoded by a nucleic acid that hybridizes to the "MYELOID LEUKEMIA FACTOR 2" nucleic acid or its complement under low stringency conditions, and/or

(xxxii) "NEIGHBOR OF A-KINASE ANCHORING PROTEIN 95" (SEQ ID No:32) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "NEIGHBOR OF A-KINASE ANCHORING PROTEIN 95" encoded by a nucleic acid that hybridizes to the "NEIGHBOR OF A-KINASE ANCHORING PROTEIN 95" nucleic acid or its complement under low stringency conditions, and/or

(xxxiii) "P30 DBC" (SEQ ID No:33) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "P30 DBC" encoded by a nucleic acid that hybridizes to the "P30 DBC" nucleic acid or its complement under low stringency conditions, and/or

(xxxiv) "PROBABLE UBIQUITIN CARBOXYL-TERMINAL HYDROLASE FAF-X" (SEQ ID No:34) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PROBABLE UBIQUITIN CARBOXYL- TERMINAL HYDROLASE FAF-X" encoded by a nucleic acid that hybridizes to the "PROBABLE UBIQUITIN CARBOXYL-TERMINAL HYDROLASE FAF-X" nucleic acid or its complement under low stringency conditions, and/or (xxxv) "PROGRAMED CELL DEATH PROTEIN 2" (SEQ ID No:35) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PROGRAMED CELL DEATH PROTEIN 2" encoded by a nucleic acid that hybridizes to the "PROGRAMED CELL DEATH PROTEIN 2" nucleic acid or its complement under low stringency conditions, and/or

(xxxvi) "PROLIFERATING CELL NUCLEAR ANTIGEN" (SEQ ID No:36) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PROLIFERATING CELL NUCLEAR ANTIGEN" encoded by a nucleic acid that hybridizes to the "PROLIFERATING CELL NUCLEAR ANTIGEN" nucleic acid or its complement under low stringency conditions, and/or

(xxxvii) "PROTEASOME SUBUNIT BETA TYPE 3" (SEQ ID No:37) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PROTEASOME SUBUNIT BETA TYPE 3" encoded by a nucleic acid that hybridizes to the "PROTEASOME SUBUNIT BETA TYPE 3" nucleic acid or its complement under low stringency conditions, and/or

(xxxviii) "Pot1" (SEQ ID No:38) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Pot1" encoded by a nucleic acid that hybridizes to the "Pot1" nucleic acid or its complement under low stringency conditions, and/or

(xxxix) "RAD50 HOMOLOGUE HSRAD50" (SEQ ID No:39) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "RAD50 HOMOLOGUE HSRAD50" encoded by a nucleic acid that hybridizes to the "RAD50 HOMOLOGUE HSRAD50" nucleic acid or its complement under low stringency conditions, and/or

(xl) "RAS GTPASE-ACTIVATING-LIKE PROTEIN IQGAP2" (SEQ ID No:40) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "RAS GTPASE-ACTIVATING-LIKE PROTEIN IQGAP2" encoded by a nucleic acid that hybridizes to the "RAS GTPASE-ACTIVATING-LIKE

PROTEIN IQGAP2" nucleic acid or its complement under low stringency conditions, and/or

(xli) "SERINE/THREONINE PROTEIN PHOSPHATASE PP1 -ALPHA 1 CATALYTIC

SUBUNIT" (SEQ ID No:41) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SERINE/THREONINE

PROTEIN PHOSPHATASE PP1 -ALPHA 1 CATALYTIC SUBUNIT" encoded by a nucleic acid that hybridizes to the "SERINE/THREONINE PROTEIN PHOSPHATASE PP1-

ALPHA 1 CATALYTIC SUBUNIT" nucleic acid or its complement under low stringency conditions, and/or

(xlii) "SERINE/THREONINE PROTEIN PHOSPHATASE PP1-BETA CATALYTIC

SUBUNIT" (SEQ ID No:42) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SERINE/THREONINE

PROTEIN PHOSPHATASE PP1-BETA CATALYTIC SUBUNIT" encoded by a nucleic acid that hybridizes to the "SERINE/THREONINE PROTEIN PHOSPHATASE PP1-

BETA CATALYTIC SUBUNIT" nucleic acid or its complement under low stringency conditions, and/or

(xliii) "SERINE/THREONINE PROTEIN PHOSPHATASE PP1 -GAMMA CATALYTIC

SUBUNIT" (SEQ ID No:43) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SERINE/THREONINE

PROTEIN PHOSPHATASE PP1 -GAMMA CATALYTIC SUBUNIT" encoded by a nucleic acid that hybridizes to the "SERINE/THREONINE PROTEIN PHOSPHATASE PP1-

GAMMA CATALYTIC SUBUNIT" nucleic acid or its complement under low stringency conditions, and/or

(xliv) "SIMILAR TO OROSOMUCOID 1 " (SEQ ID No:44) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SIMILAR TO OROSOMUCOID 1 " encoded by a nucleic acid that hybridizes to the "SIMILAR TO OROSOMUCOID 1 " nucleic acid or its complement under low stringency conditions, and/or

PROTEIN" encoded by a nucleic acid that hybridizes to the "SMC5 PROTEIN" nucleic acid or its complement under low stringency conditions, and/or

(xlvi) "SQUAMOUS CELL CARCINOMA ANTIGEN 1 " (SEQ ID No:46) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SQUAMOUS CELL CARCINOMA ANTIGEN 1 " encoded by a nucleic acid that hybridizes to the "SQUAMOUS CELL CARCINOMA ANTIGEN 1" nucleic acid or its complement under low stringency conditions, and/or

SKP1 HOMOLOG" nucleic acid or its complement under low stringency conditions, and/or

"Serine/threonine proteine phosphatase 2A, catalytic subunit, beta isoform" nucleic acid or its complement under low stringency conditions, and/or

(xlix) "Similar to diacylglycerol kinase delta" (SEQ ID No:49) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Similar to diacylglycerol kinase delta" encoded by a nucleic acid that hybridizes to the "Similar to diacylglycerol kinase delta" nucleic acid or its complement under low stringency conditions, and/or

(I) "TELOMERASE-BINDING PROTEIN P23" (SEQ ID No:50) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TELOMERASE-BINDING PROTEIN P23" encoded by a nucleic acid that hybridizes to the "TELOMERASE-BINDING PROTEIN P23" nucleic acid or its complement under low stringency conditions, and/or

(Ii) "TELOMERIC REPEAT BINDING FACTOR 2" (SEQ ID No:51) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TELOMERIC REPEAT BINDING FACTOR 2" encoded by a nucleic acid that hybridizes to the "TELOMERIC REPEAT BINDING FACTOR 2" nucleic acid or its complement under low stringency conditions, and/or

(Hi) "TERF1 (TRFI)-INTERACTING NUCLEAR FACTOR 2" (SEQ ID No:52) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TERF1 (TRFI)-INTERACTING NUCLEAR FACTOR 2" encoded by a nucleic acid that hybridizes to the "TERF1 (TRFI)-INTERACTING

NUCLEAR FACTOR 2" nucleic acid or its complement under low stringency conditions, and/or

(liii) "TRF1 " (SEQ ID No:53) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TRF1 " encoded by a nucleic acid that hybridizes to the "TRF1 " nucleic acid or its complement under low stringency conditions, and/or (liv) "TRF2-INTERACTING TELOMERIC RAP1 PROTEIN" (SEQ ID No:54) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TRF2-INTERACTING TELOMERIC RAP1 PROTEIN" encoded by a nucleic acid that hybridizes to the "TRF2-INTERACTING TELOMERIC RAP1 PROTEIN" nucleic acid or its complement under low stringency conditions, and/or (Iv) "TRICARBOXYLATE TRANSPORT PROTEIN, MITOCHONDRIAL PRECURSOR" (SEQ ID No:55) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TRICARBOXYLATE TRANSPORT PROTEIN, MITOCHONDRIAL PRECURSOR" encoded by a nucleic acid that hybridizes to the "TRICARBOXYLATE TRANSPORT PROTEIN, MITOCHONDRIAL PRECURSOR" nucleic acid or its complement under low stringency conditions, and/or (Ivi) "U5 SMALL NUCLEAR RIBONUCLEOPROTEIN 200 KDA HELICASE (FRAGMENT)" (SEQ ID No:56) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "U5 SMALL NUCLEAR RIBONUCLEOPROTEIN 200 KDA HELICASE (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "U5 SMALL NUCLEAR RIBONUCLEOPROTEIN 200 KDA HELICASE (FRAGMENT)" nucleic acid or its complement under low stringency conditions, and/or

(Ivii) "WD-REPEAT PROTEIN AN11 HOMOLOG" (SEQ ID No:57) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "WD-REPEAT PROTEIN AN11 HOMOLOG" encoded by a nucleic acid that hybridizes to the "WD-REPEAT PROTEIN AN11 HOMOLOG" nucleic acid or its complement under low stringency conditions, is present in the complex.

32. The method of any of No. 26 - 31 , wherein said method is a method of screening for a drug for treatment or prevention of a disease or disorder such as cancer such as solid tumours such as breast cancer, prostate cancer, lung cancer, colon cancer;cancer such as haematological cancers such as leukemia.

33. Use of a molecule that modulates the amount of, activity of, or the protein components of the complex of any one of No. 1 - 8 for the manufacture of a medicament for the treatment or prevention of a disease or disorder such as cancer such as solid tumours such as breast cancer, prostate cancer, lung cancer, colon cancer;cancer such as haematological cancers such as leukemia. 34. A method for the production of a pharmaceutical composition comprising carrying out the method of any of No. 1 - 8 to identify a molecule that modulates the function, activity, composition or formation of said complex, and further comprising mixing the identified molecule with a pharmaceutically acceptable carrier.

35. A method for diagnosing or screening for the presence of a disease or disorder or a predisposition for developing a disease or disorder in a subject, which disease or disorder is characterized by an aberrant amount of, activity of, or component composition of, or intracellular localization of the complex of any one of the No. 1 - 8, comprising determining the amount of, activity of, protein components of, and/or intracellular localization of, said complex and/or the transcription level of a gene dependent on the complex and/or the abundance and/or activity of a protein or protein complex dependent on the function of the complex and/or product of a gene dependent on the complex in a comparative sample derived from a subject, wherein a difference in said amount, activity, or protein components of, said complex in an analogous sample from a subject not having the disease or disorder or predisposition indicates the presence in the subject of the disease or disorder or predisposition in the subject.

36. The method of No. 35, wherein the amount of said complex is determined.

37. The method of No. 35, wherein the activity of said complex is determined.

38. The method of No. 37, wherein said determining step comprises isolating from the subject said complex to produce said isolated complex and contacting said isolated complex in the presence or absence of a candidate molecule with a substrate of said complex and determining whether said substrate is processed in the absence of the candidate molecule and whether the processing of said substrate is modified in the presence of said candidate molecule.

40. The method of No. 39, wherein said determining step comprises determining whether (i) "38 KDA FK-506 BINDING PROTEIN HOMOLOG" (SEQ ID No:1) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "38 KDA FK-506 BINDING PROTEIN HOMOLOG" encoded by a nucleic acid that hybridizes to the "38 KDA FK-506 BINDING PROTEIN HOMOLOG" nucleic acid or its complement under low stringency conditions, and/or

(x) "CDNA FLJ25320 FIS, CLONE TST00267 (FRAGMENT)" (SEQ ID No: 10) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ25320 FIS, CLONE TST00267

(xii) "CDNA: FLJ21908 FIS, CLONE HEP03830" (SEQ ID No: 12) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA: FLJ21908 FIS, CLONE HEP03830" encoded by a nucleic acid that hybridizes to the "CDNA: FLJ21908 FIS, CLONE HEP03830" nucleic acid or its complement under low stringency conditions, and/or

(xiii) "CENP-F KINETOCHORE PROTEIN" (SEQ ID No:13) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CENP-F KINETOCHORE PROTEIN" encoded by a nucleic acid that hybridizes to the "CENP-F KINETOCHORE PROTEIN" nucleic acid or its complement under low stringency conditions, and/or (xiv) "CHROMATIN ASSEMBLY FACTOR 1 SUBUNIT C" (SEQ ID No:14) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CHROMATIN ASSEMBLY FACTOR 1 SUBUNIT C" encoded by a nucleic acid that hybridizes to the "CHROMATIN ASSEMBLY FACTOR 1 SUBUNIT C" nucleic acid or its complement under low stringency conditions, and/or (xv) "DNA MISMATCH REPAIR PROTEIN MSH6" (SEQ ID No:15) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "DNA MISMATCH REPAIR PROTEIN MSH6" encoded by a nucleic acid that hybridizes to the "DNA MISMATCH REPAIR PROTEIN MSH6" nucleic acid or its complement under low stringency conditions, and/or

(xvi) "DNA-DEPENDENT PROTEIN KINASE CATALYTIC SUBUNIT" (SEQ ID No: 16) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "DNA-DEPENDENT PROTEIN KINASE CATALYTIC SUBUNIT" encoded by a nucleic acid that hybridizes to the "DNA-DEPENDENT PROTEIN KINASE CATALYTIC SUBUNIT" nucleic acid or its complement under low stringency conditions, and/or

(xix) "FK506-BINDING PROTEIN 4" (SEQ ID No:19) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "FK506-BINDING PROTEIN 4" encoded by a nucleic acid that hybridizes to the "FK506- BINDING PROTEIN 4" nucleic acid or its complement under low stringency conditions, and/or

(xxii) "HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN H'" (SEQ ID No:22) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN H'" encoded by a nucleic acid that hybridizes to the "HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN H'" nucleic acid or its complement under low stringency conditions, and/or

(xxv) "HYPOTHETICAL PROTEIN KIAA0310 (FRAGMENT)" (SEQ ID No:25) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYPOTHETICAL PROTEIN KIAA0310 (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "HYPOTHETICAL PROTEIN KIAA0310 (FRAGMENT)" nucleic acid or its complement under low stringency conditions, and/or (xxvi) "INCOMPATIBILITY PROTEIN HET-E-1 (FRAGMENT)" (SEQ ID No:26) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "INCOMPATIBILITY PROTEIN HET-E-1 (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "INCOMPATIBILITY PROTEIN HET-E-1 (FRAGMENT)" nucleic acid or its complement under low stringency conditions, and/or (xxvii) "KIAA0792 PROTEIN" (SEQ ID No:27) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA0792

PROTEIN" encoded by a nucleic acid that hybridizes to the "KIAA0792 PROTEIN" nucleic acid or its complement under low stringency conditions, and/or

(xxviii) "KIAA1284 PROTEIN (FRAGMENT)" (SEQ ID No:28) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA1284 PROTEIN (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "KIAA1284 PROTEIN (FRAGMENT)" nucleic acid or its complement under low stringency conditions, and/or

ANCHORING PROTEIN 95" nucleic acid or its complement under low stringency conditions, and/or

(xxxiii) "P30 DBC" (SEQ ID No:33) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "P30 DBC" encoded by a nucleic acid that hybridizes to the "P30 DBC" nucleic acid or its complement under low stringency conditions, and/or (xxxiv) "PROBABLE UBIQUITIN CARBOXYL-TERMINAL HYDROLASE FAF-X" (SEQ ID No:34) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PROBABLE UBIQUITIN CARBOXYL- TERMINAL HYDROLASE FAF-X" encoded by a nucleic acid that hybridizes to the "PROBABLE UBIQUITIN CARBOXYL-TERMINAL HYDROLASE FAF-X" nucleic acid or its complement under low stringency conditions, and/or

(xxxv) "PROGRAMED CELL DEATH PROTEIN 2" (SEQ ID No:35) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PROGRAMED CELL DEATH PROTEIN 2" encoded by a nucleic acid that hybridizes to the "PROGRAMED CELL DEATH PROTEIN 2" nucleic acid or its complement under low stringency conditions, and/or

(xxxviii) "Pot (SEQ ID No:38) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Pot1 " encoded by a nucleic acid that hybridizes to the "Pot1" nucleic acid or its complement under low stringency conditions, and/or

(xl) "RAS GTPASE-ACTIVATING-LIKE PROTEIN 1QGAP2" (SEQ ID No:40) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "RAS GTPASE-ACTIVATING-LIKE PROTEIN IQGAP2" encoded by a nucleic acid that hybridizes to the "RAS GTPASE-ACTIVATING-LIKE PROTEIN IQGAP2" nucleic acid or its complement under low stringency conditions, and/or

(xli) "SERINE/THREONINE PROTEIN PHOSPHATASE PP1 -ALPHA 1 CATALYTIC

(xlii) "SERINE/THREONINE PROTEIN PHOSPHATASE PP1-BETA CATALYTIC

(xliii) "SERINE/THREONINE PROTEIN PHOSPHATASE PP1 -GAMMA CATALYTIC

(xlvi) "SQUAMOUS CELL CARCINOMA ANTIGEN 1" (SEQ ID No:46) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SQUAMOUS CELL CARCINOMA ANTIGEN 1 " encoded by a nucleic acid that hybridizes to the "SQUAMOUS CELL CARCINOMA ANTIGEN 1 " nucleic acid or its complement under low stringency conditions, and/or

(Iii) "TERF1 (TRFI)-INTERACTING NUCLEAR FACTOR 2" (SEQ ID No:52) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TERF1 (TRFI)-INTERACTING NUCLEAR FACTOR 2" encoded by a nucleic acid that hybridizes to the "TERF1 (TRFI)-INTERACTING NUCLEAR FACTOR 2" nucleic acid or its complement under low stringency conditions, and/or

(liii) "TRF1 " (SEQ ID No:53) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TRF1 " encoded by a nucleic acid that hybridizes to the "TRF1 " nucleic acid or its complement under low stringency conditions, and/or

(liv) "TRF2-INTERACTING TELOMERIC RAP1 PROTEIN" (SEQ ID No:54) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TRF2-INTERACTING TELOMERIC RAP1 PROTEIN" encoded by a nucleic acid that hybridizes to the "TRF2-INTERACTING TELOMERIC RAP1 PROTEIN" nucleic acid or its complement under low stringency conditions, and/or (Iv) "TRICARBOXYLATE TRANSPORT PROTEIN, MITOCHONDRIAL PRECURSOR" (SEQ ID No:55) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TRICARBOXYLATE TRANSPORT PROTEIN, MITOCHONDRIAL PRECURSOR" encoded by a nucleic acid that hybridizes to the "TRICARBOXYLATE TRANSPORT PROTEIN, MITOCHONDRIAL PRECURSOR" nucleic acid or its complement under low stringency conditions, and/or (Ivi) "U5 SMALL NUCLEAR RIBONUCLEOPROTEIN 200 KDA HELICASE (FRAGMENT)" (SEQ ID No:56) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "U5 SMALL NUCLEAR RIBONUCLEOPROTEIN 200 KDA HELICASE (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "U5 SMALL NUCLEAR RIBONUCLEOPROTEIN 200 KDA HELICASE (FRAGMENT)" nucleic acid or its complement under low stringency conditions, and/or

(Ivii) "WD-REPEAT PROTEIN AN11 HOMOLOG" (SEQ ID No:57) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "WD-REPEAT PROTEIN AN11 HOMOLOG" encoded by a nucleic acid that hybridizes to the "WD-REPEAT PROTEIN AN11 HOMOLOG" nucleic acid or its complement under low stringency conditions.is present in the complex.

41. The complex of any one of No. 1 - 8, or proteins of No. 13 or the antibody or fragment of No. 17, for use in a method of diagnosing a disease or disorder such as cancer such as solid tumours such as breast cancer, prostate cancer, lung cancer, colon cancer;cancer such as haematological cancers such as leukemia.

42. A method for treating or preventing a disease or disorder characterized by an aberrant amount of, activity or component composition of or intracellular localization of, the complex of anyone of No. 1 - 8, comprising administering to a subject in need of such treatment or prevention a therapeutically effective amount of one or more molecules that modulate the amount of, DNA binding activity, TRF2 binding activity or RAP1 binding activity, or protein components of, said complex.

44. The method according to No. 42 , wherein said disease or disorder involves increased levels of the amount or activity of said complex.

45. Complex of any of No. 1 - 8 and/or protein selected from the following proteins

SUBUNIT C" nucleic acid or its complement under low stringency conditions,

SUBUNIT" encoded by a nucleic acid that hybridizes to the "DNA-DEPENDENT

(xix) "FK506-BINDING PROTEIN 4" (SEQ ID No:19) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "FK506-BINDING PROTEIN 4" encoded by a nucleic acid that hybridizes to the "FK506- BINDING PROTEIN 4" nucleic acid or its complement under low stringency conditions, (xx) "GLIAL FIBRILLARY ACIDIC PROTEIN, ASTROCYTE" (SEQ ID No:20) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "GLIAL FIBRILLARY ACIDIC PROTEIN, ASTROCYTE" encoded by a nucleic acid that hybridizes to the "GLIAL FIBRILLARY ACIDIC PROTEIN, ASTROCYTE" nucleic acid or its complement under low stringency conditions, (xxi) "HDCMD34P" (SEQ ID No:21) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HDCMD34P" encoded by a. nucleic acid that hybridizes to the "HDCMD34P" nucleic acid or its complement under low stringency conditions,

(xxv) "HYPOTHETICAL PROTEIN KIAA0310 (FRAGMENT)" (SEQ ID No:25) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYPOTHETICAL PROTEIN K1AA0310 (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "HYPOTHETICAL PROTEIN KIAA0310

(FRAGMENT)" nucleic acid or its complement under low stringency conditions,

(xlii) "SERINE/THREONINE PROTEIN PHOSPHATASE PP1-BETA CATALYTIC SUBUNIT" (SEQ ID No:42) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SERINETHREONINE PROTEIN PHOSPHATASE PP1-BETA CATALYTIC SUBUNIT" encoded by a nucleic acid that hybridizes to the "SERINE/THREONINE PROTEIN PHOSPHATASE PP1- BETA CATALYTIC SUBUNIT" nucleic acid or its complement under low stringency conditions,

(xliv) "SIMILAR TO OROSOMUCOID 1" (SEQ ID No:44) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SIMILAR TO OROSOMUCOID 1" encoded by a nucleic acid that hybridizes to the "SIMILAR TO OROSOMUCOID 1" nucleic acid or its complement under low stringency conditions,

(xlvi) "SQUAMOUS CELL CARCINOMA ANTIGEN 1 " (SEQ ID No:46) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SQUAMOUS CELL CARCINOMA ANTIGEN 1" encoded by a nucleic acid that hybridizes to the "SQUAMOUS CELL CARCINOMA ANTIGEN 1 " nucleic acid or its complement under low stringency conditions,

SKP1 HOMOLOG" nucleic acid or its complement under low stringency conditions,

(liv) "TRF2-INTERACTING TELOMERIC RAP1 PROTEIN" (SEQ ID No:54) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TRF2-INTERACTING TELOMERIC RAP1 PROTEIN" encoded by a nucleic acid that hybridizes to the "TRF2-INTERACTING TELOMERIC RAP1 PROTEIN" nucleic acid or its complement under low stringency conditions, (Iv) "TRICARBOXYLATE TRANSPORT PROTEIN, MITOCHONDRIAL PRECURSOR" (SEQ ID No:55) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TRICARBOXYLATE TRANSPORT PROTEIN, MITOCHONDRIAL PRECURSOR" encoded by a nucleic acid that hybridizes to the "TRICARBOXYLATE TRANSPORT PROTEIN, MITOCHONDRIAL PRECURSOR" nucleic acid or its complement under low stringency conditions, (Ivi) "U5 SMALL NUCLEAR RIBONUCLEOPROTEIN 200 KDA HELICASE (FRAGMENT)" (SEQ ID No:56) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "U5 SMALL NUCLEAR RIBONUCLEOPROTEIN 200 KDA HELICASE (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "U5 SMALL NUCLEAR RIBONUCLEOPROTEIN 200 KDA HELICASE (FRAGMENT)" nucleic acid or its complement under low stringency conditions, and/or(lvii) "WD-REPEAT PROTEIN AN11 HOMOLOG" (SEQ ID No:57) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "WD-REPEAT PROTEIN AN11 HOMOLOG" encoded by a nucleic acid that hybridizes to the "WD-REPEAT PROTEIN AN11 HOMOLOG" nucleic acid or its complement under low stringency conditions,as a target for an active agent of a pharmaceutical, preferably a drug target in the treatment or prevention of a disease or disorder such as cancer such as solid tumours such as breast cancer, prostate cancer, lung cancer, colon cancer;cancer such as haematological cancers such as leukemia.

Thus the invention further relates to the following embodiments of the Her2-protein complex

1. A protein complex selected from complex (I) and comprising

(a) at least one first protein selected from the group consisting of:

(i) "Grb2" (SEQ ID No:77) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Grb2" encoded by a nucleic acid that hybridizes to the "Grb2" nucleic acid or its complement under low stringency conditions,

(ii) "Heat shock protein 90, alpha" (SEQ ID No:83) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of

"Heat shock protein 90, alpha" encoded by a nucleic acid that hybridizes to the "Heat shock protein 90, alpha" nucleic acid or its complement under low stringency conditions,

(iii) "Her2" (SEQ ID No:84) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Her2" encoded by a nucleic acid that hybridizes to the "Her2" nucleic acid or its complement under low stringency conditions,

(iv) "Her4" (SEQ ID No:85) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Her4" encoded by a nucleic acid that hybridizes to the "Her4" nucleic acid or its complement under low stringency conditions,

(v) "PI3 kinase regulatory subunit p55 gamma" (SEQ ID No:90) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PI3 kinase regulatory subunit p55 gamma" encoded by a nucleic acid that hybridizes to the "PI3 kinase regulatory subunit p55 gamma" nucleic acid or its complement under low stringency conditions,

(vi) "PI3 kinase regulatory subunit p85 alpha" (SEQ ID No:91) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PI3 kinase regulatory subunit p85 alpha" encoded by a nucleic acid that hybridizes to the "PI3 kinase regulatory subunit p85 alpha" nucleic acid or its complement under low stringency conditions,

(vii) "PI3 kinase regulatory subunit p85 beta" (SEQ ID No:92) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PI3 kinase regulatory subunit p85 beta" encoded by a nucleic acid that hybridizes to the "PI3 kinase regulatory subunit p85 beta" nucleic acid or its complement under low stringency conditions,

(viii) "SHC" (SEQ ID No:96) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SHC" encoded by a nucleic acid that hybridizes to the "SHC" nucleic acid or its complement under low stringency conditions, and

(ix) "VAV-2" (SEQ ID No:104) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "VAV-2" encoded by a nucleic acid that hybridizes to the "VAV-2" nucleic acid or its complement under low stringency conditions, and

(i) "ALZHEIMER'S DISEASE AMYLOID A4 PROTEIN PRECURSOR" (SEQ ID No:58) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ALZHEIMER'S DISEASE AMYLOID A4 PROTEIN PRECURSOR" encoded by a nucleic acid that hybridizes to the "ALZHEIMER'S DISEASE AMYLOID A4 PROTEIN PRECURSOR" nucleic acid or its complement under low stringency conditions,

(ii) "ANCIENT UBIQUITOUS PROTEIN 1 PRECURSOR" (SEQ ID No:59) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ANCIENT UBIQUITOUS PROTEIN 1 PRECURSOR" encoded by a nucleic acid that hybridizes to the "ANCIENT UBIQUITOUS PROTEIN 1 PRECURSOR" nucleic acid or its complement under low stringency conditions, (iii) "ATP-DEPENDENT METALLOPROTEASE FTSH1 HOMOLOG" (SEQ ID No:60) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ATP-DEPENDENT METALLOPROTEASE FTSH1

HOMOLOG" encoded by a nucleic acid that hybridizes to the "ATP-DEPENDENT

METALLOPROTEASE FTSH1 HOMOLOG" nucleic acid or its complement under low stringency conditions,

(iv) "B-CELL RECEPTOR ASSOCIATED PROTEIN" (SEQ ID No:61) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "B-CELL RECEPTOR ASSOCIATED PROTEIN" encoded by a nucleic acid that hybridizes to the "B-CELL RECEPTOR ASSOCIATED PROTEIN" nucleic acid or its complement under low stringency conditions,

(v) "CDC37 HOMOLOG" (SEQ ID No:62) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDC37

HOMOLOG" encoded by a nucleic acid that hybridizes to the "CDC37 HOMOLOG" nucleic acid or its complement under low stringency conditions,

(vi) "CDNA FLJ12443 FIS, CLONE NT2RM1000186" (SEQ ID No:63) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ12443 FIS, CLONE NT2RM1000186" encoded by a nucleic acid that hybridizes to the "CDNA FLJ12443 FIS, CLONE NT2RM1000186" nucleic acid or its complement under low stringency conditions,

(vii) "CDNA FLJ12681 FIS, CLONE NT2RM4002446" (SEQ ID No:64) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ12681 FIS, CLONE NT2RM4002446" encoded by a nucleic acid that hybridizes to the "CDNA FLJ12681 FIS, CLONE NT2RM4002446" nucleic acid or its complement under low stringency conditions,

(viii) "CDNA FLJ13149 FIS, CLONE NT2RP3003344" (SEQ ID No:65) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ13149 FIS, CLONE NT2RP3003344" encoded by a nucleic acid that hybridizes to the "CDNA FLJ13149 FIS, CLONE NT2RP3003344" nucleic acid or its complement under low stringency conditions,

(ix) "CDNA FLJ13716 FIS, CLONE PLACE2000411 " (SEQ ID No:66) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ13716 FIS, CLONE PLACE2000411 " encoded by a nucleic acid that hybridizes to the "CDNA FLJ13716 FIS, CLONE PLACE2000411 " nucleic acid or its complement under low stringency conditions,

(x) "CDNA: FLJ22087 FIS, CLONE HEP15918" (SEQ ID No:67) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA: FLJ22087 FIS, CLONE HEP15918" encoded by a nucleic acid that hybridizes to the "CDNA: FLJ22087 FIS, CLONE HEP15918" nucleic acid or its complement under low stringency conditions,

(xi) "CDP-DIACYLGLYCEROL-INOSITOL 3-PHOSPHATIDYLTRANSFERASE" (SEQ ID No:68) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDP-DIACYLGLYCEROL-INOSITOL 3- PHOSPHATIDYLTRANSFERASE" encoded by a nucleic acid that hybridizes to the "CDP-DIACYLGLYCEROL-INOSITOL 3-PHOSPHATIDYLTRANSFERASE" nucleic acid or its complement under low stringency conditions,

(xii) "CHROMATIN-SPECIFIC TRANSCRIPTION ELONGATION FACTOR FACT 140 KDA SUBUNIT" (SEQ ID No:69) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CHROMATIN- SPECIFIC TRANSCRIPTION ELONGATION FACTOR FACT 140 KDA SUBUNIT" encoded by a nucleic acid that hybridizes to the "CHROMATIN-SPECIFIC TRANSCRIPTION ELONGATION FACTOR FACT 140 KDA SUBUNIT" nucleic acid or its complement, under low stringency conditions,

(xiii) "COLLAPSIN RESPONSE MEDIATOR PROTEIN-5" (SEQ ID No:70) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "COLLAPSIN RESPONSE MEDIATOR PROTEIN-5" encoded by a nucleic acid that hybridizes to the "COLLAPSIN RESPONSE MEDIATOR PROTEIN-5" nucleic acid or its complement under low stringency conditions, (xiv) "DIHYDROPYRIMIDINASE RELATED PROTEIN-5" (SEQ ID No:71) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "DIHYDROPYRIMIDINASE RELATED PROTEIN-5" encoded by a nucleic acid that hybridizes to the "DIHYDROPYRIMIDINASE RELATED PROTEIN-5" nucleic acid or its complement under low stringency conditions, (xv) "DOPAMINE-RESPONSIVE PROTEIN" (SEQ ID No:72) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "DOPAMINE-RESPONSIVE PROTEIN" encoded by a nucleic acid that hybridizes to the "DOPAMINE-RESPONSIVE PROTEIN" nucleic acid or its complement under low stringency conditions,

(xvi) "Diacylglycerol kinase epsilon" (SEQ ID No:73) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of

"Diacylglycerol kinase epsilon" encoded by a nucleic acid that hybridizes to the

"Diacylglycerol kinase epsilon" nucleic acid or its complement under low stringency conditions,

(xvii) "EXCITATORY AMINO ACID TRANSPORTER 1" (SEQ ID No:74) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "EXCITATORY AMINO ACID TRANSPORTER 1 " encoded by a nucleic acid that hybridizes to the "EXCITATORY AMINO ACID TRANSPORTER 1 " nucleic acid or its complement under low stringency conditions,

(xviii) "FILAMIN A" (SEQ ID No:75) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "FILAMIN A" encoded by a nucleic acid that hybridizes to the "FILAMIN A" nucleic acid or its complement under low stringency conditions,

(xix) "GPI8 PROTEIN (FRAGMENT)" (SEQ ID No:76) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of

"GPI8 PROTEIN (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "GPI8

PROTEIN (FRAGMENT)" nucleic acid or its complement under low stringency conditions,

(xx) "HPT PROTEIN PRECURSOR" (SEQ ID No:78) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of

"HPT PROTEIN PRECURSOR" encoded by a nucleic acid that hybridizes to the "HPT

PROTEIN PRECURSOR" nucleic acid or its complement under low stringency conditions,

(xxi) "HSGCN1 (FRAGMENT)" (SEQ ID No:79) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HSGCN1

(FRAGMENT)" encoded by a nucleic acid that hybridizes to the "HSGCN1

(FRAGMENT)" nucleic acid or its complement under low stringency conditions,

(xxii) "HYPOTHETICAL 35.7 KDA PROTEIN" (SEQ ID No:80) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYPOTHETICAL 35.7 KDA PROTEIN" encoded by a nucleic acid that hybridizes to the "HYPOTHETICAL 35.7 KDA PROTEIN" nucleic acid or its complement under low stringency conditions,

(xxiii) "HYPOTHETICAL 68.1 KDA PROTEIN" (SEQ ID No:81) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYPOTHETICAL 68.1 KDA PROTEIN" encoded by a nucleic acid that hybridizes to the "HYPOTHETICAL 68.1 KDA PROTEIN" nucleic acid or its complement under low stringency conditions,

(xxiv) "HYPOTHETICAL PROTEIN XP_058906" (SEQ ID No:82) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYPOTHETICAL PROTEIN XP_058906" encoded by a nucleic acid that hybridizes to the "HYPOTHETICAL PROTEIN XP_058906" nucleic acid or its complement under low stringency conditions,

(xxv) "INSULIN RECEPTOR SUBSTRATE 4" (SEQ ID No:86) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "INSULIN RECEPTOR SUBSTRATE 4" encoded by a nucleic acid that hybridizes to the "INSULIN RECEPTOR SUBSTRATE 4" nucleic acid or its complement under low stringency conditions,

(xxvi) "KIAA0667 PROTEIN (FRAGMENT)" (SEQ ID No:87) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA0667 PROTEIN (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "KIAA0667 PROTEIN (FRAGMENT)" nucleic acid or its complement under low stringency conditions,

(xxviii) "KIAA0887 PROTEIN (FRAGMENT)" (SEQ ID No:88) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA0887 PROTEIN (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "KIAA0887 PROTEIN (FRAGMENT)" nucleic acid or its complement under low stringency conditions,

(xxix) "PALMITOYL-PROTEIN THIOESTERASE 1 PRECURSOR" (SEQ ID No:89) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PALMITOYL-PROTEIN THIOESTERASE 1 PRECURSOR" encoded by a nucleic acid that hybridizes to the "PALMITOYL-PROTEIN THIOESTERASE 1 PRECURSOR" nucleic acid or its complement under low stringency conditions,

(xxx) "PROCOLLAGEN-PROLINE, 2-OXOGLUTARATE 4-DIOXYGENASE (PROLINE 4- HYDROXYLASE), ALPHA POLYPEPTIDE I" (SEQ ID No:93) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PROCOLLAGEN-PROLINE, 2-OXOGLUTARATE 4-DIOXYGENASE (PROLINE 4- HYDROXYLASE), ALPHA POLYPEPTIDE I" encoded by a nucleic acid that hybridizes to the "PROCOLLAGEN-PROLINE, 2-OXOGLUTARATE 4- DIOXYGENASE (PROLINE 4- HYDROXYLASE), ALPHA POLYPEPTIDE I" nucleic acid or its complement under low stringency conditions,

(xxxi) "RIBONUCLEOSIDE-DIPHOSPHATE REDUCTASE M2 CHAIN" (SEQ ID No:94) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "RIBONUCLEOSIDE-DIPHOSPHATE REDUCTASE M2 CHAIN" encoded by a nucleic acid that hybridizes to the "RIBONUCLEOSIDE- DIPHOSPHATE REDUCTASE M2 CHAIN" nucleic acid or its complement under low stringency conditions,

(xxxii) "SEL-1 HOMOLOG PRECURSOR" (SEQ ID No:95) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SEL-1 HOMOLOG PRECURSOR" encoded by a nucleic acid that hybridizes to the "SEL-1 HOMOLOG PRECURSOR" nucleic acid or its complement under low stringency conditions,

(xxxiii) "SIMILAR TO ADP.ATP CARRIER PROTEIN" (SEQ ID No:97) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SIMILAR TO ADP.ATP CARRIER PROTEIN" encoded by a nucleic acid that hybridizes to the "SIMILAR TO ADP.ATP CARRIER PROTEIN" nucleic acid or its complement under low stringency conditions,

(xxxiv) "SIMILAR TO SIDEROFLEXIN 4" (SEQ ID No:98) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SIMILAR TO SIDEROFLEXIN 4" encoded by a nucleic acid that hybridizes to the "SIMILAR TO SIDEROFLEXIN 4" nucleic acid or its complement under low stringency conditions,

(xxxv) "SPHINGOSINE KINASE 2" (SEQ ID No:99) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SPHINGOSINE KINASE 2" encoded by a nucleic acid that hybridizes to the "SPHINGOSINE KINASE 2" nucleic acid or its complement under low stringency conditions,

(xxxvi) "TRANSFERRIN RECEPTOR (P90, CD71)" (SEQ ID No:100) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TRANSFERRIN RECEPTOR (P90, CD71)" encoded by a nucleic acid that hybridizes to the "TRANSFERRIN RECEPTOR (P90, CD71)" nucleic acid or its complement under low stringency conditions,

(xxxvii) "TRANSFERRIN RECEPTOR PROTEIN 1 " (SEQ ID No:101) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TRANSFERRIN RECEPTOR PROTEIN 1 " encoded by a nucleic acid that hybridizes to the "TRANSFERRIN RECEPTOR PROTEIN 1" nucleic acid or its complement under low stringency conditions,

(xxxviii) "UV-DAMAGED DNA BINDING FACTOR" (SEQ ID No:102) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "UV-DAMAGED DNA BINDING FACTOR" encoded by a nucleic acid that hybridizes to the "UV-DAMAGED DNA BINDING FACTOR" nucleic acid or its complement under low stringency conditions,

(xxxix) "VAMP-ASSOCIATED PROTEIN B" (SEQ ID No:103) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "VAMP-ASSOCIATED PROTEIN B" encoded by a nucleic acid that hybridizes to the "VAMP-ASSOCIATED PROTEIN B" nucleic acid or its complement under low stringency conditions,

(xl) "VAV-3" (SEQ ID No:105) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "VAV-3" encoded by a nucleic acid that hybridizes to the "VAV-3" nucleic acid or its complement under low stringency conditions,

(xli) "WD-REPEAT PROTEIN 6" (SEQ ID No:106) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "WD-REPEAT PROTEIN 6" encoded by a nucleic acid that hybridizes to the "WD- REPEAT PROTEIN 6" nucleic acid or its complement under low stringency conditions, and

(xlii) "WUGSC:H_RG122E10.2A PROTEIN" (SEQ ID No:107) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "WUGSC:H_RG122E10.2A PROTEIN" encoded by a nucleic acid that hybridizes to the "WUGSC:H_RG122E10.2A PROTEIN" nucleic acid or its complement under low stringency conditions,

(xliii) "EGFR" (SEQ ID No:182) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "EGFR" encoded by a nucleic acid that hybridizes to the "EGFR" nucleic acid or its complement under low stringency conditions, and

(xliv) "Erbin" (SEQ ID No:183) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Erbin" encoded by a nucleic acid that hybridizes to the "Erbin" nucleic acid or its complement under low stringency conditions, and

(xlv) "GAP" (SEQ ID No:184) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "GAP" encoded by a nucleic acid that hybridizes to the "GAP" nucleic acid or its complement under low stringency conditions, and

(xlvi) "Grb7" (SEQ ID No:185) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Grb7" encoded by a nucleic acid that hybridizes to the "Grb7" nucleic acid or its complement under low stringency conditions, and

(xiv) "Her3" (SEQ ID No:186) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Her3" encoded by a nucleic acid that hybridizes to the "Her3" nucleic acid or its complement under low stringency conditions, and

(xv) "PLC gamma" (SEQ ID No:187) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PLC gamma" encoded by a nucleic acid that hybridizes to the "PLC gamma" nucleic acid or its complement under low stringency conditions, and and a complex (II) comprising at least two of said second proteins, wherein said low stringency conditions comprise hybridization in a buffer comprising 35% formamide, 5X

SSC, 50 mM Tris-HCI (pH 7.5), 5 mM EDTA, 0.02% PVP, 0.02% Ficoll, 0.2% BSA, 100 ug/ml denatured salmon sperm DNA, and 10% (wt/vol) dextran sulfate for 18-20 hours at

40 Celsius, washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4), 5 mM

EDTA, and 0.1 % SDS for 1.5 hours at 55 Celsius, and washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4), 5 mM EDTA, and 0.1% SDS for 1.5 hours at 60 Celsius.

2. The protein complex according to No. 1 wherein the first protein is the protein Her2 (SEQ ID NO. 84), or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of 'Her2' encoded by a nucleic acid that hybridizes to the 'Her2' under low stringency conditions.

(ii) "ANCIENT UBIQUITOUS PROTEIN 1 PRECURSOR" (SEQ ID No:59) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ANCIENT UBIQUITOUS PROTEIN 1 PRECURSOR" encoded by a nucleic acid that hybridizes to the "ANCIENT UBIQUITOUS PROTEIN 1 PRECURSOR" nucleic acid or its complement under low stringency conditions, (iii) "ATP-DEPENDENT METALLOPROTEASE FTSH1 HOMOLOG" (SEQ ID No:60) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ATP-DEPENDENT METALLOPROTEASE FTSH1 HOMOLOG" encoded by a nucleic acid that hybridizes to the "ATP-DEPENDENT METALLOPROTEASE FTSH1 HOMOLOG" nucleic acid or its complement under low stringency conditions,

(v) "CDC37 HOMOLOG" (SEQ ID No:62) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDC37 HOMOLOG" encoded by a nucleic acid that hybridizes to the "CDC37 HOMOLOG" nucleic acid or its complement under low stringency conditions,

(vii) "CDNA FLJ12681 FIS, CLONE NT2RM4002446" (SEQ ID No:64) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ 12681 FIS, CLONE NT2RM4002446" encoded by a nucleic acid that hybridizes to the "CDNA FLJ 12681 FIS, CLONE NT2RM4002446" nucleic acid or its complement under low stringency conditions,

(viii) "CDNA FLJ 13149 FIS, CLONE NT2RP3003344" (SEQ ID No:65) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ13149 FIS, CLONE NT2RP3003344" encoded by a nucleic acid that hybridizes to the "CDNA FLJ13149 FIS, CLONE NT2RP3003344" nucleic acid or its complement under low stringency conditions,

(ix) "CDNA FLJ13716 FIS, CLONE PLACE2000411 " (SEQ ID No:66) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ13716 FIS, CLONE PLACE2000411 " encoded by a nucleic acid that hybridizes to the "CDNA FLJ13716 FIS, CLONE PLACE2000411" nucleic acid or its complement under low stringency conditions,

(xi) "CDP-DIACYLGLYCEROL-INOSITOL 3-PHOSPHATIDYLTRANSFERASE" (SEQ ID

No:68) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDP-DIACYLGLYCEROL-INOSITOL 3-

PHOSPHATIDYLTRANSFERASE" encoded by a nucleic acid that hybridizes to the

"CDP-DIACYLGLYCEROL-INOSITOL 3-PHOSPHATIDYLTRANSFERASE" nucleic acid or its complement under low stringency conditions, (xii) "CHROMATIN-SPECIFIC TRANSCRIPTION ELONGATION FACTOR FACT 140 KDA SUBUNIT" (SEQ ID No:69) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CHROMATIN- SPECIFIC TRANSCRIPTION ELONGATION FACTOR FACT 140 KDA SUBUNIT" encoded by a nucleic acid that hybridizes to the "CHROMATIN-SPECIFIC TRANSCRIPTION ELONGATION FACTOR FACT 140 KDA SUBUNIT" nucleic acid or its complement under low stringency conditions,

(xvi) "Diacylglycerol kinase epsilon" (SEQ ID No:73) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Diacylglycerol kinase epsilon" encoded by a nucleic acid that hybridizes to the "Diacylglycerol kinase epsilon" nucleic acid or its complement under low stringency conditions,

(xvii) "EXCITATORY AMINO ACID TRANSPORTER 1 " (SEQ ID No:74) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "EXCITATORY AMINO ACID TRANSPORTER 1 " encoded by a nucleic acid that hybridizes to the "EXCITATORY AMINO ACID TRANSPORTER 1" nucleic acid or its complement under low stringency conditions,

(xx) "Grb2" (SEQ ID No:77) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Grb2" encoded by a nucleic acid that hybridizes to the "Grb2" nucleic acid or its complement under low stringency conditions,

(xxi) "HPT PROTEIN PRECURSOR" (SEQ ID No:78) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of

"HPT PROTEIN PRECURSOR" encoded by a nucleic acid that hybridizes to the "HPT

(xxii) "HSGCN1 (FRAGMENT)" (SEQ ID No:79) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of

"HSGCN1 (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "HSGCN1

(FRAGMENT)" nucleic acid or its complement under low stringency conditions,

(xxiii) "HYPOTHETICAL 35.7 KDA PROTEIN" (SEQ ID No:80) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYPOTHETICAL 35.7 KDA PROTEIN" encoded by a nucleic acid that hybridizes to the "HYPOTHETICAL 35.7 KDA PROTEIN" nucleic acid or its complement under low stringency conditions,

(xxiv) "HYPOTHETICAL 68.1 KDA PROTEIN" (SEQ ID No:81) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYPOTHETICAL 68.1 KDA PROTEIN" encoded by a nucleic acid that hybridizes to the "HYPOTHETICAL 68.1 KDA PROTEIN" nucleic acid or its complement under low stringency conditions,

(xxv) "HYPOTHETICAL PROTEIN XP_058906" (SEQ ID No:82) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYPOTHETICAL PROTEIN XP D58906" encoded by a nucleic acid that hybridizes to the "HYPOTHETICAL PROTEIN XP_058906" nucleic acid or its complement under low stringency conditions,

(xxvi) "Heat shock protein 90, alpha" (SEQ ID No:83) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of

(xxvii) "Her2" (SEQ ID No:84) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Her2" encoded by a nucleic acid that hybridizes to the "Her2" nucleic acid or its complement under low stringency conditions,

(xxviii) "Her4" (SEQ ID No:85) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Her4" encoded by a nucleic acid that hybridizes to the "Her4" nucleic acid or its complement under low stringency conditions,

(xxix) "INSULIN RECEPTOR SUBSTRATE 4" (SEQ ID No:86) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "INSULIN RECEPTOR SUBSTRATE 4" encoded by a nucleic acid that hybridizes to the "INSULIN RECEPTOR SUBSTRATE 4" nucleic acid or its complement under low stringency conditions,

(xxx) "KIAA0667 PROTEIN (FRAGMENT)" (SEQ ID No:87) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA0667 PROTEIN (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "KIAA0667 PROTEIN (FRAGMENT)" nucleic acid or its complement under low stringency conditions,

(xxxi) "KIAA0792 PROTEIN" (SEQ ID No:27) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA0792

(xxxii) "KIAA0887 PROTEIN (FRAGMENT)" (SEQ ID No:88) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA0887 PROTEIN (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "KIAA0887 PROTEIN (FRAGMENT)" nucleic acid or its complement under low stringency conditions, (xxxiii) "PALMITOYL-PROTEIN THIOESTERASE 1 PRECURSOR" (SEQ ID No:89) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PALMITOYL-PROTEIN THIOESTERASE 1 PRECURSOR" encoded by a nucleic acid that hybridizes to the "PALMITOYL-PROTEIN THIOESTERASE 1 PRECURSOR" nucleic acid or its complement under low stringency conditions,

(xxxiv) "PI3 kinase regulatory subunit p55 gamma" (SEQ ID No:90) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PI3 kinase regulatory subunit p55 gamma" encoded by a nucleic acid that hybridizes to the "Pl3 kinase regulatory subunit p55 gamma" nucleic acid or its complement under low stringency conditions,

(xxxv) "PI3 kinase regulatory subunit p85 alpha" (SEQ ID No:91) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PI3 kinase regulatory subunit p85 alpha" encoded by a nucleic acid that hybridizes to the "PI3 kinase regulatory subunit p85 alpha" nucleic acid or its complement under low stringency conditions,

(xxxvi) "PI3 kinase regulatory subunit p85 beta" (SEQ ID No:92) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PI3 kinase regulatory subunit p85 beta" encoded by a nucleic acid that hybridizes to the "PI3 kinase regulatory subunit p85 beta" nucleic acid or its complement under low stringency conditions,

(xxxvii) "PROCOLLAGEN-PROLINE, 2-OXOGLUTARATE 4-DIOXYGENASE (PROLINE 4- HYDROXYLASE), ALPHA POLYPEPTIDE I" (SEQ ID No:93) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PROCOLLAGEN-PROLINE, 2-OXOGLUTARATE 4-DIOXYGENASE (PROLINE 4- HYDROXYLASE), ALPHA POLYPEPTIDE I" encoded by a nucleic acid that hybridizes to the "PROCOLLAGEN-PROLINE, 2-OXOGLUTARATE 4- DIOXYGENASE (PROLINE 4- HYDROXYLASE), ALPHA POLYPEPTIDE I" nucleic acid or its complement under low stringency conditions,

(xxxviii) "RIBONUCLEOSIDE-DIPHOSPHATE REDUCTASE M2 CHAIN" (SEQ ID No:94) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "RIBONUCLEOSIDE-DIPHOSPHATE REDUCTASE M2 CHAIN" encoded by a nucleic acid that hybridizes to the "RIBONUCLEOSIDE-DIPHOSPHATE REDUCTASE M2 CHAIN" nucleic acid or its complement under low stringency conditions,

(xxxix) "SEL-1 HOMOLOG PRECURSOR" (SEQ ID No:95) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SEL-1 HOMOLOG PRECURSOR" encoded by a nucleic acid that hybridizes to the "SEL-1 HOMOLOG PRECURSOR" nucleic acid or its complement under low stringency conditions,

(xl) "SHC" (SEQ ID No:96) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SHC" encoded by a nucleic acid that hybridizes to the "SHC" nucleic acid or its complement under low stringency conditions,

(xli) "SIMILAR TO ADP.ATP CARRIER PROTEIN" (SEQ ID No:97) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SIMILAR TO ADP,ATP CARRIER PROTEIN" encoded by a nucleic acid that hybridizes to the "SIMILAR TO ADP.ATP CARRIER PROTEIN" nucleic acid or its complement under low stringency conditions,

(xlii) "SIMILAR TO SIDEROFLEXIN 4" (SEQ ID No:98) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of

"SIMILAR TO SIDEROFLEXIN 4" encoded by a nucleic acid that hybridizes to the

"SIMILAR TO SIDEROFLEXIN 4" nucleic acid or its complement under low stringency conditions,

(xliii) "SPHINGOSINE KINASE 2" (SEQ ID No:99) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of

"SPHINGOSINE KINASE 2" encoded by a nucleic acid that hybridizes to the

"SPHINGOSINE KINASE 2" nucleic acid or its complement under low stringency conditions,

(xliv) "TRANSFERRIN RECEPTOR (P90, CD71)" (SEQ ID No:100) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TRANSFERRIN RECEPTOR (P90, CD71)" encoded by a nucleic acid that hybridizes to the "TRANSFERRIN RECEPTOR (P90, CD71)" nucleic acid or its complement under low stringency conditions,

(xlv) "TRANSFERRIN RECEPTOR PROTEIN 1 " (SEQ ID No:101) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TRANSFERRIN RECEPTOR PROTEIN 1 " encoded by a nucleic acid that hybridizes to the "TRANSFERRIN RECEPTOR PROTEIN 1 " nucleic acid or its complement under low stringency conditions,

(xlvi) "UV-DAMAGED DNA BINDING FACTOR" (SEQ ID No:102) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "UV-DAMAGED DNA BINDING FACTOR" encoded by a nucleic acid that hybridizes to the "UV-DAMAGED DNA BINDING FACTOR" nucleic acid or its complement under low stringency conditions,

(xlvii) "VAMP-ASSOCIATED PROTEIN B" (SEQ ID No:103) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "VAMP-ASSOCIATED PROTEIN B" encoded by a nucleic acid that hybridizes to the "VAMP-ASSOCIATED PROTEIN B" nucleic acid or its complement under low stringency conditions,

(xlviii) "VAV-2" (SEQ ID No:104) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "VAV-2" encoded by a nucleic acid that hybridizes to the "VAV-2" nucleic acid or its complement under low stringency conditions,

(xlix) "VAV-3" (SEQ ID No:105) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "VAV-3" encoded by a nucleic acid that hybridizes to the "VAV-3" nucleic acid or its complement under low stringency conditions,

(I) "WD-REPEAT PROTEIN 6" (SEQ ID No:106) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "WD-REPEAT PROTEIN 6" encoded by a nucleic acid that hybridizes to the "WD- REPEAT PROTEIN 6" nucleic acid or its complement under low stringency conditions, and

(Ii) "WUGSC:H_RG122E10.2A PROTEIN" (SEQ ID No:107) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "WUGSC:H_RG122E10.2A PROTEIN" encoded by a nucleic acid that hybridizes to the "WUGSC:H_RG122E10.2A PROTEIN" nucleic acid or its complement under low stringency conditions,

(Iii) "EGFR" (SEQ ID No:182) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "EGFR" encoded by a nucleic acid that hybridizes to the "EGFR" nucleic acid or its complement under low stringency conditions, and (liii) "Erbin" (SEQ ID No:183) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Erbin" encoded by a nucleic acid that hybridizes to the "Erbin" nucleic acid or its complement under low stringency conditions, and

(liv) "GAP" (SEQ ID No:184) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "GAP" encoded by a nucleic acid that hybridizes to the "GAP" nucleic acid or its complement under low stringency conditions, and

(Iv) "Grb7" (SEQ ID No:185) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Grb7" encoded by a nucleic acid that hybridizes to the "Grb7" nucleic acid or its complement under low stringency conditions, and

(Ivi) "Her3" (SEQ ID No:186) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Her3" encoded by a nucleic acid that hybridizes to the "Her3" nucleic acid or its complement under low stringency conditions, and

(Ivii) "PLC gamma" (SEQ ID No:187) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PLC gamma" encoded by a nucleic acid that hybridizes to the "PLC gamma" nucleic acid or its complement under low stringency conditions, and a protein complex selected from complex (II) and comprising the following proteins: (i) "ALZHEIMER'S DISEASE AMYLOID A4 PROTEIN PRECURSOR" (SEQ ID No:58) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ALZHEIMER'S DISEASE AMYLOID A4 PROTEIN PRECURSOR" encoded by a nucleic acid that hybridizes to the "ALZHEIMER'S DISEASE AMYLOID A4 PROTEIN PRECURSOR" nucleic acid or its complement under low stringency conditions,

HOMOLOG" encoded by a nucleic acid that hybridizes to the "ATP-DEPENDENT

(viii) "CDNA FLJ13149 FIS, CLONE NT2RP3003344" (SEQ ID No:65) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ 13149 FIS, CLONE NT2RP3003344" encoded by a nucleic acid that hybridizes to the "CDNA FLJ13149 FIS, CLONE NT2RP3003344" nucleic acid or its complement under low stringency conditions,

(ix) "CDNA FLJ13716 FIS, CLONE PLACE2000411 " (SEQ ID No:66) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ13716 FIS, CLONE PLACE2000411 " encoded by a nucleic acid that hybridizes to the "CDNA FLJ13716 FIS, CLONE PLACE2000411 " nucleic acid or its complement under low stringency conditions, (x) "CDNA: FLJ22087 FIS, CLONE HEP15918" (SEQ ID No:67) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA: FLJ22087 FIS, CLONE HEP15918" encoded by a nucleic acid that hybridizes to the "CDNA: FLJ22087 FIS, CLONE HEP15918" nucleic acid or its complement under low stringency conditions,

(xii) "CHROMATIN-SPECIFIC TRANSCRIPTION ELONGATION FACTOR FACT 140 KDA SUBUNIT" (SEQ ID No:69) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CHROMATIN- SPECIFIC TRANSCRIPTION ELONGATION FACTOR FACT 140 KDA SUBUNIT" encoded by a nucleic acid that hybridizes to the "CHROMATIN-SPECIFIC TRANSCRIPTION ELONGATION FACTOR FACT 140 KDA SUBUNIT" nucleic acid or its complement under low stringency conditions,

(xiii) "COLLAPSIN RESPONSE MEDIATOR PROTEIN-5" (SEQ ID No:70) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "COLLAPSIN RESPONSE MEDIATOR PROTEIN-5" encoded by a nucleic acid that hybridizes to the "COLLAPSIN RESPONSE MEDIATOR PROTEIN-5" nucleic acid or its complement under low stringency conditions, (xiv) "DIHYDROPYRIMIDINASE RELATED PROTEIN-5" (SEQ ID No:71) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "DIHYDROPYRIMIDINASE RELATED PROTEIN-5" encoded by a nucleic acid that hybridizes to the "DIHYDROPYRIMIDINASE RELATED PROTEIN-5" nucleic acid or its complement under low stringency conditions, (xv) "DOPAMINE-RESPONSIVE PROTEIN" (SEQ ID No:72) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "DOPAMINE-RESPONSIVE PROTEIN" encoded by a nucleic acid that hybridizes to the "DOPAMINE-RESPONSIVE PROTEIN" nucleic acid or its complement under low stringency conditions, (xvi) "Diacylglycerol kinase epsilon" (SEQ ID No:73) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of

(xvii) "EXCITATORY AMINO ACID TRANSPORTER 1" (SEQ ID No:74) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "EXCITATORY AMINO ACID TRANSPORTER 1" encoded by a nucleic acid that hybridizes to the "EXCITATORY AMINO ACID TRANSPORTER 1" nucleic acid or its complement under low stringency conditions,

"HPT PROTEIN PRECURSOR" encoded by a nucleic acid that hybridizes to the "HPT

"HSGCN1 (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "HSGCN1

(FRAGMENT)" nucleic acid or its complement under low stringency conditions,

(xxv) "HYPOTHETICAL PROTEIN XP_058906" (SEQ ID No:82) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYPOTHETICAL PROTEIN XP_058906" encoded by a nucleic acid that hybridizes to the "HYPOTHETICAL PROTEIN XP_058906" nucleic acid or its complement under low stringency conditions,

(xxxii) "KIAA0887 PROTEIN (FRAGMENT)" (SEQ ID No:88) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA0887 PROTEIN (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "KIAA0887 PROTEIN (FRAGMENT)" nucleic acid or its complement under low stringency conditions,

(xxxiii) "PALMITOYL-PROTEIN THIOESTERASE 1 PRECURSOR" (SEQ ID No:89) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PALMITOYL-PROTEIN THIOESTERASE 1

PRECURSOR" encoded by a nucleic acid that hybridizes to the "PALMITOYL-PROTEIN

THIOESTERASE 1 PRECURSOR" nucleic acid or its complement under low stringency conditions,

(xxxiv) "PI3 kinase regulatory subunit p55 gamma" (SEQ ID No:90) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PI3 kinase regulatory subunit p55 gamma" encoded by a nucleic acid that hybridizes to the "PI3 kinase regulatory subunit p55 gamma" nucleic acid or its complement under low stringency conditions,

(xxxvii) "PROCOLLAGEN-PROLINE, 2-OXOGLUTARATE 4-DIOXYGENASE (PROLINE

4- HYDROXYLASE), ALPHA POLYPEPTIDE I" (SEQ ID No:93) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PROCOLLAGEN-PROLINE, 2-OXOGLUTARATE 4-DIOXYGENASE

(PROLINE 4- HYDROXYLASE), ALPHA POLYPEPTIDE l" encoded by a nucleic acid that hybridizes to the "PROCOLLAGEN-PROLINE, 2-OXOGLUTARATE 4-

DIOXYGENASE (PROLINE 4- HYDROXYLASE), ALPHA POLYPEPTIDE I" nucleic acid or its complement under low stringency conditions,

(xxxviii) "RIBONUCLEOSIDE-DIPHOSPHATE REDUCTASE M2 CHAIN" (SEQ ID

No:94) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "RIBONUCLEOSIDE-DIPHOSPHATE

REDUCTASE M2 CHAIN" encoded by a nucleic acid that hybridizes to the

"RIBONUCLEOSIDE-DIPHOSPHATE REDUCTASE M2 CHAIN" nucleic acid or its complement under low stringency conditions,

(xii) "SIMILAR TO ADP.ATP CARRIER PROTEIN" (SEQ ID No:97) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SIMILAR TO ADP.ATP CARRIER PROTEIN" encoded by a nucleic acid that hybridizes to the "SIMILAR TO ADP.ATP CARRIER PROTEIN" nucleic acid or its complement under low stringency conditions,

"SIMILAR TO SIDEROFLEXIN 4" encoded by a nucleic acid that hybridizes to the

"SPHINGOSINE KINASE 2" encoded by a nucleic acid that hybridizes to the "SPHINGOSINE KINASE 2" nucleic acid or its complement under low stringency conditions,

(xlv) "TRANSFERRIN RECEPTOR PROTEIN 1 " (SEQ ID No: 101) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TRANSFERRIN RECEPTOR PROTEIN 1 " encoded by a nucleic acid that hybridizes to the "TRANSFERRIN RECEPTOR PROTEIN 1 " nucleic acid or its complement under low stringency conditions,

(I) "WD-REPEAT PROTEIN 6" (SEQ ID No:106) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of

"WD-REPEAT PROTEIN 6" encoded by a nucleic acid that hybridizes to the "WD- REPEAT PROTEIN 6" nucleic acid or its complement under low stringency conditions, and

(Ii) "WUGSC:H_RG122E10.2A PROTEIN" (SEQ ID No:107) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "WUGSC:H_RG122E10.2A PROTEIN" encoded by a nucleic acid that hybridizes to the "WUGSC:H_RG122E10.2A PROTEIN" nucleic acid or its complement under low stringency conditions, and a protein complex selected from complex (III) and comprising the following proteins:

(ii) "CDC37 HOMOLOG" (SEQ ID No:62) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDC37 HOMOLOG" encoded by a nucleic acid that hybridizes to the "CDC37 HOMOLOG" nucleic acid or its complement under low stringency conditions,

(iii) "CHROMATIN-SPECIFIC TRANSCRIPTION ELONGATION FACTOR FACT 140 KDA SUBUNIT" (SEQ ID No:69) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CHROMATIN- SPECIFIC TRANSCRIPTION ELONGATION FACTOR FACT 140 KDA SUBUNIT" encoded by a nucleic acid that hybridizes to the "CHROMATIN-SPECIFIC TRANSCRIPTION ELONGATION FACTOR FACT 140 KDA SUBUNIT" nucleic acid or its complement under low stringency conditions,

(iv) "Diacylglycerol kinase epsilon" (SEQ ID No:73) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Diacylglycerol kinase epsilon" encoded by a nucleic acid that hybridizes to the "Diacylglycerol kinase epsilon" nucleic acid or its complement under low stringency conditions,

(v) "FILAMIN A" (SEQ ID No:75) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "FILAMIN A" encoded by a nucleic acid that hybridizes to the "FILAMIN A" nucleic acid or its complement under low stringency conditions, (vi) "Grb2" (SEQ ID No:77) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Grb2" encoded by a nucleic acid that hybridizes to the "Grb2" nucleic acid or its complement under low stringency conditions,

(vii) "HYPOTHETICAL 35.7 KDA PROTEIN" (SEQ ID No:80) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYPOTHETICAL 35.7 KDA PROTEIN" encoded by a nucleic acid that hybridizes to the "HYPOTHETICAL 35.7 KDA PROTEIN" nucleic acid or its complement under low stringency conditions,

(viii) "HYPOTHETICAL 68.1 KDA PROTEIN" (SEQ ID No:81) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYPOTHETICAL 68.1 KDA PROTEIN" encoded by a nucleic acid that hybridizes to the "HYPOTHETICAL 68.1 KDA PROTEIN" nucleic acid or its complement under low stringency conditions,

(ix) "Heat shock protein 90, alpha" (SEQ ID No:83) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Heat shock protein 90, alpha" encoded by a nucleic acid that hybridizes to the "Heat shock protein 90, alpha" nucleic acid or its complement under low stringency conditions, (x) "Her2" (SEQ ID No:84) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Her2" encoded by a nucleic acid that hybridizes to the "Her2" nucleic acid or its complement under low stringency conditions,

(xi) "Her4" (SEQ ID No:85) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Her4" encoded by a nucleic acid that hybridizes to the "Her4" nucleic acid or its complement under low stringency conditions,

(xii) "INSULIN RECEPTOR SUBSTRATE 4" (SEQ ID No:86) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "INSULIN RECEPTOR SUBSTRATE 4" encoded by a nucleic acid that hybridizes to the "INSULIN RECEPTOR SUBSTRATE 4" nucleic acid or its complement under low stringency conditions,

(xiii) "PI3 kinase regulatory subunit p55 gamma" (SEQ ID No:90) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog. thereof, or a., variant of "PI3 kinase regulatory subunit p55 gamma" encoded by a nucleic acid that hybridizes to the "PI3 kinase regulatory subunit p55 gamma" nucleic acid or its complement under low stringency conditions,

(xiv) "PI3 kinase regulatory subunit p85 alpha" (SEQ ID No:91) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PI3 kinase regulatory subunit p85 alpha" encoded by a nucleic acid that hybridizes to the "PI3 kinase regulatory subunit p85 alpha" nucleic acid or its complement under low stringency conditions,

(xv) "PI3 kinase regulatory subunit p85 beta" (SEQ ID No:92) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PI3 kinase regulatory subunit p85 beta" encoded by a nucleic acid that hybridizes to the "PI3 kinase regulatory subunit p85 beta" nucleic acid or its complement under low stringency conditions,

(xvi) "SEL-1 HOMOLOG PRECURSOR" (SEQ ID No:95) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SEL-1 HOMOLOG PRECURSOR" encoded by a nucleic acid that hybridizes to the "SEL-1 HOMOLOG PRECURSOR" nucleic acid or its complement under low stringency conditions,

(xvii) "SHC" (SEQ ID No:96) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SHC" encoded by a nucleic acid that hybridizes to the "SHC" nucleic acid or its complement under low stringency conditions,

(xviii) "SPHINGOSINE KINASE 2" (SEQ ID No:99) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SPHINGOSINE KINASE 2" encoded by a nucleic acid that hybridizes to the "SPHINGOSINE KINASE 2" nucleic acid or its complement under low stringency conditions,

(xix) "VAV-2" (SEQ ID No:104) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "VAV-2" encoded by a nucleic acid that hybridizes to the "VAV-2" nucleic acid or its complement under low stringency conditions,

(xx) "VAV-3" (SEQ ID No:105) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "VAV-3" encoded by a nucleic acid that hybridizes to the "VAV-3" nucleic acid or its complement under low stringency conditions, (xxi) "WD-REPEAT PROTEIN 6" (SEQ ID No:106) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "WD-REPEAT PROTEIN 6" encoded by a nucleic acid that hybridizes to the "WD- REPEAT PROTEIN 6" nucleic acid or its complement under low stringency conditions.

4. The protein complex according to No. 1 comprising all but 1 - 47 of the following proteins:

(i) "ALZHEIMER'S DISEASE AMYLOID A4 PROTEIN PRECURSOR" (SEQ ID No:58) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ALZHEIMER'S DISEASE AMYLOID A4 PROTEIN

PRECURSOR" encoded by a nucleic acid that hybridizes to the "ALZHEIMER'S

DISEASE AMYLOID A4 PROTEIN PRECURSOR" nucleic acid or its complement under low stringency conditions,

(ii) "ANCIENT UBIQUITOUS PROTEIN 1 PRECURSOR" (SEQ ID No:59) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ANCIENT UBIQUITOUS PROTEIN 1 PRECURSOR" encoded by a nucleic acid that hybridizes to the "ANCIENT UBIQUITOUS PROTEIN 1

PRECURSOR" nucleic acid or its complement under low stringency conditions,

(iii) "ATP-DEPENDENT METALLOPROTEASE FTSH1 HOMOLOG" (SEQ ID No:60) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ATP-DEPENDENT METALLOPROTEASE FTSH1

HOMOLOG" encoded by a nucleic acid that hybridizes to the "ATP-DEPENDENT

HOMOLOG" encoded by a nucleic acid that hybridizes to the "CDC37 HOMOLOG" nucleic acid or its complement under low stringency conditions, (vi) "CDNA FLJ12443 FIS, CLONE NT2RM1000186" (SEQ ID No:63) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ12443 FIS, CLONE NT2RM1000186" encoded by a nucleic acid that hybridizes to the "CDNA FLJ12443 FIS, CLONE NT2RM1000186" nucleic acid or its complement under low stringency conditions,

(xii) "CHROMATIN-SPECIFIC TRANSCRIPTION ELONGATION FACTOR FACT 140 KDA SUBUNIT" (SEQ ID No:69) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CHROMATIN- SPECIFIC TRANSCRIPTION ELONGATION FACTOR FACT 140 KDA SUBUNIT" encoded by a nucleic acid that hybridizes to the "CHROMATIN-SPECIFIC

TRANSCRIPTION ELONGATION FACTOR FACT 140 KDA SUBUNIT" nucleic acid or its complement under low stringency conditions,

(xiii) "COLLAPSIN RESPONSE MEDIATOR PROTEIN-5" (SEQ ID No:70) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "COLLAPSIN RESPONSE MEDIATOR PROTEIN-5" encoded by a nucleic acid that hybridizes to the "COLLAPSIN RESPONSE MEDIATOR

PROTEIN-5" nucleic acid or its complement under low stringency conditions,

(xiv) "DIHYDROPYRIMIDINASE RELATED PROTEIN-5" (SEQ ID No:71) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "DIHYDROPYRIMIDINASE RELATED PROTEIN-5" encoded by a nucleic acid that hybridizes to the "DIHYDROPYRIMIDINASE RELATED

PROTEIN-5" nucleic acid or its complement under low stringency conditions,

(xv) "DOPAMINE-RESPONSIVE PROTEIN" (SEQ ID No:72) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "DOPAMINE-RESPONSIVE PROTEIN" encoded by a nucleic acid that hybridizes to the "DOPAMINE-RESPONSIVE PROTEIN" nucleic acid or its complement under low stringency conditions,

(xviii) "FILAMIN A" (SEQ ID No:75) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "FILAMIN A" encoded by a nucleic acid that hybridizes to the "FILAMIN A" nucleic acid or its complement under low stringency conditions, (xix) "GPI8 PROTEIN (FRAGMENT)" (SEQ ID No:76) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of

"HPT PROTEIN PRECURSOR" encoded by a nucleic acid that hybridizes to the "HPT

"HSGCN1 (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "HSGCN1

(FRAGMENT)" nucleic acid or its complement under low stringency conditions,

(xxv) "HYPOTHETICAL PROTEIN XP_058906" (SEQ ID No:82) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYPOTHETICAL PROTEIN XP_058906" encoded by a nucleic acid that hybridizes to the "HYPOTHETICAL PROTEIN XP_058906" nucleic acid or its complement under low stringency conditions, (xxvi) "Heat shock protein 90, alpha" (SEQ ID No:83) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of

(xxxiii) "PALMITOYL-PROTEIN THIOESTERASE 1 PRECURSOR" (SEQ ID No:89) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PALMITOYL-PROTEIN THIOESTERASE 1 PRECURSOR" encoded by a nucleic acid that hybridizes to the "PALMITOYL-PROTEIN

(xxxvi) "PI3 kinase regulatory subunit ρ85 beta" (SEQ ID No:92) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PI3 kinase regulatory subunit p85 beta" encoded by a nucleic acid that hybridizes to the "PI3 kinase regulatory subunit p85 beta" nucleic acid or its complement under low stringency conditions,

(xxxvii) "PROCOLLAGEN-PROLINE, 2-OXOGLUTARATE 4-DIOXYGENASE (PROLINE

(PROLINE 4- HYDROXYLASE), ALPHA POLYPEPTIDE I" encoded by a nucleic acid that hybridizes to the "PROCOLLAGEN-PROLINE, 2-OXOGLUTARATE 4-

(xxxviii) "RIBONUCLEOSIDE-DIPHOSPHATE REDUCTASE M2 CHAIN" (SEQ ID

REDUCTASE M2 CHAIN" encoded by a nucleic acid that hybridizes to the

"SIMILAR TO SIDEROFLEXIN 4" encoded by a nucleic acid that hybridizes to the

"SPHINGOSINE KINASE 2" encoded by a nucleic acid that hybridizes to the

(xlv) "TRANSFERRIN RECEPTOR PROTEIN 1 " (SEQ ID No:101) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TRANSFERRIN RECEPTOR PROTEIN 1 " encoded by a nucleic acid that hybridizes to the "TRANSFERRIN RECEPTOR PROTEIN 1" nucleic acid or its complement under low stringency conditions,

(xlvi) "UV-DAMAGED DNA BINDING FACTOR" (SEQ ID No: 102) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "UV-DAMAGED DNA BINDING FACTOR" encoded by a nucleic acid that hybridizes to the "UV-DAMAGED DNA BINDING FACTOR" nucleic acid or its complement under low stringency conditions,

(I) "WD-REPEAT PROTEIN 6" (SEQ ID No:106) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "WD-REPEAT PROTEIN 6" encoded by a nucleic acid that hybridizes to the "WD- REPEAT PROTEIN 6" nucleic acid or its complement under low stringency conditions, (Ii) "WUGSC:H_RG122E10.2A PROTEIN" (SEQ ID No:107) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "WUGSC:H_RG122E10.2A PROTEIN" encoded by a nucleic acid that hybridizes to the "WUGSC:H_RG122E10.2A PROTEIN" nucleic acid or its complement under low stringency conditions,.

(Iii) "EGFR" (SEQ ID No:182) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "EGFR" encoded by a nucleic acid that hybridizes to the "EGFR" nucleic acid or its complement under low stringency conditions, and

(liii) "Erbin" (SEQ ID No:183) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Erbin" encoded by a nucleic acid that hybridizes to the "Erbin" nucleic acid or its complement under low stringency conditions, and (liv) "GAP" (SEQ ID No:184) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "GAP" encoded by a nucleic acid that hybridizes to the "GAP" nucleic acid or its complement under low stringency conditions, and

(Ivii) "PLC gamma" (SEQ ID No:187) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PLC gamma" encoded by a nucleic acid that hybridizes to the "PLC gamma" nucleic acid or its complement under low stringency conditions

8. The complex of any of No. 1 - 7 that is involved in the kinase activity, diacylglycerol kinase activity or sphingosine kinase activity. 9. A process for preparing a complex of any of No. 1 - 8 and optionally the components thereof comprising the following steps:expressing a protein (bait) of the complex, preferably a tagged protein, in a target cell, isolating the protein complex which is attached to the bait protein, and optionally dissociating the protein complex and isolating the individual complex members.

12. Component of the Her2 complex obtainable by a process according to any of No. 9 - 11.

13. Protein of the Her2 complex selected from

(i) "CDNA FLJ12443 FIS, CLONE NT2RM1000186" (SEQ ID No:63) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ12443 FIS, CLONE NT2RM1000186" encoded by a nucleic acid that hybridizes to the "CDNA FLJ12443 FIS, CLONE NT2RM1000186" nucleic acid or its complement under low stringency conditions,

(ii) "CDNA FLJ12681 FIS, CLONE NT2RM4002446" (SEQ ID No:64) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ 12681 FIS, CLONE NT2RM4002446" encoded by a nucleic acid that hybridizes to the "CDNA FLJ 12681 FIS, CLONE NT2RM4002446" nucleic acid or its complement under low stringency conditions,

(iii) "CDNA FLJ13149 FIS, CLONE NT2RP3003344" (SEQ ID No:65) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ 13149 FIS, CLONE NT2RP3003344" encoded by a nucleic acid that hybridizes to the "CDNA FLJ13149 FIS, CLONE NT2RP3003344" nucleic acid or its complement under low stringency conditions,

(iv) "CDNA FLJ13716 FIS, CLONE PLACE2000411 " (SEQ ID No:66) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ13716 FIS, CLONE PLACE2000411 " encoded by a nucleic acid that hybridizes to the "CDNA FLJ13716 FIS, CLONE PLACE2000411 " nucleic acid or its complement under low stringency conditions,

(v) "CDNA: FLJ22087 FIS, CLONE HEP15918" (SEQ ID No:67) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA: FLJ22087 FIS, CLONE HEP15918" encoded by a nucleic acid that hybridizes to the "CDNA: FLJ22087 FIS, CLONE HEP15918" nucleic acid or its complement under low stringency conditions,

(vi) "HSGCN1 (FRAGMENT)" (SEQ ID No:79) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HSGCN1

(FRAGMENT)" encoded by a nucleic acid that hybridizes to the "HSGCN1

(FRAGMENT)" nucleic acid or its complement under low stringency conditions,

(ix) "HYPOTHETICAL PROTEIN XPJ 58906" (SEQ ID No:82) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYPOTHETICAL PROTEIN XP_058906" encoded by a nucleic acid that hybridizes to the "HYPOTHETICAL PROTEIN XP_058906" nucleic acid or its complement under low stringency conditions,

(x) "KIAA0667 PROTEIN (FRAGMENT)" (SEQ ID No:87) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA0667 PROTEIN (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "KIAA0667 PROTEIN (FRAGMENT)" nucleic acid or its complement under low stringency conditions,

(xi) "K1AA0792 PROTEIN" (SEQ ID No:27) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA0792 250

nucleic acid that hybridizes to the "cdk2" nucleic acid or its complement under low stringency conditions.

8. The complex of any of No. 1 - 7 that is involved in the kinase activation.

12. Component of the Ringo 1 complex obtainable by a process according to any of No. 9 - 11. 201

(xii) "KIAA0887 PROTEIN (FRAGMENT)" (SEQ ID No:88) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA0887 PROTEIN (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "K1AA0887 PROTEIN (FRAGMENT)" nucleic acid or its complement under low stringency conditions,

(xiii) "SIMILAR TO SIDEROFLEXIN 4" (SEQ ID No:98) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SIMILAR TO SIDEROFLEXIN 4" encoded by a nucleic acid that hybridizes to the "SIMILAR TO SIDEROFLEXIN 4" nucleic acid or its complement under low stringency conditions,

(xiv) "WD-REPEAT PROTEIN 6" (SEQ ID No:106) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "WD-REPEAT PROTEIN 6" encoded by a nucleic acid that hybridizes to the "WD- REPEAT PROTEIN 6" nucleic acid or its complement under low stringency conditions, and

(xv) "WUGSC:H_RG122E10.2A PROTEIN" (SEQ ID No:107) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "WUGSC:H_RG122E10.2A PROTEIN" encoded by a nucleic acid that hybridizes to the "WUGSC:H_RG122E10.2A PROTEIN" nucleic acid or its complement under low stringency conditions, wherein said low stringency conditions comprise hybridization in a buffer comprising 35% formamide, 5X SSC, 50 mM Tris-HCI (pH 7.5), 5 mM EDTA, 0.02% PVP, 0.02% Ficoll, 0.2% BSA, 100 ug/ml denatured salmon sperm DNA, and 10% (wt/vol) dextran sulfate for 18-20 hours at 40 Celsius, washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4), 5 mM EDTA, and 0.1 % SDS for 1.5 hours at 55 Celsius, and washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4), 5 mM EDTA, and 0.1% SDS for 1.5 hours at 60 Celsius.

14. Nucleic acid encoding a protein according to No. 13.

15. Construct, preferably a vector construct, comprising (a) a nucleic acid according to No. 14 and at least one further nucleic acid which is normally not associated with said nucleic acid, or 202

19. The kit according to No. 18 for processing a substrate of said complex.

20. The kit according to No. 18 for the diagnosis or prognosis of a disease or a disease risk, preferentially for a disease or disorder such as cancer such as breast cancer, ovarian cancer, lung cancer, stomach cancer, bladder cancer. 203

(ii) "CDNA FLJ12681 FIS, CLONE NT2RM4002446" (SEQ ID No:64) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ 12681 FIS, CLONE NT2RM4002446" encoded by a nucleic acid that hybridizes to the "CDNA FLJ12681 FIS, CLONE NT2RM4002446" nucleic acid or its complement under low stringency conditions,

(iii) "CDNA FLJ13149 FIS, CLONE NT2RP3003344" (SEQ ID No:65) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ13149 FIS, CLONE NT2RP3003344" encoded by a nucleic acid that hybridizes to the "CDNA FLJ13149 FIS, CLONE NT2RP3003344" nucleic acid or its complement under low stringency conditions,

(iv) "CDNA FLJ13716 FIS, CLONE PLACE2000411" (SEQ ID No:66) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ13716 FIS, CLONE PLACE2000411 " encoded by a nucleic acid that hybridizes to the "CDNA FLJ13716 FIS, CLONE PLACE2000411 " nucleic acid or its complement under low stringency conditions,

(v) "CDNA: FLJ22087 FIS, CLONE HEP15918" (SEQ ID No:67) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA: FLJ22087 FIS, CLONE HEP15918" encoded by a nucleic acid that 204

hybridizes to the "CDNA: FLJ22087 FIS, CLONE HEP15918" nucleic acid or its complement under low stringency conditions,

(FRAGMENT)" encoded by a nucleic acid that hybridizes to the "HSGCN1

(FRAGMENT)" nucleic acid or its complement under low stringency conditions,

(ix) "HYPOTHETICAL PROTEIN XP_058906" (SEQ ID No:82) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYPOTHETICAL PROTEIN XP_058906" encoded by a nucleic acid that hybridizes to the "HYPOTHETICAL PROTEIN XP_058906" nucleic acid or its complement under low stringency conditions,

(xi) "KIAA0792 PROTEIN" (SEQ ID No:27) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA0792

(xii) "KIAA0887 PROTEIN (FRAGMENT)" (SEQ ID No:88) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA0887 PROTEIN (FRAGMENT)" encoded by a nucleic acid that hybridizes 205

to the "KIAA0887 PROTEIN (FRAGMENT)" nucleic acid or its complement under low stringency conditions,

(xiv) "WD-REPEAT PROTEIN 6" (SEQ ID No:106) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "WD-REPEAT PROTEIN 6" encoded by a nucleic acid that hybridizes to the "WD- REPEAT PROTEIN 6" nucleic acid or its complement under low stringency conditions, and/or

(xv) "WUGSC:H_RG122E10.2A PROTEIN" (SEQ ID No:107) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "WUGSC:H_RG122E10.2A PROTEIN" encoded by a nucleic acid that hybridizes to the "WUGSC:H_RG122E10.2A PROTEIN" nucleic acid or its complement under low stringency conditions, and a pharmaceutical acceptable carrier.

24. A pharmaceutical composition according to No. 23 for the treatment of diseases and disorders such as cancer such as breast cancer, ovarian cancer, lung cancer, stomach cancer, bladder cancer.

(ii) "CDNA FLJ12681 FIS, CLONE NT2RM4002446" (SEQ ID No:64) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ12681 FIS, CLONE NT2RM4002446" encoded by a nucleic 206

acid that hybridizes to the "CDNA FLJ12681 FIS, CLONE NT2RM4002446" nucleic acid or its complement under low stringency conditions,

(FRAGMENT)" encoded by a nucleic acid that hybridizes to the "HSGCN1

(FRAGMENT)" nucleic acid or its complement under low stringency conditions,

(ix) "HYPOTHETICAL PROTEIN XP_058906" (SEQ ID No:82) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYPOTHETICAL PROTEIN XP_058906" encoded by a nucleic acid that 207

hybridizes to the "HYPOTHETICAL PROTEIN XP_058906" nucleic acid or its complement under low stringency conditions,

(xi) "KIAA0792 PROTEIN" (SEQ ID No:27) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA0792 PROTEIN" encoded by a nucleic acid that hybridizes to the "K1AA0792 PROTEIN" nucleic acid or its complement under low stringency conditions,

(xii) "KIAA0887 PROTEIN (FRAGMENT)" (SEQ ID No:88) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA0887 PROTEIN (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "KIAA0887 PROTEIN (FRAGMENT)" nucleic acid or its complement under low stringency conditions,

(xv) "WUGSC:H_RG122E10.2A PROTEIN" (SEQ ID No:107) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "WUGSC:H_RG122E10.2A PROTEIN" encoded by a nucleic acid that hybridizes to the "WUGSC:H_RG122E10.2A PROTEIN" nucleic acid or its complement under low stringency conditions, comprising the steps of

(b) determinig whether said candidate molecule is bound to the complex or protein. 208

26. A method for screening for a molecule that modulates directly or indirectly the function, activity, composition or formation of the complex of any one of No. 1 - 8 comprising the steps of(a) exposing said complex, or a cell or organism containing Her2 complex to one or more candidate molecules; and

27. The method of No. 26, wherein the amount of said complex is determined.

28. The method of No. 26, wherein the activity of said complex is determined.

31. The method of No. 30, wherein said determining step comprises determining whether (i) "ALZHEIMER'S DISEASE AMYLOID A4 PROTEIN PRECURSOR" (SEQ ID No:58) or a functionally active derivative thereof, or a functionally active fragment thereof, or a 209

homolog thereof, or a variant of "ALZHEIMER'S DISEASE AMYLOID A4 PROTEIN PRECURSOR" encoded by a nucleic acid that hybridizes to the "ALZHEIMER'S DISEASE AMYLOID A4 PROTEIN PRECURSOR" nucleic acid or its complement under low stringency conditions, and/or

(ii) "ANCIENT UBIQUITOUS PROTEIN 1 PRECURSOR" (SEQ ID No:59) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ANCIENT UBIQUITOUS PROTEIN 1 PRECURSOR" encoded by a nucleic acid that hybridizes to the "ANCIENT UBIQUITOUS PROTEIN 1 PRECURSOR" nucleic acid or its complement under low stringency conditions, and/or (iii) "ATP-DEPENDENT METALLOPROTEASE FTSH1 HOMOLOG" (SEQ ID No:60) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ATP-DEPENDENT METALLOPROTEASE FTSH1 HOMOLOG" encoded by a nucleic acid that hybridizes to the "ATP-DEPENDENT METALLOPROTEASE FTSH1 HOMOLOG" nucleic acid or its complement under low stringency conditions, and/or

(iv) "B-CELL RECEPTOR ASSOCIATED PROTEIN" (SEQ ID No:61) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "B-CELL RECEPTOR ASSOCIATED PROTEIN" encoded by a nucleic acid that hybridizes to the "B-CELL RECEPTOR ASSOCIATED PROTEIN" nucleic acid or its complement under low stringency conditions, and/or

(v) "CDC37 HOMOLOG" (SEQ ID No:62) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDC37 HOMOLOG" encoded by a nucleic acid that hybridizes to the "CDC37 HOMOLOG" nucleic acid or its complement under low stringency conditions, and/or (vi) "CDNA FLJ12443 FIS, CLONE NT2RM1000186" (SEQ ID No:63) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ 12443 FIS, CLONE NT2RM1000186" encoded by a nucleic acid that hybridizes to the "CDNA FLJ12443 FIS, CLONE NT2RM1000186" nucleic acid or its complement under low stringency conditions, and/or

(vii) "CDNA FLJ12681 FIS, CLONE NT2RM4002446" (SEQ ID No:64) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ12681 FIS, CLONE NT2RM4002446" encoded by a nucleic acid that hybridizes to the "CDNA FLJ12681 FIS, CLONE NT2RM4002446" nucleic acid or its complement under low stringency conditions, and/or 210

(viii) "CDNA FLJ13149 FIS, CLONE NT2RP3003344" (SEQ ID No:65) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ13149 FIS, CLONE NT2RP3003344" encoded by a nucleic acid that hybridizes to the "CDNA FLJ13149 FIS, CLONE NT2RP3003344" nucleic acid or its complement under low stringency conditions, and/or

(ix) "CDNA FLJ13716 FIS, CLONE PLACE2000411 " (SEQ ID No:66) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ13716 FIS, CLONE PLACE2000411 " encoded by a nucleic acid that hybridizes to the "CDNA FLJ13716 FIS, CLONE PLACE2000411 " nucleic acid or its complement under low stringency conditions, and/or

(x) "CDNA: FLJ22087 FIS, CLONE HEP15918" (SEQ ID No:67) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA: FLJ22087 FIS, CLONE HEP15918" encoded by a nucleic acid that hybridizes to the "CDNA: FLJ22087 FIS, CLONE HEP15918" nucleic acid or its complement under low stringency conditions, and/or

(xi) "CDP-DIACYLGLYCEROL-INOSITOL 3-PHOSPHATIDYLTRANSFERASE" (SEQ ID No:68) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDP-DIACYLGLYCEROL-INOSITOL 3- PHOSPHATIDYLTRANSFERASE" encoded by a nucleic acid that hybridizes to the "CDP-DIACYLGLYCEROL-INOSITOL 3-PHOSPHATIDYLTRANSFERASE" nucleic acid or its complement under low stringency conditions, and/or

(xii) "CHROMATIN-SPECIFIC TRANSCRIPTION ELONGATION FACTOR FACT 140 KDA SUBUNIT" (SEQ ID No:69) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CHROMATIN- SPECIFIC TRANSCRIPTION ELONGATION FACTOR FACT 140 KDA SUBUNIT" encoded by a nucleic acid that hybridizes to the "CHROMATIN-SPECIFIC TRANSCRIPTION ELONGATION FACTOR FACT 140 KDA SUBUNIT" nucleic acid or its complement under low stringency conditions, and/or

(xiii) "COLLAPSIN RESPONSE MEDIATOR PROTEIN-5" (SEQ ID No:70) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "COLLAPSIN RESPONSE MEDIATOR PROTEIN-5" encoded by a nucleic acid that hybridizes to the "COLLAPSIN RESPONSE MEDIATOR PROTEIN-5" nucleic acid or its complement under low stringency conditions, and/or 211

(xiv) "DIHYDROPYRIMIDINASE RELATED PROTEIN-5" (SEQ ID No:71) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "DIHYDROPYRIMIDINASE RELATED PROTEIN-5" encoded by a nucleic acid that hybridizes to the "DIHYDROPYRIMIDINASE RELATED PROTEIN-5" nucleic acid or its complement under low stringency conditions, and/or (xv) "DOPAMINE-RESPONSIVE PROTEIN" (SEQ ID No:72) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "DOPAMINE-RESPONSIVE PROTEIN" encoded by a nucleic acid that hybridizes to the "DOPAMINE-RESPONSIVE PROTEIN" nucleic acid or its complement under low stringency conditions, and/or

(xvi) "Diacylglycerol kinase epsilon" (SEQ ID No:73) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Diacylglycerol kinase epsilon" encoded by a nucleic acid that hybridizes to the "Diacylglycerol kinase epsilon" nucleic acid or its complement under low stringency conditions, and/or

(xvii) "EXCITATORY AMINO ACID TRANSPORTER 1 " (SEQ ID No:74) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "EXCITATORY AMINO ACID TRANSPORTER 1 " encoded by a nucleic acid that hybridizes to the "EXCITATORY AMINO ACID TRANSPORTER 1 " nucleic acid or its complement under low stringency conditions, and/or

(xviii) "FILAMIN A" (SEQ ID No:75) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "FILAMIN A" encoded by a nucleic acid that hybridizes to the "FILAMIN A" nucleic acid or its complement under low stringency conditions, and/or

(xix) "GPI8 PROTEIN (FRAGMENT)" (SEQ ID No:76) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "GPI8 PROTEIN (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "GPI8 PROTEIN (FRAGMENT)" nucleic acid or its complement under low stringency conditions, and/or

(xx) "Grb2" (SEQ ID No:77) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Grb2" encoded by a nucleic acid that hybridizes to the "Grb2" nucleic acid or its complement under low stringency conditions, and/or 212

(xxi) "HPT PROTEIN PRECURSOR" (SEQ ID No:78) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HPT PROTEIN PRECURSOR" encoded by a nucleic acid that hybridizes to the "HPT PROTEIN PRECURSOR" nucleic acid or its complement under low stringency conditions, and/or

(xxii) "HSGCN1 (FRAGMENT)" (SEQ ID No:79) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HSGCN1 (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "HSGCN1 (FRAGMENT)" nucleic acid or its complement under low stringency conditions, and/or (xxiii) "HYPOTHETICAL 35.7 KDA PROTEIN" (SEQ ID No:80) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYPOTHETICAL 35.7 KDA PROTEIN" encoded by a nucleic acid that hybridizes to the "HYPOTHETICAL 35.7 KDA PROTEIN" nucleic acid or its complement under low stringency conditions, and/or

(xxiv) "HYPOTHETICAL 68.1 KDA PROTEIN" (SEQ ID No:81) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYPOTHETICAL 68.1 KDA PROTEIN" encoded by a nucleic acid that hybridizes to the "HYPOTHETICAL 68.1 KDA PROTEIN" nucleic acid or its complement under low stringency conditions, and/or

(xxv) "HYPOTHETICAL PROTEIN XP_058906" (SEQ ID No:82) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYPOTHETICAL PROTEIN XP_058906" encoded by a nucleic acid that hybridizes to the "HYPOTHETICAL PROTEIN XP_058906" nucleic acid or its complement under low stringency conditions, and/or

(xxvi) "Heat shock protein 90, alpha" (SEQ ID No:83) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Heat shock protein 90, alpha" encoded by a nucleic acid that hybridizes to the "Heat shock protein 90, alpha" nucleic acid or its complement under low stringency conditions, and/or

(xxvii) "Her2" (SEQ ID No:84) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Her2" encoded by a nucleic acid that hybridizes to the "Her2" nucleic acid or its complement under low stringency conditions, and/or 213

(xxviii) "Her4" (SEQ ID No:85) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Her4" encoded by a nucleic acid that hybridizes to the "Her4" nucleic acid or its complement under low stringency conditions, and/or

(xxix) "INSULIN RECEPTOR SUBSTRATE 4" (SEQ ID No:86) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homoiog thereof, or a variant of "INSULIN RECEPTOR SUBSTRATE 4" encoded by a nucleic acid that hybridizes to the "INSULIN RECEPTOR SUBSTRATE 4" nucleic acid or its complement under low stringency conditions, and/or

(xxx) "KIAA0667 PROTEIN (FRAGMENT)" (SEQ ID No:87) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA0667 PROTEIN (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "KIAA0667 PROTEIN (FRAGMENT)" nucleic acid or its complement under low stringency conditions, and/or

(xxxii) "KIAA0887 PROTEIN (FRAGMENT)" (SEQ ID No:88) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA0887 PROTEIN (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "KIAA0887 PROTEIN (FRAGMENT)" nucleic acid or its complement under low stringency conditions, and/or

PRECURSOR" encoded by a nucleic acid that hybridizes to the "PALMITOYL-PROTEIN

THIOESTERASE 1 PRECURSOR" nucleic acid or its complement under low stringency conditions, and/or

(xxxiv) "PI3 kinase regulatory subunit p55 gamma" (SEQ ID No:90) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PI3 kinase regulatory subunit p55 gamma" encoded by a nucleic acid that hybridizes to the "PI3 kinase regulatory subunit p55 gamma" nucleic acid or its complement under low stringency conditions, and/or 214

(xxxv) "PI3 kinase regulatory subunit p85 alpha" (SEQ ID No:91) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PI3 kinase regulatory subunit p85 alpha" encoded by a nucleic acid that hybridizes to the "PI3 kinase regulatory subunit p85 alpha" nucleic acid or its complement under low stringency conditions, and/or

(xxxvi) "PI3 kinase regulatory subunit p85 beta" (SEQ ID No:92) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PI3 kinase regulatory subunit p85 beta" encoded by a nucleic acid that hybridizes to the "PI3 kinase regulatory subunit p85 beta" nucleic acid or its complement under low stringency conditions, and/or

(xxxvii) "PROCOLLAGEN-PROLINE, 2-OXOGLUTARATE 4-DIOXYGENASE (PROLINE 4- HYDROXYLASE), ALPHA POLYPEPTIDE I" (SEQ ID No:93) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PROCOLLAGEN-PROLINE, 2-OXOGLUTARATE 4-DIOXYGENASE (PROLINE 4- HYDROXYLASE), ALPHA POLYPEPTIDE I" encoded by a nucleic acid that hybridizes to the "PROCOLLAGEN-PROLINE, 2-OXOGLUTARATE 4- DIOXYGENASE (PROLINE 4- HYDROXYLASE), ALPHA POLYPEPTIDE I" nucleic acid or its complement under low stringency conditions, and/or

(xxxviii) "RIBONUCLEOSIDE-DIPHOSPHATE REDUCTASE M2 CHAIN" (SEQ ID No:94) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "RIBONUCLEOSIDE-DIPHOSPHATE REDUCTASE M2 CHAIN" encoded by a nucleic acid that hybridizes to the "RIBONUCLEOSIDE-DIPHOSPHATE REDUCTASE M2 CHAIN" nucleic acid or its complement under low stringency conditions, and/or

(xxxix) "SEL-1 HOMOLOG PRECURSOR" (SEQ ID No:95) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SEL-1 HOMOLOG PRECURSOR" encoded by a nucleic acid that hybridizes to the "SEL-1 HOMOLOG PRECURSOR" nucleic acid or its complement under low stringency conditions, and/or

(xl) "SHC" (SEQ ID No:96) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SHC" encoded by a nucleic acid that hybridizes to the "SHC" nucleic acid or its complement under low stringency conditions, and/or 215

(xii) "SIMILAR TO ADP.ATP CARRIER PROTEIN" (SEQ ID No:97) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SIMILAR TO ADP.ATP CARRIER PROTEIN" encoded by a nucleic acid that hybridizes to the "SIMILAR TO ADP.ATP CARRIER PROTEIN" nucleic acid or its complement under low stringency conditions, and/or

(xiii) "SIMILAR TO SIDEROFLEXIN 4" (SEQ ID No:98) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of

"SIMILAR TO SIDEROFLEXIN 4" encoded by a nucleic acid that hybridizes to the

"SIMILAR TO SIDEROFLEXIN 4" nucleic acid or its complement under low stringency conditions, and/or

"SPHINGOSINE KINASE 2" encoded by a nucleic acid that hybridizes to the

"SPHINGOSINE KINASE 2" nucleic acid or its complement under low stringency conditions, and/or

(xliv) "TRANSFERRIN RECEPTOR (P90, CD71)" (SEQ ID No: 100) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TRANSFERRIN RECEPTOR (P90, CD71)" encoded by a nucleic acid that hybridizes to the "TRANSFERRIN RECEPTOR (P90, CD71)" nucleic acid or its complement under low stringency conditions, and/or

(xiv) "TRANSFERRIN RECEPTOR PROTEIN 1 " (SEQ ID No:101) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TRANSFERRIN RECEPTOR PROTEIN 1 " encoded by a nucleic acid that hybridizes to the "TRANSFERRIN RECEPTOR PROTEIN 1" nucleic acid or its complement under low stringency conditions, and/or

(xlvi) "UV-DAMAGED DNA BINDING FACTOR" (SEQ ID No:102) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "UV-DAMAGED DNA BINDING FACTOR" encoded by a nucleic acid that hybridizes to the "UV-DAMAGED DNA BINDING FACTOR" nucleic acid or its complement under low stringency conditions, and/or

(xlvii) "VAMP-ASSOCIATED PROTEIN B" (SEQ ID No:103) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "VAMP-ASSOCIATED PROTEIN B" encoded by a nucleic acid that hybridizes 216

to the "VAMP-ASSOCIATED PROTEIN B" nucleic acid or its complement under low stringency conditions, and/or

(xlviii) "VAV-2" (SEQ ID No:104) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "VAV-2" encoded by a nucleic acid that hybridizes to the "VAV-2" nucleic acid or its complement under low stringency conditions, and/or

(xlix) "VAV-3" (SEQ ID No:105) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "VAV-3" encoded by a nucleic acid that hybridizes to the "VAV-3" nucleic acid or its complement under low stringency conditions, and/or

(I) "WD-REPEAT PROTEIN 6" (SEQ ID No:106) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "WD-REPEAT PROTEIN 6" encoded by a nucleic acid that hybridizes to the "WD- REPEAT PROTEIN 6" nucleic acid or its complement under low stringency conditions, and/or

(Ii) "WUGSC:H_RG122E10.2A PROTEIN" (SEQ ID No:107) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "WUGSC:H_RG122E10.2A PROTEIN" encoded by a nucleic acid that hybridizes to the "WUGSC:H_RG122E10.2A PROTEIN" nucleic acid or its complement under low stringency conditions, and/or

(Hi) "EGFR" (SEQ ID No:182) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "EGFR" encoded by a nucleic acid that hybridizes to the "EGFR" nucleic acid or its complement under low stringency conditions, and/or

(liii) "Erbin" (SEQ ID No:183) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Erbin" encoded by a nucleic acid that hybridizes to the "Erbin" nucleic acid or its complement under low stringency conditions, and/or

(liv) "GAP" (SEQ ID No:184) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "GAP" encoded by a nucleic acid that hybridizes to the "GAP" nucleic acid or its complement under low stringency conditions, and/or

(Iv) "Grb7" (SEQ ID No:185) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Grb7" encoded by a 217

nucleic acid that hybridizes to the "Grb7" nucleic acid or its complement under low stringency conditions, and/or

(Ivi) "Her3" (SEQ ID No:186) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Her3" encoded by a nucleic acid that hybridizes to the "Her3" nucleic acid or its complement under low stringency conditions, and/or

(Ivii) "PLC gamma" (SEQ ID No:187) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PLC gamma" encoded by a nucleic acid that hybridizes to the "PLC gamma" nucleic acid or its complement under low stringency conditions is present in the complex.

32. The method of any of No. 26 - 31 , wherein said method is a method of screening for a drug for treatment or prevention of a disease or disorder such as cancer such as breast cancer, ovarian cancer, lung cancer, stomach cancer, bladder cancer.

33. Use of a molecule that modulates the amount of, activity of, or the protein components of the complex of any one of No. 1 - 8 for the manufacture of a medicament for the treatment or prevention of a disease or disorder such as cancer such as breast cancer, ovarian cancer, lung cancer, stomach cancer, bladder cancer.

34. A method for the production of a pharmaceutical composition comprising carrying out the method of any of No. 1 - 8 to identify a molecule that modulates the function, activity, composition or formation of said complex, and further comprising mixing the identified molecule with a pharmaceutically acceptable carrier.

35. A method for diagnosing or screening for the presence of a disease or disorder or a predisposition for developing a disease or disorder in a subject, which disease or disorder is characterized by an aberrant amount of, activity of, or component composition of, or intracellular localization of the complex of any one of the No. 1 - 8, comprising determining the amount of, activity of, protein components of, and/or intracellular localization of, said complex and/or the transcription level of a gene dependent on the complex and/or the abundance and/or activity of a protein or protein complex dependent on the function of the complex and/or product of a gene dependent on the complex in a 218

comparative sample derived from a subject, wherein a difference in said amount, activity, or protein components of, said complex in an analogous sample from a subject not having the disease or disorder or predisposition indicates the presence in the subject of the disease or disorder or predisposition in the subject.

36. The method of No. 35, wherein the amount of said complex is determined.

37. The method of No. 35, wherein the activity of said complex is determined.

40. The method of No. 39, wherein said determining step comprises determining whether (i) "ALZHEIMER'S DISEASE AMYLOID A4 PROTEIN PRECURSOR" (SEQ ID No:58) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ALZHEIMER'S DISEASE AMYLOID A4 PROTEIN PRECURSOR" encoded by a nucleic acid that hybridizes to the "ALZHEIMER'S DISEASE AMYLOID A4 PROTEIN PRECURSOR" nucleic acid or its complement under low stringency conditions, and/or

(ii) "ANCIENT UBIQUITOUS PROTEIN 1 PRECURSOR" (SEQ ID No:59) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ANCIENT UBIQUITOUS PROTEIN 1 PRECURSOR" encoded by a nucleic acid that hybridizes to the "ANCIENT UBIQUITOUS PROTEIN 1 PRECURSOR" nucleic acid or its complement under low stringency conditions, and/or (iii) "ATP-DEPENDENT METALLOPROTEASE FTSH1 HOMOLOG" (SEQ ID No:60) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ATP-DEPENDENT METALLOPROTEASE FTSH1 219

HOMOLOG" encoded by a nucleic acid that hybridizes to the "ATP-DEPENDENT

METALLOPROTEASE FTSH1 HOMOLOG" nucleic acid or its complement under low stringency conditions, and/or

HOMOLOG" encoded by a nucleic acid that hybridizes to the "CDC37 HOMOLOG" nucleic acid or its complement under low stringency conditions, and/or

(vi) "CDNA FLJ12443 FIS, CLONE NT2RM1000186" (SEQ ID No:63) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ12443 FIS, CLONE NT2RM1000186" encoded by a nucleic acid that hybridizes to the "CDNA FLJ12443 FIS, CLONE NT2RM1000186" nucleic acid or its complement under low stringency conditions, and/or

(vii) "CDNA FLJ12681 FIS, CLONE NT2RM4002446" (SEQ ID No:64) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ12681 FIS, CLONE NT2RM4002446" encoded by a nucleic acid that hybridizes to the "CDNA FLJ12681 FIS, CLONE NT2RM4002446" nucleic acid or its complement under low stringency conditions, and/or

(ix) "CDNA FLJ13716 FIS, CLONE PLACE2000411" (SEQ ID No:66) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA FLJ13716 FIS, CLONE PLACE2000411" encoded by a nucleic acid that hybridizes to the "CDNA FLJ13716 FIS, CLONE PLACE2000411" nucleic acid or its complement under low stringency conditions, and/or

(x) "CDNA: FLJ22087 FIS, CLONE HEP15918" (SEQ ID No:67) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a 220

variant of "CDNA: FLJ22087 FIS, CLONE HEP15918" encoded by a nucleic acid that hybridizes to the "CDNA: FLJ22087 FIS, CLONE HEP15918" nucleic acid or its complement under low stringency conditions, and/or

(xiii) "COLLAPSIN RESPONSE MEDIATOR PROTEIN-5" (SEQ ID No:70) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "COLLAPSIN RESPONSE MEDIATOR PROTEIN-5" encoded by a nucleic acid that hybridizes to the "COLLAPSIN RESPONSE MEDIATOR PROTEIN-5" nucleic acid or its complement under low stringency conditions, and/or (xiv) "DIHYDROPYRIMIDINASE RELATED PROTEIN-5" (SEQ ID No:71) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "DIHYDROPYRIMIDINASE RELATED PROTEIN-5" encoded by a nucleic acid that hybridizes to the "DIHYDROPYRIMIDINASE RELATED PROTEIN-5" nucleic acid or its complement under low stringency conditions, and/or (xv) "DOPAMINE-RESPONSIVE PROTEIN" (SEQ ID No:72) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "DOPAMINE-RESPONSIVE PROTEIN" encoded by a nucleic acid that hybridizes to the "DOPAMINE-RESPONSIVE PROTEIN" nucleic acid or its complement under low stringency conditions, and/or

(xvi) "Diacylglycerol kinase epsilon" (SEQ ID No:73) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Diacylglycerol kinase epsilon" encoded by a nucleic acid that hybridizes to the 221

"Diacylglycerol kinase epsilon" nucleic acid or its complement under low stringency conditions, and/or

PROTEIN (FRAGMENT)" nucleic acid or its complement under low stringency conditions, and/or

(xx) "Grb2" (SEQ ID No:77) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Grb2" encoded by a nucleic acid that hybridizes to the "Grb2" nucleic acid or its complement under low stringency conditions, and/or

"HPT PROTEIN PRECURSOR" encoded by a nucleic acid that hybridizes to the "HPT

PROTEIN PRECURSOR" nucleic acid or its complement under low stringency conditions, and/or

"HSGCN1 (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "HSGCN1

(FRAGMENT)" nucleic acid or its complement under low stringency conditions, and/or

(xxiii) "HYPOTHETICAL 35.7 KDA PROTEIN" (SEQ ID No:80) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYPOTHETICAL 35.7 KDA PROTEIN" encoded by a nucleic acid that hybridizes to the "HYPOTHETICAL 35.7 KDA PROTEIN" nucleic acid or its complement under low stringency conditions, and/or 222

"Heat shock protein 90, alpha" encoded by a nucleic acid that hybridizes to the "Heat shock protein 90, alpha" nucleic acid or its complement under low stringency conditions, and/or

(xxvii) "Her2" (SEQ ID No:84) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Her2" encoded by a nucleic acid that hybridizes to the "Her2" nucleic acid or its complement under low stringency conditions, and/or

(xxix) "INSULIN RECEPTOR SUBSTRATE 4" (SEQ ID No:86) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "INSULIN RECEPTOR SUBSTRATE 4" encoded by a nucleic acid that hybridizes to the "INSULIN RECEPTOR SUBSTRATE 4" nucleic acid or its complement under low stringency conditions, and/or

(xxx) "K1AA0667 PROTEIN (FRAGMENT)" (SEQ ID No:87) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA0667 PROTEIN (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "KIAA0667 PROTEIN (FRAGMENT)" nucleic acid or its complement under low stringency conditions, and/or 223

PRECURSOR" encoded by a nucleic acid that hybridizes to the "PALMITOYL-PROTEIN

(xxxiv) "PI3 kinase regulatory subunit p55 gamma" (SEQ ID No:90) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PI3 kinase regulatory subunit p55 gamma" encoded by a nucleic acid that hybridizes to the "PI3 kinase regulatory subunit p55 gamma" nucleic acid or its complement under low stringency conditions, and/or

(xxxvii) "PROCOLLAGEN-PROLINE, 2-OXOGLUTARATE 4-DIOXYGENASE (PROLINE

4- HYDROXYLASE), ALPHA POLYPEPTIDE I" (SEQ ID No:93) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PROCOLLAGEN-PROLINE, 2-OXOGLUTARATE 4-DIOXYGENASE 224

DIOXYGENASE (PROLINE 4- HYDROXYLASE), ALPHA POLYPEPTIDE I" nucleic acid or its complement under low stringency conditions, and/or

(xxxviii) "RIBONUCLEOSIDE-DIPHOSPHATE REDUCTASE M2 CHAIN" (SEQ ID

REDUCTASE M2 CHAIN" encoded by a nucleic acid that hybridizes to the

"RIBONUCLEOSIDE-DIPHOSPHATE REDUCTASE M2 CHAIN" nucleic acid or its complement under low stringency conditions, and/or

(xl) "SHC" (SEQ ID No:96) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SHC" encoded by a nucleic acid that hybridizes to the "SHC" nucleic acid or its complement under low stringency conditions, and/or

(xii) "SIMILAR TO ADP.ATP CARRIER PROTEIN" (SEQ ID No:97) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SIMILAR TO ADP,ATP CARRIER PROTEIN" encoded by a nucleic acid that hybridizes to the "SIMILAR TO ADP.ATP CARRIER PROTEIN" nucleic acid or its complement under low stringency conditions, and/or

"SIMILAR TO SIDEROFLEXIN 4" encoded by a nucleic acid that hybridizes to the

"SPHINGOSINE KINASE 2" encoded by a nucleic acid that hybridizes to the

"SPHINGOSINE KINASE 2" nucleic acid or its complement under low stringency conditions, and/or 225

(xliv) "TRANSFERRIN RECEPTOR (P90, CD71)" (SEQ ID No:100) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TRANSFERRIN RECEPTOR (P90, CD71)" encoded by a nucleic acid that hybridizes to the "TRANSFERRIN RECEPTOR (P90, CD71)" nucleic acid or its complement under low stringency conditions, and/or

(xiv) "TRANSFERRIN RECEPTOR PROTEIN 1 " (SEQ ID No:101) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TRANSFERRIN RECEPTOR PROTEIN 1 " encoded by a nucleic acid that hybridizes to the "TRANSFERRIN RECEPTOR PROTEIN 1 " nucleic acid or its complement under low stringency conditions, and/or

(xlvii) "VAMP-ASSOCIATED PROTEIN B" (SEQ ID No:103) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "VAMP-ASSOCIATED PROTEIN B" encoded by a nucleic acid that hybridizes to the "VAMP-ASSOCIATED PROTEIN B" nucleic acid or its complement under low stringency conditions, and/or

(I) "WD-REPEAT PROTEIN 6" (SEQ ID No:106) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "WD-REPEAT PROTEIN 6" encoded by a nucleic acid that hybridizes to the "WD- REPEAT PROTEIN 6" nucleic acid or its complement under low stringency conditions, and/or 226

(Iii) "EGFR" (SEQ ID No:182) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "EGFR" encoded by a nucleic acid that hybridizes to the "EGFR" nucleic acid or its complement under low stringency conditions, and/or

(liii) "Erbin" (SEQ ID No: 183) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Erbin" encoded by a

( nucleic acid that hybridizes to the "Erbin" nucleic acid or its complement under low stringency conditions, and/or

(Iv) "Grb7" (SEQ ID No:185) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Grb7" encoded by a nucleic acid that hybridizes to the "Grb7" nucleic acid or its complement under low stringency conditions, and/or

41. The complex of any one of No. 1 - 8, or proteins of No. 13 or the antibody or fragment of No. 17, for use in a method of diagnosing a disease or disorder such as 227

cancer such as breast cancer, ovarian cancer, lung cancer, stomach cancer, bladder cancer.

42. A method for treating or preventing a disease or disorder characterized by an aberrant amount of, activity or component composition of or intracellular localization of, the complex of anyone of No. 1 - 8, comprising administering to a subject in need of such treatment or prevention a therapeutically effective amount of one or more molecules that modulate the amount of, kinase activity, diacylglycerol kinase activity or sphingosine kinase activity, or protein components of, said complex.

(ii) "ANCIENT UBIQUITOUS PROTEIN 1 PRECURSOR" (SEQ ID No:59) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ANCIENT UBIQUITOUS PROTEIN 1 PRECURSOR" encoded by a nucleic acid that hybridizes to the "ANCIENT UBIQUITOUS PROTEIN 1 PRECURSOR" nucleic acid or its complement under low stringency conditions, (iii) "ATP-DEPENDENT METALLOPROTEASE FTSH1 HOMOLOG" (SEQ ID No:60) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ATP-DEPENDENT METALLOPROTEASE FTSH1 HOMOLOG" encoded by a nucleic acid that hybridizes to the "ATP-DEPENDENT METALLOPROTEASE FTSH1 HOMOLOG" nucleic acid or its complement under low stringency conditions, 228

(x) "CDNA: FLJ22087 FIS, CLONE HEP15918" (SEQ ID No:67) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CDNA: FLJ22087 FIS, CLONE HEP15918" encoded by a nucleic acid that hybridizes to the "CDNA: FLJ22087 FIS, CLONE HEP15918" nucleic acid or its complement under low stringency conditions, 229

(xvi) "Diacylglycerol kinase epsilon" (SEQ ID No:73) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Diacylglycerol kinase epsilon" encoded by a nucleic acid that hybridizes to the "Diacylglycerol kinase epsilon" nucleic acid or its complement under low stringency conditions, 230

(xvii) "EXCITATORY AMINO ACID TRANSPORTER 1" (SEQ ID No:74) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "EXCITATORY AMINO ACID TRANSPORTER 1 " encoded by a nucleic acid that hybridizes to the "EXCITATORY AMINO ACID TRANSPORTER 1" nucleic acid or its complement under low stringency conditions,

"HPT PROTEIN PRECURSOR" encoded by a nucleic acid that hybridizes to the "HPT

"HSGCN1 (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "HSGCN1

(FRAGMENT)" nucleic acid or its complement under low stringency conditions,

(xxiv) "HYPOTHETICAL 68.1 KDA PROTEIN" (SEQ ID No:81) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a 231

variant of "HYPOTHETICAL 68.1 KDA PROTEIN" encoded by a nucleic acid that hybridizes to the "HYPOTHETICAL 68.1 KDA PROTEIN" nucleic acid or its complement under low stringency conditions,

PROTEIN" encoded by a nucleic acid that hybridizes to the "KIAA0792 PROTEIN" nucleic acid or its complement under low stringency conditions, 232

(xxxiii) "PALMITOYL-PROTEIN THIOESTERASE 1 PRECURSOR" (SEQ ID No:89) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PALMITOYL-PROTEIN THIOESTERASE 1 PRECURSOR" encoded by a nucleic acid that hybridizes to the "PALMITOYL-PROTEIN THIOESTERASE 1 PRECURSOR" nucleic acid or its complement under low stringency conditions,

(xxxiv) "Pl3 kinase regulatory subunit p55 gamma" (SEQ ID No:90) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PI3 kinase regulatory subunit p55 gamma" encoded by a nucleic acid that hybridizes to the "PI3 kinase regulatory subunit p55 gamma" nucleic acid or its complement under low stringency conditions,

(xxxvii) "PROCOLLAGEN-PROLINE, 2-OXOGLUTARATE 4-DIOXYGENASE (PROLINE 4- HYDROXYLASE), ALPHA POLYPEPTIDE I" (SEQ ID No:93) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PROCOLLAGEN-PROLINE, 2-OXOGLUTARATE 4-DIOXYGENASE (PROLINE 4- HYDROXYLASE), ALPHA POLYPEPTIDE I" encoded by a nucleic acid that hybridizes to the "PROCOLLAGEN-PROLINE, 2-OXOGLUTARATE 4- DIOXYGENASE (PROLINE 4- HYDROXYLASE), ALPHA POLYPEPTIDE I" nucleic acid or its complement under low stringency conditions, 233

(xxxviii) "RIBONUCLEOSIDE-DIPHOSPHATE REDUCTASE M2 CHAIN" (SEQ ID

REDUCTASE M2 CHAIN" encoded by a nucleic acid that hybridizes to the

"SIMILAR TO SIDEROFLEXIN 4" encoded by a nucleic acid that hybridizes to the

"SPHINGOSINE KINASE 2" encoded by a nucleic acid that hybridizes to the

(xliv) "TRANSFERRIN RECEPTOR (P90, CD71)" (SEQ ID No:100) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TRANSFERRIN RECEPTOR (P90, CD71)" encoded by a nucleic acid 234

that hybridizes to the "TRANSFERRIN RECEPTOR (P90, CD71)" nucleic acid or its complement under low stringency conditions,

(xiv) "TRANSFERRIN RECEPTOR PROTEIN 1 " (SEQ ID No: 101) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TRANSFERRIN RECEPTOR PROTEIN 1 " encoded by a nucleic acid that hybridizes to the "TRANSFERRIN RECEPTOR PROTEIN 1 " nucleic acid or its complement under low stringency conditions,

(I) "WD-REPEAT PROTEIN 6" (SEQ ID No:106) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "WD-REPEAT PROTEIN 6" encoded by a nucleic acid that hybridizes to the "WD- REPEAT PROTEIN 6" nucleic acid or its complement under low stringency conditions, and/or(li) "WUGSC:H_RG122E10.2A PROTEIN" (SEQ ID No:107) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "WUGSC:H_RG122E10.2A PROTEIN" encoded by a nucleic acid that hybridizes to the "WUGSC:H_RG122E10.2A PROTEIN" nucleic acid or its complement under low stringency conditions, 235

(Iii) "EGFR" (SEQ ID No:182) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "EGFR" encoded by a nucleic acid that hybridizes to the "EGFR" nucleic acid or its complement under low stringency conditions,

(liii) "Erbin" (SEQ ID No:183) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Erbin" encoded by a nucleic acid that hybridizes to the "Erbin" nucleic acid or its complement under low stringency conditions,

(liv) "GAP" (SEQ ID No:184) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "GAP" encoded by a nucleic acid that hybridizes to the "GAP" nucleic acid or its complement under low stringency conditions,

(Iv) "Grb7" (SEQ ID No:185) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Grb7" encoded by a nucleic acid that hybridizes to the "Grb7" nucleic acid or its complement under low stringency conditions,

(Ivi) "Her3" (SEQ ID No:186) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Her3" encoded by a nucleic acid that hybridizes to the "Her3" nucleic acid or its complement under low stringency conditions,

(Ivii) "PLC gamma" (SEQ ID No: 187) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PLC gamma" encoded by a nucleic acid that hybridizes to the "PLC gamma" nucleic acid or its complement under low stringency conditions as a target for an active agent of a pharmaceutical, preferably a drug target in the treatment or prevention of a disease or disorder such as cancer such as breast cancer, ovarian cancer, lung cancer, stomach cancer, bladder cancer.

Thus, the invention further relates to the following embodiments of the Ringol -protein complex

1. A protein complex selected from complex (I) and comprising (a) at least one first protein selected from the group consisting of: 236

(i) "Ringol " (SEQ ID No:125) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Ringol " encoded by a nucleic acid that hybridizes to the "Ringol " nucleic acid or its complement under low stringency conditions,

(ii) "cdc2" (SEQ ID No:128) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "cdc2" encoded by a nucleic acid that hybridizes to the "cdc2" nucleic acid or its complement under low stringency conditions, and

(iii) "cdk2" (SEQ ID No:129) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "cdk2" encoded by a nucleic acid that hybridizes to the "cdk2" nucleic acid or its complement under low stringency conditions, and

(i) "BROMODOMAIN-CONTAINING PROTEIN 2" (SEQ ID No:108) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "BROMODOMAIN-CONTAINING PROTEIN 2" encoded by a nucleic acid that hybridizes to the "BROMODOMAIN-CONTAINING PROTEIN 2" nucleic acid or its complement under low stringency conditions,

(ii) "BROMODOMAIN-CONTAINING PROTEIN 4" (SEQ ID No:109) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "BROMODOMAIN-CONTAINING PROTEIN 4" encoded by a nucleic acid that hybridizes to the "BROMODOMAIN-CONTAINING PROTEIN 4" nucleic acid or its complement under low stringency conditions,

(iii) "CELL DIVISION PROTEIN KINASE 5" (SEQ ID No:110) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CELL DIVISION PROTEIN KINASE 5" encoded by a nucleic acid that hybridizes to the "CELL DIVISION PROTEIN KINASE 5" nucleic acid or its complement under low stringency conditions,

(iv) "DNA TOPOISOMERASE I" (SEQ ID No:111) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of

"DNA TOPOISOMERASE l" encoded by a nucleic acid that hybridizes to the "DNA

TOPOISOMERASE I" nucleic acid or its complement under low stringency conditions, 237

(v) "HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN M, ISOFORM A" (SEQ ID No: 112) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN M, ISOFORM A" encoded by a nucleic acid that hybridizes to the "HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN M, ISOFORM A" nucleic acid or its complement under low stringency conditions,

(vi) "HYPOTHETICAL 24.3 KDA PROTEIN" (SEQ ID No:113) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYPOTHETICAL 24.3 KDA PROTEIN" encoded by a nucleic acid that hybridizes to the "HYPOTHETICAL 24.3 KDA PROTEIN" nucleic acid or its complement under low stringency conditions,

(vii) "HYPOTHETICAL PROTEIN XP_089560" (SEQ ID No:114) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYPOTHETICAL PROTEIN XP_089560" encoded by a nucleic acid that hybridizes to the "HYPOTHETICAL PROTEIN XP_089560" nucleic acid or its complement under low stringency conditions,

(viii) "IGF-ll MRNA-BINDING PROTEIN 3" (SEQ ID No:115) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "IGF-ll MRNA-BINDING PROTEIN 3" encoded by a nucleic acid that hybridizes to the "IGF-ll MRNA-BINDING PROTEIN 3" nucleic acid or its complement under low stringency conditions,

(ix) "MYB-BINDING PROTEIN 1A" (SEQ ID No:116) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "MYB-BINDING PROTEIN 1A" encoded by a nucleic acid that hybridizes to the "MYB- BINDING PROTEIN 1 A" nucleic acid or its complement under low stringency conditions, (x) "NUCLEAR MATRIX PROTEIN NMP200" (SEQ ID No:117) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "NUCLEAR MATRIX PROTEIN NMP200" encoded by a nucleic acid that hybridizes to the "NUCLEAR MATRIX PROTEIN NMP200" nucleic acid or its complement under low stringency conditions,

(xi) "NUCLEOLAR PROTEIN NOP56" (SEQ ID No:118) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "NUCLEOLAR PROTEIN NOP56" encoded by a nucleic acid that hybridizes to the 238

"NUCLEOLAR PROTEIN NOP56" nucleic acid or its complement under low stringency conditions,

(xii) "NUCLEOLAR RNA HELICASE II" (SEQ ID No:119) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "NUCLEOLAR RNA HELICASE II" encoded by a nucleic acid that hybridizes to the "NUCLEOLAR RNA HELICASE II" nucleic acid or its complement under low stringency conditions,

(xiii) "NUCLEOPHOSMIN" (SEQ ID No:120) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "NUCLEOPHOSMIN" encoded by a nucleic acid that hybridizes to the "NUCLEOPHOSMIN" nucleic acid or its complement under low stringency conditions, (xiv) "NUCLEOPLASMIN 3" (SEQ ID No:121) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "NUCLEOPLASMIN 3" encoded by a nucleic acid that hybridizes to the "NUCLEOPLASMIN 3" nucleic acid or its complement under low stringency conditions, (xv) "POMBE CDC5-RELATED PROTEIN" (SEQ ID No:122) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "POMBE CDC5-RELATED PROTEIN" encoded by a nucleic acid that hybridizes to the "POMBE CDC5-RELATED PROTEIN" nucleic acid or its complement under low stringency conditions,

(xvi) "PROLIFERATING-CELL NUCLEOLAR ANTIGEN P120" (SEQ ID No:123) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PROLIFERATING-CELL NUCLEOLAR ANTIGEN P120" encoded by a nucleic acid that hybridizes to the "PROLIFERATING-CELL NUCLEOLAR ANTIGEN P120" nucleic acid or its complement under low stringency conditions,

(xvii) "RRP5 PROTEIN HOMOLOG (FRAGMENT)" (SEQ ID No:124) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "RRP5 PROTEIN HOMOLOG (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "RRP5 PROTEIN HOMOLOG (FRAGMENT)" nucleic acid or its complement under low stringency conditions,

(xviii) "SIMILAR TO NUMB-ASSOCIATED KINASE" (SEQ ID No:126) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SIMILAR TO NUMB-ASSOCIATED KINASE" encoded by a nucleic acid 239

that hybridizes to the "SIMILAR TO NUMB-ASSOCIATED KINASE" nucleic acid or its complement under low stringency conditions, and

(xix) "SIMILAR TO RIKEN CDNA 1110064N10 GENE" (SEQ ID No:127) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SIMILAR TO RIKEN CDNA 1110064N10 GENE" encoded by a nucleic acid that hybridizes to the "SIMILAR TO RIKEN CDNA 1110064N10 GENE" nucleic acid or its complement under low stringency conditions, and a complex (II) comprising at least two of said second proteins, wherein said low stringency conditions comprise hybridization in a buffer comprising 35% formamide, 5X SSC, 50 mM Tris-HCI (pH 7.5), 5 mM EDTA, 0.02% PVP, 0.02% Ficoll, 0.2% BSA, 100 ug/ml denatured salmon sperm DNA, and 10% (wt/vol) dextran sulfate for 18-20 hours at 40 Celsius, washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4), 5 mM EDTA, and 0.1 % SDS for 1.5 hours at 55 Celsius, and washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4), 5 mM EDTA, and 0.1% SDS for 1.5 hours at 60 Celsius.

2. The protein complex according to No. 1 wherein the first protein is the protein Ringol (SEQ ID NO. 125), or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of 'Ringol' encoded by a nucleic acid that hybridizes to the 'Ringol ' under low stringency conditions.

(iii) "CELL DIVISION PROTEIN KINASE 5" (SEQ ID No:110) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a 240

variant of "CELL DIVISION PROTEIN KINASE 5" encoded by a nucleic acid that hybridizes to the "CELL DIVISION PROTEIN KINASE 5" nucleic acid or its complement under low stringency conditions,

(iv) "DNA TOPOISOMERASE I" (SEQ ID No:111) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "DNA TOPOISOMERASE I" encoded by a nucleic acid that hybridizes to the "DNA TOPOISOMERASE I" nucleic acid or its complement under low stringency conditions, (v) "HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN M, ISOFORM A" (SEQ ID No:112) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN M, ISOFORM A" encoded by a nucleic acid that hybridizes to the "HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN M, ISOFORM A" nucleic acid or its complement under low stringency conditions,

(ix) "MYB-BINDING PROTEIN 1A" (SEQ ID No:116) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "MYB-BINDING PROTEIN 1A" encoded by a nucleic acid that hybridizes to the "MYB- BINDING PROTEIN 1 A" nucleic acid or its complement under low stringency conditions, (x) "NUCLEAR MATRIX PROTEIN NMP200" (SEQ ID No:117) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a 241

variant of "NUCLEAR MATRIX PROTEIN NMP200" encoded by a nucleic acid that hybridizes to the "NUCLEAR MATRIX PROTEIN NMP200" nucleic acid or its complement under low stringency conditions,

(xi) "NUCLEOLAR PROTEIN NOP56" (SEQ ID No:118) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "NUCLEOLAR PROTEIN NOP56" encoded by a nucleic acid that hybridizes to the "NUCLEOLAR PROTEIN NOP56" nucleic acid or its complement under low stringency conditions,

(xvii) "RRP5 PROTEIN HOMOLOG (FRAGMENT)" (SEQ ID No:124) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, 242

or a variant of "RRP5 PROTEIN HOMOLOG (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "RRP5 PROTEIN HOMOLOG (FRAGMENT)" nucleic acid or its complement under low stringency conditions,

(xviii) "Ringol" (SEQ ID No:125) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Ringol " encoded by a nucleic acid that hybridizes to the "Ringol " nucleic acid or its complement under low stringency conditions,

(xix) "SIMILAR TO NUMB-ASSOCIATED KINASE" (SEQ ID No:126) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SIMILAR TO NUMB-ASSOCIATED KINASE" encoded by a nucleic acid that hybridizes to the "SIMILAR TO NUMB-ASSOCIATED KINASE" nucleic acid or its complement under low stringency conditions,

(xx) "SIMILAR TO RIKEN CDNA 1110064N10 GENE" (SEQ ID No:127) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SIMILAR TO RIKEN CDNA 1110064N10 GENE" encoded by a nucleic acid that hybridizes to the "SIMILAR TO RIKEN CDNA 1110064N10 GENE" nucleic acid or its complement under low stringency conditions,

(xxi) "cdc2" (SEQ ID No: 128) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "cdc2" encoded by a nucleic acid that hybridizes to the "cdc2" nucleic acid or its complement under low stringency conditions, and/or

(xxii) "cdk2" (SEQ ID No:129) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "cdk2" encoded by a nucleic acid that hybridizes to the "cdk2" nucleic acid or its complement under low stringency conditions, and a protein complex selected from complex (II) and comprising the following proteins:

(ii) "BROMODOMAIN-CONTAINING PROTEIN 4" (SEQ ID No:109) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "BROMODOMAIN-CONTAINING PROTEIN 4" encoded by a nucleic acid 243

that hybridizes to the "BROMODOMAIN-CONTAINING PROTEIN 4" nucleic acid or its complement under low stringency conditions,

(iii) "CELL DIVISION PROTEIN KINASE 5" (SEQ ID No: 110) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CELL DIVISION PROTEIN KINASE 5" encoded by a nucleic acid that hybridizes to the "CELL DIVISION PROTEIN KINASE 5" nucleic acid or its complement under low stringency conditions,

"DNA TOPOISOMERASE I" encoded by a nucleic acid that hybridizes to the "DNA

TOPOISOMERASE I" nucleic acid or its complement under low stringency conditions,

(v) "HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN M, ISOFORM A" (SEQ ID

No:112) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HETEROGENEOUS NUCLEAR

RIBONUCLEOPROTEIN M, ISOFORM A" encoded by a nucleic acid that hybridizes to the "HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN M, ISOFORM A" nucleic acid or its complement under low stringency conditions,

(ix) "MYB-BINDING PROTEIN 1A" (SEQ ID No:116) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of 244

"MYB-BINDING PROTEIN 1A" encoded by a nucleic acid that hybridizes to the "MYB- BINDING PROTEIN 1 A" nucleic acid or its complement under low stringency conditions, (x) "NUCLEAR MATRIX PROTEIN NMP200" (SEQ ID No:117) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "NUCLEAR MATRIX PROTEIN NMP200" encoded by a nucleic acid that hybridizes to the "NUCLEAR MATRIX PROTEIN NMP200" nucleic acid or its complement under low stringency conditions,

(xiii) "NUCLEOPHOSMIN" (SEQ ID No: 120) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "NUCLEOPHOSMIN" encoded by a nucleic acid that hybridizes to the "NUCLEOPHOSMIN" nucleic acid or its complement under low stringency conditions, (xiv) "NUCLEOPLASMIN 3" (SEQ ID No:121) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "NUCLEOPLASMIN 3" encoded by a nucleic acid that hybridizes to the "NUCLEOPLASMIN 3" nucleic acid or its complement under low stringency conditions, (xv) "POMBE CDC5-RELATED PROTEIN" (SEQ ID No: 122) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "POMBE CDC5-RELATED PROTEIN" encoded by a nucleic acid that hybridizes to the "POMBE CDC5-RELATED PROTEIN" nucleic acid or its complement under low stringency conditions,

(xvi) "PROLIFERATING-CELL NUCLEOLAR ANTIGEN P120" (SEQ ID No:123) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PROLIFERATING-CELL NUCLEOLAR ANTIGEN P120" encoded by a nucleic acid that hybridizes to the "PROLIFERATING-CELL 245

NUCLEOLAR ANTIGEN P120" nucleic acid or its complement under low stringency conditions,

(xviii) "Ringol " (SEQ ID No:125) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Ringol " encoded by a nucleic acid that hybridizes to the "Ringol " nucleic acid or its complement under low stringency conditions,

(xxi) "cdc2" (SEQ ID No:128) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "cdc2" encoded by a nucleic acid that hybridizes to the "cdc2" nucleic acid or its complement under low stringency conditions, and/or

(xxii) "cdk2" (SEQ ID No:129) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "cdk2" encoded by a nucleic acid that hybridizes to the "cdk2" nucleic acid or its complement under low stringency conditions, and a protein complex selected from complex (III) and comprising the following proteins:

(i) "BROMODOMAIN-CONTAINING PROTEIN 2" (SEQ ID No:108) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "BROMODOMAIN-CONTAINING PROTEIN 2" encoded by a nucleic acid 246 that hybridizes to the "BROMODOMAIN-CONTAINING PROTEIN 2" nucleic acid or its complement under low stringency conditions,

(iv) "NUCLEOPLASMIN 3" (SEQ ID No:121) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "NUCLEOPLASMIN 3" encoded by a nucleic acid that hybridizes to the "NUCLEOPLASMIN 3" nucleic acid or its complement under low stringency conditions,

(v) "Ringol " (SEQ ID No:125) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Ringol " encoded by a nucleic acid that hybridizes to the "Ringol " nucleic acid or its complement under low stringency conditions,

(vi) "cdc2" (SEQ ID No: 128) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "cdc2" encoded by a nucleic acid that hybridizes to the "cdc2" nucleic acid or its complement under low stringency conditions, and/or

(vii) "cdk2" (SEQ ID No:129) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "cdk2" encoded by a nucleic acid that hybridizes to the "cdk2" nucleic acid or its complement under low stringency conditions,

4. The protein complex according to No. 1 comprising all but 1 - 18 of the following proteins:

(i) "BROMODOMAIN-CONTAINING PROTEIN 2" (SEQ ID No:108) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "BROMODOMAIN-CONTAINING PROTEIN 2" encoded by a nucleic acid 247

that hybridizes to the "BROMODOMAIN-CONTAINING PROTEIN 2" nucleic acid or its complement under low stringency conditions,

"DNA TOPOISOMERASE I" encoded by a nucleic acid that hybridizes to the "DNA

(v) "HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN M, ISOFORM A" (SEQ ID

(vi) "HYPOTHETICAL 24.3 KDA PROTEIN" (SEQ ID No: 113) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYPOTHETICAL 24.3 KDA PROTEIN" encoded by a nucleic acid that hybridizes to the "HYPOTHETICAL 24.3 KDA PROTEIN" nucleic acid or its complement under low stringency conditions,

(viii) "IGF-ll MRNA-BINDING PROTEIN 3" (SEQ ID No:115) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a 248

variant of "IGF-ll MRNA-BINDING PROTEIN 3" encoded by a nucleic acid that hybridizes to the "IGF-ll MRNA-BINDING PROTEIN 3" nucleic acid or its complement under low stringency conditions,

(xiii) "NUCLEOPHOSMIN" (SEQ ID No:120) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "NUCLEOPHOSMIN" encoded by a nucleic acid that hybridizes to the "NUCLEOPHOSMIN" nucleic acid or its complement under low stringency conditions, (xiv) "NUCLEOPLASMIN 3" (SEQ ID No:121) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "NUCLEOPLASMIN 3" encoded by a nucleic acid that hybridizes to the "NUCLEOPLASMIN 3" nucleic acid or its complement under low stringency conditions, (xv) "POMBE CDC5-RELATED PROTEIN" (SEQ ID No:122) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "POMBE CDC5-RELATED PROTEIN" encoded by a nucleic acid that 249

hybridizes to the "POMBE CDC5-RELATED PROTEIN" nucleic acid or its complement under low stringency conditions,

(xvi) "PROLIFERATING-CELL NUCLEOLAR ANTIGEN P120" (SEQ ID No:123) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PROLIFERATING-CELL NUCLEOLAR ANTIGEN

P120" encoded by a nucleic acid that hybridizes to the "PROLIFERATING-CELL

(xxi) "cdc2" (SEQ ID No:128) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "cdc2" encoded by a nucleic acid that hybridizes to the "cdc2" nucleic acid or its complement under low stringency conditions,

(xxii) "cdk2" (SEQ ID No:129) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "cdk2" encoded by a 250

8. The complex of any of No. 1 - 7 that is involved in the kinase activation.

12. Component of the Ringo 1 complex obtainable by a process according to any of No. 9 - 11. 251

13. Protein of the Ringo 1 complex selected from

(i) "SIMILAR TO RIKEN CDNA 1110064N10 GENE" (SEQ ID No:127) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SIMILAR TO RIKEN CDNA 1110064N10 GENE" encoded by a nucleic acid that hybridizes to the "SIMILAR TO RIKEN CDNA 1110064N10 GENE" nucleic acid or its complement under low stringency conditions, wherein, said low stringency conditions comprise hybridization in a buffer comprising 35% formamide, 5X SSC, 50 mM Tris-HCI (pH 7.5), 5 mM EDTA, 0.02% PVP, 0.02% Ficoll, 0.2% BSA, 100 ug/ml denatured salmon sperm DNA, and 10% (wt/vol) dextran sulfate for 18-20 hours at 40 Celsius, washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4), 5 mM EDTA, and 0.1 % SDS for 1.5 hours at 55 Celsius, and washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4), 5 mM EDTA, and 0.1% SDS for 1.5 hours at 60 Celsius.

14. Nucleic acid encoding a protein according to No. 13.

16. Host cell, containing a vector comprising at least one of the nucleic acid of No. 14 and/or a construct of No. 15 or containing several vectors each comprising at least the nucleic acid sequence encoding at least one of the proteins, or functionally active fragments or functionally active derivatives thereof selected from the first group of proteins according to No. 1 (a) and the proteins, or functionally active fragments or 252

functionally active derivatives thereof selected from the second group of proteins according to No. 1 (b).

19. The kit according to No. 18 for processing a substrate of said complex. ,

20. The kit according to No. 18 for the diagnosis or prognosis of a disease or a disease risk, preferentially for a disease or disorder such as cancer such as breast cancer, lung cancer, colon cancer, prostate cancer, leukaemia;neurodegenerative diseases such as Alzheimer's disease and amyotrophic lateral sclerosis (ALS).

(i) "SIMILAR TO RIKEN CDNA 1110064N10 GENE" (SEQ ID No:127) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SIMILAR TO RIKEN CDNA 1110064N10 GENE" encoded by a nucleic acid that hybridizes to the "SIMILAR TO RIKEN CDNA 1110064N10 GENE" nucleic acid 253

or its complement under low stringency conditions, and a pharmaceutical acceptable carrier.

24. A pharmaceutical composition according to No. 23 for the treatment of diseases and disorders such as cancer such as breast cancer, lung cancer, colon cancer, prostate cancer, leukaemia;neurodegenerative diseases such as Alzheimer's disease and amyotrophic lateral sclerosis (ALS).

(i) "SIMILAR TO RIKEN CDNA 1110064N10 GENE" (SEQ ID No:127) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SIMILAR TO RIKEN CDNA 1110064N10 GENE" encoded by a nucleic acid that hybridizes to the "SIMILAR TO RIKEN CDNA 1110064N10 GENE" nucleic acid or its complement under low stringency conditions, comprising the steps of

(b) determinig whether said candidate molecule is bound to the complex or protein.

26. A method for screening for a molecule that modulates directly or indirectly the function, activity, composition or formation of the complex of any one of No. 1 - 8 comprising the steps of(a) exposing said complex, or a cell or organism containing Ringo 1 complex to one or more candidate molecules; and

(b) determining the amount of activity of protein components of, and/or intracellular localization of, said complex and/or the transcription level of a gene dependent on the complex and/or the abundance and/or activity of a protein or protein complex dependent on the function of the complex and/or product of a gene dependent on the complex in the presence of the one or more candidate molecules, wherein a change in said amount, activity, protein components or intracellular localization relative to said amount, activity, protein components and/or intracellular localization and/or a change in the transcription level of a gene dependent on the complex and/or the abundance and/or activity of a 254

protein or protein complex dependent on the function of the complex and/or product of a gene dependent on the complex in the absence of said candidate molecules indicates that the molecule modulates function, activity or composition of said complex.

27. The method of No. 26, wherein the amount of said complex is determined.

28. The method of No. 26, wherein the activity of said complex is determined.

31. The method of No. 30, wherein said determining step comprises determining whether (i) "BROMODOMAIN-CONTAINING PROTEIN 2" (SEQ ID No:108) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "BROMODOMAIN-CONTAINING PROTEIN 2" encoded by a nucleic acid that hybridizes to the "BROMODOMAIN-CONTAINING PROTEIN 2" nucleic acid or its complement under low stringency conditions, and/or

(ii) "BROMODOMAIN-CONTAINING PROTEIN 4" (SEQ ID No:109) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "BROMODOMAIN-CONTAINING PROTEIN 4" encoded by a nucleic acid that hybridizes to the "BROMODOMAIN-CONTAINING PROTEIN 4" nucleic acid or its complement under low stringency conditions, and/or

(iii) "CELL DIVISION PROTEIN KINASE 5" (SEQ ID No:110) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CELL DIVISION PROTEIN KINASE 5" encoded by a nucleic acid that hybridizes to the "CELL DIVISION PROTEIN KINASE 5" nucleic acid or its complement under low stringency conditions, and/or 255

(iv) "DNA TOPOISOMERASE I" (SEQ ID No:111) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "DNA TOPOISOMERASE I" encoded by a nucleic acid that hybridizes to the "DNA TOPOISOMERASE I" nucleic acid or its complement under low stringency conditions, and/or

(v) "HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN M, ISOFORM A" (SEQ ID No: 112) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN M, ISOFORM A" encoded by a nucleic acid that hybridizes to the "HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN M, ISOFORM A" nucleic acid or its complement under low stringency conditions, and/or

(vi) "HYPOTHETICAL 24.3 KDA PROTEIN" (SEQ ID No:113) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYPOTHETICAL 24.3 KDA PROTEIN" encoded by a nucleic acid that hybridizes to the "HYPOTHETICAL 24.3 KDA PROTEIN" nucleic acid or its complement under low stringency conditions, and/or

(vii) "HYPOTHETICAL PROTEIN XP_089560" (SEQ ID No:114) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYPOTHETICAL PROTEIN XP_089560" encoded by a nucleic acid that hybridizes to the "HYPOTHETICAL PROTEIN XP_089560" nucleic acid or its complement under low stringency conditions, and/or

(viii) "IGF-ll MRNA-BINDING PROTEIN 3" (SEQ ID No:115) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "IGF-ll MRNA-BINDING PROTEIN 3" encoded by a nucleic acid that hybridizes to the "IGF-ll MRNA-BINDING PROTEIN 3" nucleic acid or its complement under low stringency conditions, and/or

(ix) "MYB-BINDING PROTEIN 1A" (SEQ ID No:116) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "MYB-BINDING PROTEIN 1A" encoded by a nucleic acid that hybridizes to the "MYB- BINDING PROTEIN 1A" nucleic acid or its complement under low stringency conditions, and/or

(x) "NUCLEAR MATRIX PROTEIN NMP200" (SEQ ID No:117) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "NUCLEAR MATRIX PROTEIN NMP200" encoded by a nucleic acid that 256

hybridizes to the "NUCLEAR MATRIX PROTEIN NMP200" nucleic acid or its complement under low stringency conditions, and/or

(xi) "NUCLEOLAR PROTEIN NOP56" (SEQ ID No:118) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of

"NUCLEOLAR PROTEIN NOP56" encoded by a nucleic acid that hybridizes to the

"NUCLEOLAR PROTEIN NOP56" nucleic acid or its complement under low stringency conditions, and/or

(xii) "NUCLEOLAR RNA HELICASE II" (SEQ ID No:119) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "NUCLEOLAR RNA HELICASE II" encoded by a nucleic acid that hybridizes to the "NUCLEOLAR RNA HELICASE II" nucleic acid or its complement under low stringency conditions, and/or

(xiii) "NUCLEOPHOSMIN" (SEQ ID No:120) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of

"NUCLEOPHOSMIN" encoded by a nucleic acid that hybridizes to the

"NUCLEOPHOSMIN" nucleic acid or its complement under low stringency conditions, and/or

(xiv) "NUCLEOPLASMIN 3" (SEQ ID No:121) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of

"NUCLEOPLASMIN 3" encoded by a nucleic acid that hybridizes to the

"NUCLEOPLASMIN 3" nucleic acid or its complement under low stringency conditions, and/or

(xv) "POMBE CDC5-RELATED PROTEIN" (SEQ ID No:122) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "POMBE CDC5-RELATED PROTEIN" encoded by a nucleic acid that hybridizes to the "POMBE CDC5-RELATED PROTEIN" nucleic acid or its complement under low stringency conditions, and/or

P120" encoded by a nucleic acid that hybridizes to the "PROLIFERATING-CELL

NUCLEOLAR ANTIGEN P120" nucleic acid or its complement under low stringency conditions, and/or 257

(xvii) "RRP5 PROTEIN HOMOLOG (FRAGMENT)" (SEQ ID No:124) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "RRP5 PROTEIN HOMOLOG (FRAGMENT)" encoded by a nucleic acid that hybridizes to the "RRP5 PROTEIN HOMOLOG (FRAGMENT)" nucleic acid or its complement under low stringency conditions, and/or

(xviii) "Ringol " (SEQ ID No:125) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Ringol " encoded by a nucleic acid that hybridizes to the "Ringol " nucleic acid or its complement under low stringency conditions, and/or

(xix) "SIMILAR TO NUMB-ASSOCIATED KINASE" (SEQ ID No:126) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SIMILAR TO NUMB-ASSOCIATED KINASE" encoded by a nucleic acid that hybridizes to the "SIMILAR TO NUMB-ASSOCIATED KINASE" nucleic acid or its complement under low stringency conditions, and/or

(xx) "SIMILAR TO RIKEN CDNA 1110064N10 GENE" (SEQ ID No:127) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SIMILAR TO RIKEN CDNA 1110064N10 GENE" encoded by a nucleic acid that hybridizes to the "SIMILAR TO RIKEN CDNA 1110064N10 GENE" nucleic acid or its complement under low stringency conditions, and/or

(xxii) "cdk2" (SEQ ID No:129) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "cdk2" encoded by a nucleic acid that hybridizes to the "cdk2" nucleic acid or its complement under low stringency conditions, is present in the complex.

32. The method of any of No. 26 - 31 , wherein said method is a method of screening for a drug for treatment or prevention of a disease or disorder such as cancer such as breast cancer, lung cancer, colon cancer, prostate cancer, leukaemia;neurodegenerative diseases such as Alzheimer's disease and amyotrophic lateral sclerosis (ALS). 258

33. Use of a molecule that modulates the amount of, activity of, or the protein components of the complex of any one of No. 1 - 8 for the manufacture of a medicament for the treatment or prevention of a disease or disorder such as cancer such as breast cancer, lung cancer, colon cancer, prostate cancer, leukaemia;neurodegenerative diseases such as Alzheimer's disease and amyotrophic lateral sclerosis (ALS).

36. The method of No. 35, wherein the amount of said complex is determined.

37. The method of No. 35, wherein the activity of said complex is determined.

38. The method of No. 37, wherein said determining step comprises isolating from the subject said complex to produce said isolated complex and contacting said isolated complex in the presence or absence of a candidate molecule with a substrate of said complex and determining whether said substrate is processed in the absence of the candidate molecule and whether the processing of said substrate is modified in the presence of said candidate molecule. 259

40. The method of No. 39, wherein said determining step comprises determining whether (i) "BROMODOMAIN-CONTAINING PROTEIN 2" (SEQ ID No:108) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "BROMODOMAIN-CONTAINING PROTEIN 2" encoded by a nucleic acid that hybridizes to the "BROMODOMAIN-CONTAINING PROTEIN 2" nucleic acid or its complement under low stringency conditions, and/or

(iii) "CELL DIVISION PROTEIN KINASE 5" (SEQ ID No:110) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CELL DIVISION PROTEIN KINASE 5" encoded by a nucleic acid that hybridizes to the "CELL DIVISION PROTEIN KINASE 5" nucleic acid or its complement under low stringency conditions, and/or

(v) "HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN M, ISOFORM A" (SEQ ID No:112) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN M, ISOFORM A" encoded by a nucleic acid that hybridizes to the "HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN M, ISOFORM A" nucleic acid or its complement under low stringency conditions, and/or

(vi) "HYPOTHETICAL 24.3 KDA PROTEIN" (SEQ ID No:113) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYPOTHETICAL 24.3 KDA PROTEIN" encoded by a nucleic acid that 260

hybridizes to the "HYPOTHETICAL 24.3 KDA PROTEIN" nucleic acid or its complement under low stringency conditions, and/or

(x) "NUCLEAR MATRIX PROTEIN NMP200" (SEQ ID No:117) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "NUCLEAR MATRIX PROTEIN NMP200" encoded by a nucleic acid that hybridizes to the "NUCLEAR MATRIX PROTEIN NMP200" nucleic acid or its complement under low stringency conditions, and/or

(xi) "NUCLEOLAR PROTEIN NOP56" (SEQ ID No:118) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "NUCLEOLAR PROTEIN NOP56" encoded by a nucleic acid that hybridizes to the "NUCLEOLAR PROTEIN NOP56" nucleic acid or its complement under low stringency conditions, and/or

(xiii) "NUCLEOPHOSMIN" (SEQ ID No:120) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of 261

"NUCLEOPHOSMIN" encoded by a nucleic acid that hybridizes to the

"NUCLEOPLASMIN 3" encoded by a nucleic acid that hybridizes to the

P120" encoded by a nucleic acid that hybridizes to the "PROLIFERATING-CELL

NUCLEOLAR ANTIGEN P120" nucleic acid or its complement under low stringency conditions, and/or

(xix) "SIMILAR TO NUMB-ASSOCIATED KINASE" (SEQ ID No:126) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SIMILAR TO NUMB-ASSOCIATED KINASE" encoded by a nucleic acid that hybridizes to the "SIMILAR TO NUMB-ASSOCIATED KINASE" nucleic acid or its complement under low stringency conditions, and/or 262

41. The complex of any one of No. 1 - 8, or proteins of No. 13 or the antibody or fragment of No. 17, for use in a method of diagnosing a disease or disorder such as cancer such as breast cancer, lung cancer, colon cancer, prostate cancer, leukaemia;neurodegenerative diseases such as Alzheimer's disease and amyotrophic lateral sclerosis (ALS).

42. A method for treating or preventing a disease or disorder characterized by an aberrant amount of, activity or component composition of or intracellular localization of, the complex of anyone of No. 1 - 8, comprising administering to a subject in need of such treatment or prevention a therapeutically effective amount of one or more molecules that modulate the amount of, kinase activation, or protein components of, said complex.

45. Complex of any of No. 1 - 8 and/or protein selected from the following proteins 263

(iv) "DNA TOPOISOMERASE I" (SEQ ID No:111) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "DNA TOPOISOMERASE I" encoded by a nucleic acid that hybridizes to the "DNA TOPOISOMERASE I" nucleic acid or its complement under low stringency conditions, (v) "HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN M, ISOFORM A" (SEQ ID No: 112) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN M, ISOFORM A" encoded by a nucleic acid that hybridizes to the "HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN M, ISOFORM A" nucleic acid or its complement under low stringency conditions,

(vii) "HYPOTHETICAL PROTEIN XP_089560" (SEQ ID No:114) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYPOTHETICAL PROTEIN XP_089560" encoded by a nucleic acid that 264

hybridizes to the "HYPOTHETICAL PROTEIN XP_089560" nucleic acid or its complement under low stringency conditions,

(xiii) "NUCLEOPHOSMIN" (SEQ ID No:120) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "NUCLEOPHOSMIN" encoded by a nucleic acid that hybridizes to the "NUCLEOPHOSMIN" nucleic acid or its complement under low stringency conditions, (xiv) "NUCLEOPLASMIN 3" (SEQ ID No: 121) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "NUCLEOPLASMIN 3" encoded by a nucleic acid that hybridizes to the "NUCLEOPLASMIN 3" nucleic acid or its complement under low stringency conditions, 265

(xv) "POMBE CDC5-RELATED PROTEIN" (SEQ ID No: 122) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "POMBE CDC5-RELATED PROTEIN" encoded by a nucleic acid that hybridizes to the "POMBE CDC5-RELATED PROTEIN" nucleic acid or its complement under low stringency conditions,

P120" encoded by a nucleic acid that hybridizes to the "PROLIFERATING-CELL

(xxi) "cdc2" (SEQ ID No:128) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "cdc2" encoded by a nucleic acid that hybridizes to the "cdc2" nucleic acid or its complement under low stringency conditions, and/or(xxii) "cdk2" (SEQ ID No:129) or a functionally active 266

derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "cdk2" encoded by a nucleic acid that hybridizes to the "cdk2" nucleic acid or its complement under low stringency conditions,as a target for an active agent of a pharmaceutical, preferably a drug target in the treatment or prevention of a disease or disorder such as cancer such as breast cancer, lung cancer, colon cancer, prostate cancer, leukaemia;neurodegenerative diseases such as Alzheimer's disease and amyotrophic lateral sclerosis (ALS).

Thus, the invention further relates to the following embodiments of the Gab1 -signalling protein complex:

1. A protein complex selected from complex (I) and comprising (a) at least one first protein selected from the group consisting of: (i) "CRK" (SEQ ID No:137) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CRK" encoded by a nucleic acid that hybridizes to the "CRK" nucleic acid or its complement under low stringency conditions,

(ii) "ERK2" (SEQ ID No:138) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ERK2" encoded by a nucleic acid that hybridizes to the "ERK2" nucleic acid or its complement under low stringency conditions,

(iii) "GAB1 " (SEQ ID No:139) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "GAB1 " encoded by a nucleic acid that hybridizes to the "GAB1" nucleic acid or its complement under low stringency conditions,

(iv) "GRB2" (SEQ ID No:77) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "GRB2" encoded by a nucleic acid that hybridizes to the "GRB2" nucleic acid or its complement under low stringency conditions,

(v) "INOSITOL POLYPHOSPHATE 5-PHOSPHATASE" (SEQ ID No:141) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "INOSITOL POLYPHOSPHATE 5-PHOSPHATASE" encoded by a nucleic acid that hybridizes to the "INOSITOL POLYPHOSPHATE 5- PHOSPHATASE" nucleic acid or its complement under low stringency conditions, 267

(vi) "PI3-kinase" (SEQ ID No:147) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PI3-kinase" encoded by a nucleic acid that hybridizes to the "PI3-kinase" nucleic acid or its complement under low stringency conditions,

(vii) "PLC gamma" (SEQ ID No: 148) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PLC gamma" encoded by a nucleic acid that hybridizes to the "PLC gamma" nucleic acid or its complement under low stringency conditions,

(viii) "SHC" (SEQ ID No:96) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SHC" encoded by a nucleic acid that hybridizes to the "SHC" nucleic acid or its complement under low stringency conditions,

(ix) "SHIP" (SEQ ID No:150) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SHIP" encoded by a nucleic acid that hybridizes to the "SHIP" nucleic acid or its complement under low stringency conditions,

(x) "SHP2" (SEQ ID No:151) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SHP2" encoded by a nucleic acid that hybridizes to the "SHP2" nucleic acid or its complement under low stringency conditions, and

(xi) "c-Met (receptor)" (SEQ ID No:156) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "c-Met

(receptor)" encoded by a nucleic acid that hybridizes to the "c-Met (receptor)" nucleic acid or its complement under low stringency conditions, and

(xii) "c-CBL" (SEQ ID No:188) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "c-CBL" encoded by a nucleic acid that hybridizes to the "c-CBL" nucleic acid or its complement under low stringency conditions, and

(xiii) "IRS-1 " (SEQ ID No:189) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "IRS-1 " encoded by a nucleic acid that hybridizes to the "IRS-1" nucleic acid or its complement under low stringency conditions, and

(xiv) "IRS-2" (SEQ ID No:190) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "IRS-2" encoded by a 268 nucleic acid that hybridizes to the "IRS-2" nucleic acid or its complement under low stringency conditions, and

(i) "ABCC3" (SEQ ID No: 130) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ABCC3" encoded by a nucleic acid that hybridizes to the "ABCC3" nucleic acid or its complement under low stringency conditions,

(ii) "ACTIN-LIKE PROTEIN 3" (SEQ ID No:131) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ACTIN- LIKE PROTEIN 3" encoded by a nucleic acid that hybridizes to the "ACTIN-LIKE PROTEIN 3" nucleic acid or its complement under low stringency conditions, (iii) "ARP11 " (SEQ ID No:132) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ARP11" encoded by a nucleic acid that hybridizes to the "ARP11 " nucleic acid or its complement under low stringency conditions,

(iv) "ARP2/3 COMPLEX 34 KDA SUBUNIT" (SEQ ID No:133) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ARP2/3 COMPLEX 34 KDA SUBUNIT" encoded by a nucleic acid that hybridizes to the "ARP2/3 COMPLEX 34 KDA SUBUNIT" nucleic acid or its complement under low stringency conditions,

(v) "ARP3-BETA" (SEQ ID No:134) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ARP3-BETA" encoded by a nucleic acid that hybridizes to the "ARP3-BETA" nucleic acid or its complement under low stringency conditions,

(vi) "BCR1 " (SEQ ID No:135) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "BCR1" encoded by a nucleic acid that hybridizes to the "BCR1" nucleic acid or its complement under low stringency conditions,

(vii) "BCR2" (SEQ ID No:136) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "BCR2" encoded by a nucleic acid that hybridizes to the "BCR2" nucleic acid or its complement under low stringency conditions, 269

(viii) "HYP33.3KDA" (SEQ ID No: 140) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYP33.3KDA" encoded by a nucleic acid that hybridizes to the "HYP33.3KDA" nucleic acid or its complement under low stringency conditions,

(ix) "KIAA0729" (SEQ ID No:142) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA0729" encoded by a nucleic acid that hybridizes to the "KIAA0729" nucleic acid or its complement under low stringency conditions,

(x) "KIAA1529" (SEQ ID No: 143) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA1529" encoded by a nucleic acid that hybridizes to the "KIAA1529" nucleic acid or its complement under low stringency conditions,

(xi) "LOK" (SEQ ID No: 144) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "LOK" encoded by a nucleic acid that hybridizes to the "LOK" nucleic acid or its complement under low stringency conditions,

(xii) "MAD2L1 " (SEQ ID No:145) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "MAD2L1 " encoded by a nucleic acid that hybridizes to the "MAD2L1" nucleic acid or its complement under low stringency conditions,

(xiii) "P68 TRK-T3 ONCOPROTEIN" (SEQ ID No:146) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of

"P68 TRK-T3 ONCOPROTEIN" encoded by a nucleic acid that hybridizes to the "P68

TRK-T3 ONCOPROTEIN" nucleic acid or its complement under low stringency conditions,

(xiv) "PNAS-139 protein" (SEQ ID No:149) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PNAS-139 protein" encoded by a nucleic acid that hybridizes to the "PNAS-139 protein" nucleic acid or its complement under low stringency conditions,

(xv) "SIM2ARP3-BETA" (SEQ ID No:152) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SIM2ARP3-

BETA" encoded by a nucleic acid that hybridizes to the "SIM2ARP3-BETA" nucleic acid or its complement under low stringency conditions, 270

(xvi) "SIMI2RIKEN" (SEQ ID No:153) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SIMI2RIKEN" encoded by a nucleic acid that hybridizes to the "SIMI2RIKEN" nucleic acid or its complement under low stringency conditions,

(xvii) "ZFTF" (SEQ ID No:154) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ZFTF" encoded by a nucleic acid that hybridizes to the "ZFTF" nucleic acid or its complement under low stringency conditions, and

(xviii) "ZNF6-LIKE protein" (SEQ ID No:155) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ZNF6-LIKE protein" encoded by a nucleic acid that hybridizes to the "ZNF6-LIKE protein" nucleic acid or its complement under low stringency conditions, and a complex (II) comprising at least two of said second proteins, wherein said low stringency conditions comprise hybridization in a buffer comprising 35% formamide, 5X SSC, 50 mM Tris-HCI (pH 7.5), 5 mM EDTA, 0.02% PVP, 0.02% Ficoll, 0.2% BSA, 100 ug/ml denatured salmon sperm DNA, and 10% (wt/vol) dextran sulfate for 18-20 hours at 40 Celsius, washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4), 5 mM EDTA, and 0.1 % SDS for 1.5 hours at 55 Celsius, and washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4), 5 mM EDTA, and 0.1% SDS for 1.5 hours at 60 Celsius.

2. The protein complex according to No. 1 wherein the first protein is the protein Gab1 (SEQ ID NO. 139), or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of 'Gab1' encoded by a nucleic acid that hybridizes to the 'Gab1 ' under low stringency conditions.

(ii) "ACTIN-LIKE PROTEIN 3" (SEQ ID No:131) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ACTIN- 271

LIKE PROTEIN 3" encoded by a nucleic acid that hybridizes to the "ACTIN-LIKE

PROTEIN 3" nucleic acid or its complement under low stringency conditions,

(iii) "ARP11 " (SEQ ID No:132) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ARP11 " encoded by a nucleic acid that hybridizes to the "ARP11 " nucleic acid or its complement under low stringency conditions,

(vi) "BCR1 " (SEQ ID No:135) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "BCR1 " encoded by a nucleic acid that hybridizes to the "BCR1 " nucleic acid or its complement under low stringency conditions,

(vii) "BCR2" (SEQ ID No:136) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "BCR2" encoded by a nucleic acid that hybridizes to the "BCR2" nucleic acid or its complement under low stringency conditions,

(viii) "CRK" (SEQ ID No: 137) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CRK" encoded by a nucleic acid that hybridizes to the "CRK" nucleic acid or its complement under low stringency conditions,

(ix) "ERK2" (SEQ ID No:138) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ERK2" encoded by a nucleic acid that hybridizes to the "ERK2" nucleic acid or its complement under low stringency conditions,

(x) "GAB1 " (SEQ ID No:139) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "GAB1 " encoded by a 272

nucleic acid that hybridizes to the "GAB1 " nucleic acid or its complement under low stringency conditions,

(xi) "GRB2" (SEQ ID No:77) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "GRB2" encoded by a nucleic acid that hybridizes to the "GRB2" nucleic acid or its complement under low stringency conditions,

(xii) "HYP33.3KDA" (SEQ ID No:140) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYP33.3KDA" encoded by a nucleic acid that hybridizes to the "HYP33.3KDA" nucleic acid or its complement under low stringency conditions,

(xiii) "INOSITOL POLYPHOSPHATE 5-PHOSPHATASE" (SEQ ID No:141) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "INOSITOL POLYPHOSPHATE 5-PHOSPHATASE" encoded by a nucleic acid that hybridizes to the "INOSITOL POLYPHOSPHATE 5- PHOSPHATASE" nucleic acid or its complement under low stringency conditions, (xiv) "KIAA0729" (SEQ ID No:142) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA0729" encoded by a nucleic acid that hybridizes to the "KIAA0729" nucleic acid or its complement under low stringency conditions,

(xv) "KIAA1529" (SEQ ID No:143) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA1529" encoded by a nucleic acid that hybridizes to the "KIAA1529" nucleic acid or its complement under low stringency conditions,

(xvi) "LOK" (SEQ ID No: 144) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "LOK" encoded by a nucleic acid that hybridizes to the "LOK" nucleic acid or its complement under low stringency conditions,

(xvii) "MAD2L1 " (SEQ ID No:145) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "MAD2L1 " encoded by a nucleic acid that hybridizes to the "MAD2L1 " nucleic acid or its complement under low stringency conditions,

(xviii) "P68 TRK-T3 ONCOPROTEIN" (SEQ ID No: 146) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "P68 TRK-T3 ONCOPROTEIN" encoded by a nucleic acid that hybridizes to the "P68 273

(xix) "PI3-kinase" (SEQ ID No:147) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PI3-kinase" encoded by a nucleic acid that hybridizes to the "PI3-kinase" nucleic acid or its complement under low stringency conditions,

(xx) "PLC gamma" (SEQ ID No:148) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PLC gamma" encoded by a nucleic acid that hybridizes to the "PLC gamma" nucleic acid or its complement under low stringency conditions,

(xxi) "PNAS-139 protein" (SEQ ID No: 149) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PNAS-139 protein" encoded by a nucleic acid that hybridizes to the "PNAS-139 protein" nucleic acid or its complement under low stringency conditions,

(xxii) "SHC" (SEQ ID No:96) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SHC" encoded by a nucleic acid that hybridizes to the "SHC" nucleic acid or its complement under low stringency conditions,

(xxiii) "SHIP" (SEQ ID No:150) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SHIP" encoded by a nucleic acid that hybridizes to the "SHIP" nucleic acid or its complement under low stringency conditions,

(xxiv) "SHP2" (SEQ ID No:151) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SHP2" encoded by a nucleic acid that hybridizes to the "SHP2" nucleic acid or its complement under low stringency conditions,

(xxv) "SIM2ARP3-BETA" (SEQ ID No:152) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SIM2ARP3-

BETA" encoded by a nucleic acid that hybridizes to the "SIM2ARP3-BETA" nucleic acid or its complement under low stringency conditions,

(xxvi) "SIMI2RIKEN" (SEQ ID No: 153) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SIMI2RIKEN" encoded by a nucleic acid that hybridizes to the "SIMI2R1KEN" nucleic acid or its complement under low stringency conditions, 274

(xxvii) "ZFTF" (SEQ ID No:154) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ZFTF" encoded by a nucleic acid that hybridizes to the "ZFTF" nucleic acid or its complement under low stringency conditions,

(xxviii) "ZNF6-LIKE protein" (SEQ ID No: 155) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ZNF6- LIKE protein" encoded by a nucleic acid that hybridizes to the "ZNF6-LIKE protein" nucleic acid or its complement under low stringency conditions, and (xxix) "c-Met (receptor)" (SEQ ID No:156) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "c-Met (receptor)" encoded by a nucleic acid that hybridizes to the "c-Met (receptor)" nucleic acid or its complement under low stringency conditions, and

(xxx) "c-CBL" (SEQ ID No:188) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "c-CBL" encoded by a nucleic acid that hybridizes to the "c-CBL" nucleic acid or its complement under low stringency conditions, and

(xxxi) "IRS-1 " (SEQ ID No:189) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "IRS-1 " encoded by a nucleic acid that hybridizes to the "IRS-1 " nucleic acid or its complement under low stringency conditions, and

(xxxii) "IRS-2" (SEQ ID No:190) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "IRS-2" encoded by a nucleic acid that hybridizes to the "IRS-2" nucleic acid or its complement under low stringency conditions, and and a protein complex selected from complex (II) and comprising the following proteins: (i) "ABCC3" (SEQ ID No:130) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ABCC3" encoded by a nucleic acid that hybridizes to the "ABCC3" nucleic acid or its complement under low stringency conditions,

(ii) "ACTIN-LIKE PROTEIN 3" (SEQ ID No:131) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ACTIN- LIKE PROTEIN 3" encoded by a nucleic acid that hybridizes to the "ACTIN-LIKE PROTEIN 3" nucleic acid or its complement under low stringency conditions, 275

(iii) "ARP11" (SEQ ID No: 132) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ARP11 " encoded by a nucleic acid that hybridizes to the "ARP11 " nucleic acid or its complement under low stringency conditions,

(vii) "BCR2" (SEQ ID No: 136) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "BCR2" encoded by a nucleic acid that hybridizes to the "BCR2" nucleic acid or its complement under low stringency conditions,

(viii) "GAB1 " (SEQ ID No:139) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "GAB1 " encoded by a nucleic acid that hybridizes to the "GAB1 " nucleic acid or its complement under low stringency conditions,

(ix) "GRB2" (SEQ ID No:77) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "GRB2" encoded by a nucleic acid that hybridizes to the "GRB2" nucleic acid or its complement under low stringency conditions,

(x) "HYP33.3KDA" (SEQ ID No: 140) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYP33.3KDA" encoded by a nucleic acid that hybridizes to the "HYP33.3KDA" nucleic acid or its complement under low stringency conditions, 276

(xi) "INOSITOL POLYPHOSPHATE 5-PHOSPHATASE" (SEQ ID No:141) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "INOSITOL POLYPHOSPHATE 5-PHOSPHATASE" encoded by a nucleic acid that hybridizes to the "INOSITOL POLYPHOSPHATE 5-

PHOSPHATASE" nucleic acid or its complement under low stringency conditions,

(xii) "KIAA0729" (SEQ ID No: 142) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA0729" encoded by a nucleic acid that hybridizes to the "KIAA0729" nucleic acid or its complement under low stringency conditions,

(xiii) "KIAA1529" (SEQ ID No: 143) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA1529" encoded by a nucleic acid that hybridizes to the "KIAA1529" nucleic acid or its complement under low stringency conditions,

(xiv) "LOK" (SEQ ID No: 144) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "LOK" encoded by a nucleic acid that hybridizes to the "LOK" nucleic acid or its complement under low stringency conditions,

(xv) "MAD2L1 " (SEQ ID No:145) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "MAD2L1 " encoded by a nucleic acid that hybridizes to the "MAD2L1 " nucleic acid or its complement under low stringency conditions,

(xvi) "P68 TRK-T3 ONCOPROTEIN" (SEQ ID No:146) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of

"P68 TRK-T3 ONCOPROTEIN" encoded by a nucleic acid that hybridizes to the "P68

(xxvii) "Pl3-kinase" (SEQ ID No:147) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PI3-kinase" encoded by a nucleic acid that hybridizes to the "PI3-kinase" nucleic acid or its complement under low stringency conditions,

(xviii) "PLC gamma" (SEQ ID No: 148) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PLC gamma" encoded by a nucleic acid that hybridizes to the "PLC gamma" nucleic acid or its complement under low stringency conditions, 277

(xix) "PNAS-139 protein" (SEQ ID No:149) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PNAS-139 protein" encoded by a nucleic acid that hybridizes to the "PNAS-139 protein" nucleic acid or its complement under low stringency conditions,

(xx) "SHC" (SEQ ID No:96) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SHC" encoded by a nucleic acid that hybridizes to the "SHC" nucleic acid or its complement under low stringency conditions,

(xxi) "SHIP" (SEQ ID No:150) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SHIP" encoded by a nucleic acid that hybridizes to the "SHIP" nucleic acid or its complement under low stringency conditions,

(xxii) "SHP2" (SEQ ID No:151) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SHP2" encoded by a nucleic acid that hybridizes to the "SHP2" nucleic acid or its complement under low stringency conditions,

(xxiii) "SIM2ARP3-BETA" (SEQ ID No:152) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SIM2ARP3-

(xxiv) "SIMI2R1KEN" (SEQ ID No:153) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SIMI2RIKEN" encoded by a nucleic acid that hybridizes to the "S1MI2RIKEN" nucleic acid or its complement under low stringency conditions,

(xxv) "ZFTF" (SEQ ID No:154) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ZFTF" encoded by a nucleic acid that hybridizes to the "ZFTF" nucleic acid or its complement under low stringency conditions,

(xxvi) "ZNF6-LIKE protein" (SEQ ID No:155) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ZNF6-LIKE protein" encoded by a nucleic acid that hybridizes to the "ZNF6-L1KE protein" nucleic acid or its complement under low stringency conditions, and

(xxvii) "c-Met (receptor)" (SEQ ID No:156) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "c-Met 278

(receptor)" encoded by a nucleic acid that hybridizes to the "c-Met (receptor)" nucleic acid or its complement under low stringency conditions, and and a protein complex selected from complex (III) and comprising the following proteins:

(ii) "ACTIN-LIKE PROTEIN 3" (SEQ ID No:131) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ACTIN- LIKE PROTEIN 3" encoded by a nucleic acid that hybridizes to the "ACTIN-LIKE PROTEIN 3" nucleic acid or its complement under low stringency conditions, (iii) "ARP11 " (SEQ ID No:132) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ARP11 " encoded by a nucleic acid that hybridizes to the "ARP11 " nucleic acid or its complement under low stringency conditions,

(v) "ARP3-BETA" (SEQ ID No: 134) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ARP3-BETA" encoded by a nucleic acid that hybridizes to the "ARP3-BETA" nucleic acid or its complement under low stringency conditions,

(viii) "GAB1" (SEQ ID No:139) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "GAB1 " encoded by a 279

(x) "INOSITOL POLYPHOSPHATE 5-PHOSPHATASE" (SEQ ID No:141) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "INOSITOL POLYPHOSPHATE 5-PHOSPHATASE" encoded by a nucleic acid that hybridizes to the "INOSITOL POLYPHOSPHATE 5- PHOSPHATASE" nucleic acid or its complement under low stringency conditions,

(xi) "KIAA1529" (SEQ ID No: 143) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA1529" encoded by a nucleic acid that hybridizes to the "KIAA1529" nucleic acid or its complement under low stringency conditions,

(xii) "LOK" (SEQ ID No: 144) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "LOK" encoded by a nucleic acid that hybridizes to the "LOK" nucleic acid or its complement under low stringency conditions,

(xiii) "MAD2L1 " (SEQ ID No:145) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "MAD2L1 " encoded by a nucleic acid that hybridizes to the "MAD2L1 " nucleic acid or its complement under low stringency conditions,

(xiv) "PI3-kinase" (SEQ ID No: 147) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PI3-kinase" encoded by a nucleic acid that hybridizes to the "PI3-kinase" nucleic acid or its complement under low stringency conditions,

(xv) "PLC gamma" (SEQ ID No: 148) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PLC gamma" encoded by a nucleic acid that hybridizes to the "PLC gamma" nucleic acid or its complement under low stringency conditions,

(xvi) "SHC" (SEQ ID No:96) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SHC" encoded by a 280

nucleic acid that hybridizes to the "SHC" nucleic acid or its complement under low stringency conditions,

(xvii) "SHIP" (SEQ ID No: 150) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SHIP" encoded by a nucleic acid that hybridizes to the "SHIP" nucleic acid or its complement under low stringency conditions,

(xviii) "SHP2" (SEQ ID No:151) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SHP2" encoded by a nucleic acid that hybridizes to the "SHP2" nucleic acid or its complement under low stringency conditions,

(xix) "SIM2ARP3-BETA" (SEQ ID No:152) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SIM2ARP3- BETA" encoded by a nucleic acid that hybridizes to the "SIM2ARP3-BETA" nucleic acid or its complement under low stringency conditions,

(xx) "c-Met (receptor)" (SEQ ID No: 156) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "c-Met (receptor)" encoded by a nucleic acid that hybridizes to the "c-Met (receptor)" nucleic acid or its complement under low stringency conditions

4. The protein complex according to No. 1 comprising all but 1 - 19 of the following proteins:

(i) "ABCC3" (SEQ ID No:130) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ABCC3" encoded by a nucleic acid that hybridizes to the "ABCC3" nucleic acid or its complement under low stringency conditions,

(ii) "ACTIN-LIKE PROTEIN 3" (SEQ ID No:131) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ACTIN- LIKE PROTEIN 3" encoded by a nucleic acid that hybridizes to the "ACTIN-LIKE PROTEIN 3" nucleic acid or its complement under low stringency conditions, (iii) "ARP11 " (SEQ ID No:132) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ARP11" encoded by a nucleic acid that hybridizes to the "ARP11 " nucleic acid or its complement under low stringency conditions, 281

(x) "GAB1 " (SEQ ID No:139) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "GAB1 " encoded by a nucleic acid that hybridizes to the "GAB1 " nucleic acid or its complement under low stringency conditions,

(xi) "GRB2" (SEQ ID No:77) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "GRB2" encoded by a nucleic acid that hybridizes to the "GRB2" nucleic acid or its complement under low stringency conditions, 282

(xiii) "INOSITOL POLYPHOSPHATE 5-PHOSPHATASE" (SEQ ID No:141) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "INOSITOL POLYPHOSPHATE 5-PHOSPHATASE" encoded by a nucleic acid that hybridizes to the "INOSITOL POLYPHOSPHATE 5- PHOSPHATASE" nucleic acid or its complement under low stringency conditions, (xiv) "KIAA0729" (SEQ ID No: 142) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA0729" encoded by a nucleic acid that hybridizes to the "KIAA0729" nucleic acid or its complement under low stringency conditions,

(xv) "KIAA1529" (SEQ ID No: 143) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA1529" encoded by a nucleic acid that hybridizes to the "KIAA1529" nucleic acid or its complement under low stringency conditions,

(xvi) "LOK" (SEQ ID No:144) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "LOK" encoded by a nucleic acid that hybridizes to the "LOK" nucleic acid or its complement under low stringency conditions,

(xviii) "P68 TRK-T3 ONCOPROTEIN" (SEQ ID No:146) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "P68 TRK-T3 ONCOPROTEIN" encoded by a nucleic acid that hybridizes to the "P68 TRK-T3 ONCOPROTEIN" nucleic acid or its complement under low stringency conditions,

(xix) "PI3-kinase" (SEQ ID No:147) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PI3-kinase" encoded by a nucleic acid that hybridizes to the "PI3-kinase" nucleic acid or its complement under low stringency conditions, 283

(xx) "PLC gamma" (SEQ ID No: 148) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PLC gamma" encoded by a nucleic acid that hybridizes to the "PLC gamma" nucleic acid or its complement under low stringency conditions,

(xxi) "PNAS-139 protein" (SEQ ID No:149) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PNAS-139 protein" encoded by a nucleic acid that hybridizes to the "PNAS-139 protein" nucleic acid or its complement under low stringency conditions,

(xxvi) "SIMI2RIKEN" (SEQ ID No:153) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SIMI2RIKEN" encoded by a nucleic acid that hybridizes to the "SIMI2RIKEN" nucleic acid or its complement under low stringency conditions,

(xxviii) "ZNF6-LIKE protein" (SEQ ID No:155) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ZNF6- 284

LIKE protein" encoded by a nucleic acid that hybridizes to the "ZNF6-LIKE protein" nucleic acid or its complement under low stringency conditions,

(xxix) "c-Met (receptor)" (SEQ ID No: 156) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "c-Met

(receptor)" encoded by a nucleic acid that hybridizes to the "c-Met (receptor)" nucleic acid or its complement under low stringency conditions,

(xxxii) "IRS-2" (SEQ ID No:190) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "IRS-2" encoded by a nucleic acid that hybridizes to the "IRS-2" nucleic acid or its complement under low stringency conditions.

7. The complex of any of No. 1 - 4 comprising a fragment of said first protein and/or a fragment of said second protein, which fragment binds to another protein component of said complex. 285

8. The complex of any of No. 1 - 7 that is involved in the Cell motility acitvity, Focus forming activity, Tumorigenicity and experimental metastatic activity, In vitro invasion activity, Soft agar colony formation activity or Scatter activity.

12. Component of the Gab1 signaling complex obtainable by a process according to any of No. 9 - 11.

13. Protein of the Gab1 signaling complex selected from

(i) "HYP33.3KDA" (SEQ ID No: 140) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYP33.3KDA" encoded by a nucleic acid that hybridizes to the "HYP33.3KDA" nucleic acid or its complement under low stringency conditions,

(ii) "KIAA0729" (SEQ ID No:142) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA0729" encoded by a nucleic acid that hybridizes to the "KIAA0729" nucleic acid or its complement under low stringency conditions,

(iii) "K1AA1529" (SEQ ID No:143) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA1529" encoded by a nucleic acid that hybridizes to the "KIAA1529" nucleic acid or its complement under low stringency conditions, 286

(iv) "PNAS-139 protein" (SEQ ID No:149) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PNAS-139 protein" encoded by a nucleic acid that hybridizes to the "PNAS-139 protein" nucleic acid or its complement under low stringency conditions, and

(v) "SIMI2RIKEN" (SEQ ID No:153) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SIMI2RIKEN" encoded by a nucleic acid that hybridizes to the "SIMI2RIKEN" nucleic acid or its complement under low stringency conditions, wherein said low stringency conditions comprise hybridization in a buffer comprising 35% formamide, 5X SSC, 50 mM Tris-HCI (pH 7.5), 5 mM EDTA, 0.02% PVP, 0.02% Ficoll, 0.2% BSA, 100 ug/ml denatured salmon sperm DNA, and 10% (wt/vol) dextran sulfate for 18-20 hours at 40 Celsius, washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4), 5 mM EDTA, and 0.1 % SDS for 1.5 hours at 55 Celsius, and washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4), 5 mM EDTA, and 0.1% SDS for 1.5 hours at 60 Celsius.

14. Nucleic acid encoding a protein according to No. 13.

16. Host cell, containing a vector comprising at least one of the nucleic acid of No. 14 and/or a construct of No. 15 or containing several vectors each comprising at least the nucleic acid sequence encoding at least one of the proteins, or functionally active fragments or functionally active derivatives thereof selected from the first group of proteins according to No. 1 (a) and the proteins, or functionally active fragments or 287

19. The kit according to No. 18 for processing a substrate of said complex.

20. The kit according to No. 18 for the diagnosis or prognosis of a disease or a disease risk, preferentially for a disease or disorder such as metastatic cancer, proliferative disorder, psoriasis, .

(i) "HYP33.3KDA" (SEQ ID No:140) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYP33.3KDA" encoded by a nucleic acid that hybridizes to the "HYP33.3KDA" nucleic acid or its complement under low stringency conditions, 288

(iii) "KIAA1529" (SEQ ID No: 143) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA1529" encoded by a nucleic acid that hybridizes to the "KIAA1529" nucleic acid or its complement under low stringency conditions,

(iv) "PNAS-139 protein" (SEQ ID No:149) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PNAS-139 protein" encoded by a nucleic acid that hybridizes to the "PNAS-139 protein" nucleic acid or its complement under low stringency conditions, and/or

(v) "SIMI2RIKEN" (SEQ ID No:153) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SIMI2RIKEN" encoded by a nucleic acid that hybridizes to the "SIMI2RIKEN" nucleic acid or its complement under low stringency conditions, and a pharmaceutical acceptable carrier.

24. A pharmaceutical composition according to No. 23 for the treatment of diseases and disorders such as metastatic cancer, proliferative disorder, psoriasis, .

(i) "HYP33.3KDA" (SEQ ID No:140) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYP33.3KDA" encoded by a nucleic acid that hybridizes to the "HYP33.3KDA" nucleic acid or its complement under low stringency conditions,

(ii) "KIAA0729" (SEQ ID No: 142) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA0729" encoded by a nucleic acid that hybridizes to the "KIAA0729" nucleic acid or its complement under low stringency conditions,

(iii) "KIAA1529" (SEQ ID No: 143) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA1529" 289 encoded by a nucleic acid that hybridizes to the "KIAA1529" nucleic acid or its complement under low stringency conditions,

(v) "SIMI2RIKEN" (SEQ ID No:153) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SIMI2RIKEN" encoded by a nucleic acid that hybridizes to the "SIMI2RIKEN" nucleic acid or its complement under low stringency conditions, comprising the steps of

26. A method for screening for a molecule that modulates directly or indirectly the function, activity, composition or formation of the complex of any one of No. 1 - 8 comprising the steps of(a) exposing said complex, or a cell or organism containing Gab1 signaling complex to one or more candidate molecules; and

27. The method of No. 26, wherein the amount of said complex is determined.

28. The method of No. 26, wherein the activity of said complex is determined. 290

31. The method of No. 30, wherein said determining step comprises determining whether (i) "ABCC3" (SEQ ID No: 130) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ABCC3" encoded by a nucleic acid that hybridizes to the "ABCC3" nucleic acid or its complement under low stringency conditions, and/or

(ii) "ACTIN-LIKE PROTEIN 3" (SEQ ID No:131) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ACTIN- LIKE PROTEIN 3" encoded by a nucleic acid that hybridizes to the "ACTIN-LIKE PROTEIN 3" nucleic acid or its complement under low stringency conditions, and/or (iii) "ARP11 " (SEQ ID No:132) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ARP11 " encoded by a nucleic acid that hybridizes to the "ARP11 " nucleic acid or its complement under low stringency conditions, and/or

(iv) "ARP2/3 COMPLEX 34 KDA SUBUNIT" (SEQ ID No:133) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ARP2/3 COMPLEX 34 KDA SUBUNIT" encoded by a nucleic acid that hybridizes to the "ARP2/3 COMPLEX 34 KDA SUBUNIT" nucleic acid or its complement under low stringency conditions, and/or

(v) "ARP3-BETA" (SEQ ID No: 134) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ARP3-BETA" encoded by a nucleic acid that hybridizes to the "ARP3-BETA" nucleic acid or its complement under low stringency conditions, and/or

(vi) "BCR1 " (SEQ ID No:135) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "BCR1" encoded by a 291

nucleic acid that hybridizes to the "BCR1 " nucleic acid or its complement under low stringency conditions, and/or

(vii) "BCR2" (SEQ ID No: 136) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "BCR2" encoded by a nucleic acid that hybridizes to the "BCR2" nucleic acid or its complement under low stringency conditions, and/or

(viii) "CRK" (SEQ ID No: 137) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CRK" encoded by a nucleic acid that hybridizes to the "CRK" nucleic acid or its complement under low stringency conditions, and/or

(ix) "ERK2" (SEQ ID No: 138) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ERK2" encoded by a nucleic acid that hybridizes to the "ERK2" nucleic acid or its complement under low stringency conditions, and/or

(x) "GAB1 " (SEQ ID No:139) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "GAB1" encoded by a nucleic acid that hybridizes to the "GAB1" nucleic acid or its complement under low stringency conditions, and/or

(xi) "GRB2" (SEQ ID No:77) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "GRB2" encoded by a nucleic acid that hybridizes to the "GRB2" nucleic acid or its complement under low stringency conditions, and/or

(xiii) "HYP33.3KDA" (SEQ ID No:140) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYP33.3KDA" encoded by a nucleic acid that hybridizes to the "HYP33.3KDA" nucleic acid or its complement under low stringency conditions, and/or

(xiv) "INOSITOL POLYPHOSPHATE 5-PHOSPHATASE" (SEQ ID No:141) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "INOSITOL POLYPHOSPHATE 5-PHOSPHATASE" encoded by a nucleic acid that hybridizes to the "INOSITOL POLYPHOSPHATE 5-

PHOSPHATASE" nucleic acid or its complement under low stringency conditions, and/or

(xv) "KIAA0729" (SEQ ID No:142) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA0729" 292

encoded by a nucleic acid that hybridizes to the "KIAA0729" nucleic acid or its complement under low stringency conditions, and/or

(xvi) "KIAA1529" (SEQ ID No: 143) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA1529" encoded by a nucleic acid that hybridizes to the "KIAA1529" nucleic acid or its complement under low stringency conditions, and/or

(xvii) "LOK" (SEQ ID No:144) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "LOK" encoded by a nucleic acid that hybridizes to the "LOK" nucleic acid or its complement under low stringency conditions, and/or

(xviii) "MAD2L1 " (SEQ ID No:145) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "MAD2L1 " encoded by a nucleic acid that hybridizes to the "MAD2L1 " nucleic acid or its complement under low stringency conditions, and/or

(xix) "P68 TRK-T3 ONCOPROTEIN" (SEQ ID No:146) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of

"P68 TRK-T3 ONCOPROTEIN" encoded by a nucleic acid that hybridizes to the "P68

TRK-T3 ONCOPROTEIN" nucleic acid or its complement under low stringency conditions, and/or

(xx) "PI3-kinase" (SEQ ID No:147) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PI3-kinase" encoded by a nucleic acid that hybridizes to the "Pl3-kinase" nucleic acid or its complement under low stringency conditions, and/or

(xxi) "PLC gamma" (SEQ ID No: 148) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PLC gamma" encoded by a nucleic acid that hybridizes to the "PLC gamma" nucleic acid or its complement under low stringency conditions, and/or

(xxii) "PNAS-139 protein" (SEQ ID No: 149) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PNAS-139 protein" encoded by a nucleic acid that hybridizes to the "PNAS-139 protein" nucleic acid or its complement under low stringency conditions, and/or

(xxiii) "SHC" (SEQ ID No:96) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SHC" encoded by a 293

nucleic acid that hybridizes to the "SHC" nucleic acid or its complement under low stringency conditions, and/or

(xxiv) "SHIP" (SEQ ID No:150) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SHIP" encoded by a nucleic acid that hybridizes to the "SHIP" nucleic acid or its complement under low stringency conditions, and/or

(xxv) "SHP2" (SEQ ID No:151) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SHP2" encoded by a nucleic acid that hybridizes to the "SHP2" nucleic acid or its complement under low stringency conditions, and/or

(xxvi) "SIM2ARP3-BETA" (SEQ ID No:152) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SIM2ARP3-

BETA" encoded by a nucleic acid that hybridizes to the "SIM2ARP3-BETA" nucleic acid or its complement under low stringency conditions, and/or

(xxvii) "SIMI2RIKEN" (SEQ ID No:153) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "S1MI2RIKEN" encoded by a nucleic acid that hybridizes to the "SIMI2RIKEN" nucleic acid or its complement under low stringency conditions, and/or

(xxviii) "ZFTF" (SEQ ID No:154) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ZFTF" encoded by a nucleic acid that hybridizes to the "ZFTF" nucleic acid or its complement under low stringency conditions, and/or

(xxix) "ZNF6-LIKE protein" (SEQ ID No: 155) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ZNF6-LIKE protein" encoded by a nucleic acid that hybridizes to the "ZNF6-LIKE protein" nucleic acid or its complement under low stringency conditions, and/or

(xxx) "c-Met (receptor)" (SEQ ID No:156) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "c-Met

(receptor)" encoded by a nucleic acid that hybridizes to the "c-Met (receptor)" nucleic acid or its complement under low stringency conditions, and/or

(xxxi) "c-CBL" (SEQ ID No:188) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "c-CBL" encoded by a nucleic acid that hybridizes to the "c-CBL" nucleic acid or its complement under low stringency conditions, and/or 294

(xxxii) "IRS-1" (SEQ ID No:189) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "IRS-1 " encoded by a nucleic acid that hybridizes to the "IRS-1" nucleic acid or its complement under low stringency conditions, and/or

(xxxiii) "IRS-2" (SEQ ID No:190) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "IRS-2" encoded by a nucleic acid that hybridizes to the "IRS-2" nucleic acid or its complement under low stringency conditions, is present in the complex.

32. The method of any of No. 26 - 31 , wherein said method is a method of screening for a drug for treatment or prevention of a disease or disorder such as metastatic cancer, proliferative disorder, psoriasis, .

33. Use of a molecule that modulates the amount of, activity of, or the protein components of the complex of any one of No. 1 - 8 for the manufacture of a medicament for the treatment or prevention of a disease or disorder such as metastatic cancer, proliferative disorder, psoriasis, .

35. A method for diagnosing or screening for the presence of a disease or disorder or a predisposition for developing a disease or disorder in a subject, which disease or disorder is characterized by an aberrant amount of, activity of, or component composition of, or intracellular localization of the complex of any one of the No. 1 - 8, comprising determining the amount of, activity of, protein components of, and/or intracellular localization of, said complex and/or the transcription level of a gene dependent on the complex and/or the abundance and/or activity of a protein or protein complex dependent on the function of the complex and/or product of a gene dependent on the complex in a comparative sample derived from a subject, wherein a difference in said amount, activity, or protein components of, said complex in an analogous sample from a subject not 295

having the disease or disorder or predisposition indicates the presence in the subject of the disease or disorder or predisposition in the subject.

36. The method of No. 35, wherein the amount of said complex is determined.

37. The method of No. 35, wherein the activity of said complex is determined.

40. The method of No. 39, wherein said determining step comprises determining whether (i) "ABCC3" (SEQ ID No:130) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ABCC3" encoded by a nucleic acid that hybridizes to the "ABCC3" nucleic acid or its complement under low stringency conditions, and/or

(ii) "ACTIN-LIKE PROTEIN 3" (SEQ ID No:131) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ACTIN- LIKE PROTEIN 3" encoded by a nucleic acid that hybridizes to the "ACTIN-LIKE PROTEIN 3" nucleic acid or its complement under low stringency conditions, and/or (iii) "ARP11 " (SEQ ID No:132) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ARP11" encoded by a nucleic acid that hybridizes to the "ARP11 " nucleic acid or its complement under low stringency conditions, and/or

(iv) "ARP2/3 COMPLEX 34 KDA SUBUNIT" (SEQ ID No:133) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ARP2/3 COMPLEX 34 KDA SUBUNIT" encoded by a nucleic acid that 296

hybridizes to the "ARP2/3 COMPLEX 34 KDA SUBUNIT" nucleic acid or its complement under low stringency conditions, and/or

(v) "ARP3-BETA" (SEQ ID No:134) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ARP3-BETA" encoded by a nucleic acid that hybridizes to the "ARP3-BETA" nucleic acid or its complement under low stringency conditions, and/or

(vi) "BCR1" (SEQ ID No:135) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "BCR1" encoded by a nucleic acid that hybridizes to the "BCR1 " nucleic acid or its complement under low stringency conditions, and/or

(vii) "BCR2" (SEQ ID No:136) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "BCR2" encoded by a nucleic acid that hybridizes to the "BCR2" nucleic acid or its complement under low stringency conditions, and/or

(viii) "CRK" (SEQ ID No:137) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CRK" encoded by a nucleic acid that hybridizes to the "CRK" nucleic acid or its complement under low stringency conditions, and/or

(x) "GAB1" (SEQ ID No:139) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "GAB1" encoded by a nucleic acid that hybridizes to the "GAB1 " nucleic acid or its complement under low stringency conditions, and/or

(xiii) "HYP33.3KDA" (SEQ ID No: 140) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYP33.3KDA" encoded by a nucleic acid that hybridizes to the "HYP33.3KDA" nucleic acid or its complement under low stringency conditions, and/or 297

(xv) "KIAA0729" (SEQ ID No: 142) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA0729" encoded by a nucleic acid that hybridizes to the "KIAA0729" nucleic acid or its complement under low stringency conditions, and/or

(xvi) "KIAA1529" (SEQ ID No:143) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA1529" encoded by a nucleic acid that hybridizes to the "KIAA1529" nucleic acid or its complement under low stringency conditions, and/or

(xvii) "LOK" (SEQ ID No: 144) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "LOK" encoded by a nucleic acid that hybridizes to the "LOK" nucleic acid or its complement under low stringency conditions, and/or

(xviii) "MAD2L1 " (SEQ ID No:145) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "MAD2L1" encoded by a nucleic acid that hybridizes to the "MAD2L1" nucleic acid or its complement under low stringency conditions, and/or

(xix) "P68 TRK-T3 ONCOPROTEIN" (SEQ ID No: 146) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of

"P68 TRK-T3 ONCOPROTEIN" encoded by a nucleic acid that hybridizes to the "P68

(xx) "PI3-kinase" (SEQ ID No:147) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PI3-kinase" encoded by a nucleic acid that hybridizes to the "PI3-kinase" nucleic acid or its complement under low stringency conditions, and/or

(xxi) "PLC gamma" (SEQ ID No: 148) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PLC gamma" encoded by a nucleic acid that hybridizes to the "PLC gamma" nucleic acid or its complement under low stringency conditions, and/or 298

(xxiii) "SHC" (SEQ ID No:96) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SHC" encoded by a nucleic acid that hybridizes to the "SHC" nucleic acid or its complement under low stringency conditions, and/or

(xxv) "SHP2" (SEQ ID No: 151) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SHP2" encoded by a nucleic acid that hybridizes to the "SHP2" nucleic acid or its complement under low stringency conditions, and/or

(xxvii) "SIMI2RIKEN" (SEQ ID No:153) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SIMI2RIKEN" encoded by a nucleic acid that hybridizes to the "SIMI2RIKEN" nucleic acid or its complement under low stringency conditions, and/or

(xxix) "ZNF6-LIKE protein" (SEQ ID No:155) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ZNF6-LIKE protein" encoded by a nucleic acid that hybridizes to the "ZNF6-LIKE protein" nucleic acid or its complement under low stringency conditions, and/or

(xxx) "c-Met (receptor)" (SEQ ID No:156) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "c-Met 299

(xxxi) "c-CBL" (SEQ ID No:188) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "c-CBL" encoded by a nucleic acid that hybridizes to the "c-CBL" nucleic acid or its complement under low stringency conditions, and/or

(xxxii) "IRS-1 " (SEQ ID No:189) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "IRS-1 " encoded by a nucleic acid that hybridizes to the "IRS-1 " nucleic acid or its complement under low stringency conditions, and/or

41. The complex of any one of No. 1 - 8, or proteins of No. 13 or the antibody or fragment of No. 17, for use in a method of diagnosing a disease or disorder such as metastatic cancer, proliferative disorder, psoriasis, .

42. A method for treating or preventing a disease or disorder characterized by an aberrant amount of, activity or component composition of or intracellular localization of, the complex of anyone of No. 1 - 8, comprising administering to a subject in need of such treatment or prevention a therapeutically effective amount of one or more molecules that modulate the amount of, Cell motility acitvity, Focus forming activity, Tumorigenicity and experimental metastatic activity, In vitro invasion activity, Soft agar colony formation activity or Scatter activity, or protein components of, said complex.

44. The method according to No. 42 , wherein said disease or disorder involves increased levels of the amount or activity of said complex. 300

45. Complex of any of No. 1 - 8 and/or protein selected from the following proteins (i) "ABCC3" (SEQ ID No: 130) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ABCC3" encoded by a nucleic acid that hybridizes to the "ABCC3" nucleic acid or its complement under low stringency conditions,

(ii) "ACTIN-LIKE PROTEIN 3" (SEQ ID No: 131) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ACTIN- LIKE PROTEIN 3" encoded by a nucleic acid that hybridizes to the "ACTIN-LIKE PROTEIN 3" nucleic acid or its complement under low stringency conditions, (iii) "ARP11 " (SEQ ID No:132) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ARP11 " encoded by a nucleic acid that hybridizes to the "ARP11 " nucleic acid or its complement under low stringency conditions,

(viii) "CRK" (SEQ ID No: 137) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CRK" encoded by a 301

nucleic acid that hybridizes to the "CRK" nucleic acid or its complement under low stringency conditions,

(ix) "ERK2" (SEQ ID No: 138) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ERK2" encoded by a nucleic acid that hybridizes to the "ERK2" nucleic acid or its complement under low stringency conditions,

(xiii) "HYP33.3KDA" (SEQ ID No: 140) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYP33.3KDA" encoded by a nucleic acid that hybridizes to the "HYP33.3KDA" nucleic acid or its complement under low stringency conditions,

(xiv) "INOSITOL POLYPHOSPHATE 5-PHOSPHATASE" (SEQ ID No:141) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "INOSITOL POLYPHOSPHATE 5-PHOSPHATASE" encoded by a nucleic acid that hybridizes to the "INOSITOL POLYPHOSPHATE 5- PHOSPHATASE" nucleic acid or its complement under low stringency conditions, (xv) "KIAA0729" (SEQ ID No: 142) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA0729" encoded by a nucleic acid that hybridizes to the "K1AA0729" nucleic acid or its complement under low stringency conditions,

(xvi) "KIAA1529" (SEQ ID No:143) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA1529" encoded by a nucleic acid that hybridizes to the "KIAA1529" nucleic acid or its complement under low stringency conditions,

(xvii) "LOK" (SEQ ID No: 144) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "LOK" encoded by a nucleic 302

acid that hybridizes to the "LOK" nucleic acid or its complement under low stringency conditions,

(xviii) "MAD2L1" (SEQ ID No:145) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "MAD2L1 " encoded by a nucleic acid that hybridizes to the "MAD2L1 " nucleic acid or its complement under low stringency conditions,

"P68 TRK-T3 ONCOPROTEIN" encoded by a nucleic acid that hybridizes to the "P68

(xx) "PI3-kinase" (SEQ ID No: 147) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PI3-kinase" encoded by a nucleic acid that hybridizes to the "PI3-kinase" nucleic acid or its complement under low stringency conditions,

(xxi) "PLC gamma" (SEQ ID No:148) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PLC gamma" encoded by a nucleic acid that hybridizes to the "PLC gamma" nucleic acid or its complement under low stringency conditions,

(xxii) "PNAS-139 protein" (SEQ ID No: 149) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PNAS-139 protein" encoded by a nucleic acid that hybridizes to the "PNAS-139 protein" nucleic acid or its complement under low stringency conditions,

(xxiii) "SHC" (SEQ ID No:96) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SHC" encoded by a nucleic acid that hybridizes to the "SHC" nucleic acid or its complement under low stringency conditions,

(xxiv) "SHIP" (SEQ ID No:150) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SHIP" encoded by a nucleic acid that hybridizes to the "SHIP" nucleic acid or its complement under low stringency conditions,

(xxv) "SHP2" (SEQ ID No:151) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SHP2" encoded by a 303

nucleic acid that hybridizes to the "SHP2" nucleic acid or its complement under low stringency conditions,

(xxvii) "SIMI2RIKEN" (SEQ ID No:153) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SIMI2RIKEN" encoded by a nucleic acid that hybridizes to the "SIMI2RIKEN" nucleic acid or its complement under low stringency conditions,

(xxviii) "ZFTF" (SEQ ID No:154) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ZFTF" encoded by a nucleic acid that hybridizes to the "ZFTF" nucleic acid or its complement under low stringency conditions,

(xxix) "ZNF6-LIKE protein" (SEQ ID No:155) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ZNF6-LIKE protein" encoded by a nucleic acid that hybridizes to the "ZNF6-LIKE protein" nucleic acid or its complement under low stringency conditions,

(xxxi) "c-CBL" (SEQ ID No:188) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "c-CBL" encoded by a nucleic acid that hybridizes to the "c-CBL" nucleic acid or its complement under low stringency conditions, and

(xxxii) "IRS-1 " (SEQ ID No:189) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "IRS-1" encoded by a nucleic acid that hybridizes to the "IRS-1" nucleic acid or its complement under low stringency conditions, and

(xxxiii) "IRS-2" (SEQ ID No:190) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "IRS-2" encoded by a nucleic acid that hybridizes to the "IRS-2" nucleic acid or its complement under low stringency conditions, 304

as a target for an active agent of a pharmaceutical, preferably a drug target in the treatment or prevention of a disease or disorder such as metastatic cancer, proliferative disorder, psoriasis, .

Thus, the invention further relates to the following embodiments of the Bcl2-protein complex

1. A protein complex selected from complex (I) and comprising

(a) at least one first protein selected from the group consisting of:

(i) "ANT: Adenine Nucleotide Translocator" (SEQ ID No:157) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ANT: Adenine Nucleotide Translocator" encoded by a nucleic acid that hybridizes to the "ANT: Adenine Nucleotide Translocator" nucleic acid or its complement under low stringency conditions,

(ii) "Bad" (SEQ ID No: 159) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Bad" encoded by a nucleic acid that hybridizes to the "Bad" nucleic acid or its complement under low stringency conditions,

(iii) "Bax" (SEQ ID No: 160) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Bax" encoded by a nucleic acid that hybridizes to the "Bax" nucleic acid or its complement under low stringency conditions,

(iv) "Bcl-2" (SEQ ID No:161) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Bcl-2" encoded by a nucleic acid that hybridizes to the "Bcl-2" nucleic acid or its complement under low stringency conditions,

(v) "Bcl-2 interacting killer (Bik)" (SEQ ID No:162) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of

"Bcl-2 interacting killer (Bik)" encoded by a nucleic acid that hybridizes to the "Bcl-2 interacting killer (Bik)" nucleic acid or its complement under low stringency conditions,

(vi) "Bim" (SEQ ID No:163) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Bim" encoded by a nucleic 305

acid that hybridizes to the "Bim" nucleic acid or its complement under low stringency conditions, and

(vii) "PUMA" (SEQ ID No:173) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PUMA" encoded by a nucleic acid that hybridizes to the "PUMA" nucleic acid or its complement under low stringency conditions, and

(viii) "BAG1 " (SEQ ID No:191) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "BAG1 " encoded by a nucleic acid that hybridizes to the "BAG1 " nucleic acid or its complement under low stringency conditions,

(ix) "Harakiri" (SEQ ID No: 192) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Harakiri" encoded by a nucleic acid that hybridizes to the "Harakiri" nucleic acid or its complement under low stringency conditions,

(x) "Nip1 " (SEQ ID No:193) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Nip1" encoded by a nucleic acid that hybridizes to the "Nip1 " nucleic acid or its complement under low stringency conditions,

(xi) "Nip2" (SEQ ID No: 194) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Nip2" encoded by a nucleic acid that hybridizes to the "Nip2" nucleic acid or its complement under low stringency conditions,

(xii) "Nip3" (SEQ ID No:195) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Nip3" encoded by a nucleic acid that hybridizes to the "Nip3" nucleic acid or its complement under low stringency conditions,

(xiii) "Raf1 " (SEQ ID No:196) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Raf1" encoded by a nucleic acid that hybridizes to the "Raf1 " nucleic acid or its complement under low stringency conditions,

(xiv) "RRASP23" (SEQ ID No:197) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "RRASP23" encoded by a nucleic acid that hybridizes to the "RRASP23" nucleic acid or its complement under low stringency conditions, 306

(xv) "VDAC" (SEQ ID No:198) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "VDAC" encoded by a nucleic acid that hybridizes to the "VDAC" nucleic acid or its complement under low stringency conditions,

(i) "ATP-dependent DNA helicase II, 70 kDa subunit" (SEQ ID No: 158) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ATP-dependent DNA helicase II, 70 kDa subunit" encoded by a nucleic acid that hybridizes to the "ATP-dependent DNA helicase II, 70 kDa subunit" nucleic acid or its complement under low stringency conditions,

(ii) "CS BOX-CONTAINING WD PROTEIN" (SEQ ID No:164) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CS BOX-CONTAINING WD PROTEIN" encoded by a nucleic acid that hybridizes to the "CS BOX-CONTAINING WD PROTEIN" nucleic acid or its complement under low stringency conditions,

(iii) "DNA mismatch repair protein MLH3" (SEQ ID No:165) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "DNA mismatch repair protein MLH3" encoded by a nucleic acid that hybridizes to the "DNA mismatch repair protein MLH3" nucleic acid or its complement under low stringency conditions,

(iv) "GALECTIN-7" (SEQ ID No:166) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "GALECTIN-7" encoded by a nucleic acid that hybridizes to the "GALECTIN-7" nucleic acid or its complement under low stringency conditions,

(v) "GLUTAMINE SYNTHETASE" (SEQ ID No:167) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of

"GLUTAMINE SYNTHETASE" encoded by a nucleic acid that hybridizes to the

"GLUTAMINE SYNTHETASE" nucleic acid or its complement under low stringency conditions,

(vi) "HYPOTHETICAL 42.4 KDA PROTEIN" (SEQ ID No:168) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYPOTHETICAL 42.4 KDA PROTEIN" encoded by a nucleic acid that 307

hybridizes to the "HYPOTHETICAL 42.4 KDA PROTEIN" nucleic acid or its complement under low stringency conditions,

(vii) "Interleukin enhacer binding factor 3" (SEQ ID No:169) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Interleukin enhacer binding factor 3" encoded by a nucleic acid that hybridizes to the "Interleukin enhacer binding factor 3" nucleic acid or its complement under low stringency conditions,

(viii) "KIAA0894 PROTEIN" (SEQ ID No:170) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA0894 PROTEIN" encoded by a nucleic acid that hybridizes to the "KIAA0894 PROTEIN" nucleic acid or its complement under low stringency conditions,

(ix) "LEUKOCYTE ELASTASE INHIBITOR" (SEQ ID No:171) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "LEUKOCYTE ELASTASE INHIBITOR" encoded by a nucleic acid that hybridizes to the "LEUKOCYTE ELASTASE INHIBITOR" nucleic acid or its complement under low stringency conditions,

(x) "PROTEIN DISULFIDE ISOMERASE A6 PRECURSOR" (SEQ ID No:172) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PROTEIN DISULFIDE ISOMERASE A6 PRECURSOR" encoded by a nucleic acid that hybridizes to the "PROTEIN DISULFIDE ISOMERASE A6 PRECURSOR" nucleic acid or its complement under low stringency conditions, (xi) "SIMILAR TO PAI-1 MRNA-BINDING PROTEIN (H. SAPIENS)" (SEQ ID No:174) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SIMILAR TO PAI-1 MRNA-BINDING PROTEIN (H. SAPIENS)" encoded by a nucleic acid that hybridizes to the "SIMILAR TO PAI-1 MRNA- BINDING PROTEIN (H. SAPIENS)" nucleic acid or its complement under low stringency conditions,

(xii) "SQUAMOUS CELL CARCINOMA ANTIGEN 1" (SEQ ID No:46) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SQUAMOUS CELL CARCINOMA ANTIGEN 1 " encoded by a nucleic acid that hybridizes to the "SQUAMOUS CELL CARCINOMA ANTIGEN 1" nucleic acid or its complement under low stringency conditions,

(xiii) "SQUAMOUS CELL CARCINOMA ANTIGEN 2" (SEQ ID No:175) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, 308

or a variant of "SQUAMOUS CELL CARCINOMA ANTIGEN 2" encoded by a nucleic acid that hybridizes to the "SQUAMOUS CELL CARCINOMA ANTIGEN 2" nucleic acid or its complement under low stringency conditions,

(xiv) "Sodium-dependent neutral amino acid transporter" (SEQ ID No:176) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Sodium-dependent neutral amino acid transporter" encoded by a nucleic acid that hybridizes to the "Sodium-dependent neutral amino acid transporter" nucleic acid or its complement under low stringency conditions, (xv) "THYMIDINE PHOSPHORYLASE PRECURSOR" (SEQ ID No:177) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "THYMIDINE PHOSPHORYLASE PRECURSOR" encoded by a nucleic acid that hybridizes to the "THYMIDINE PHOSPHORYLASE PRECURSOR" nucleic acid or its complement under low stringency conditions,

(xvi) "TRANSCRIPTION FACTOR SUPT3H" (SEQ ID No:178) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TRANSCRIPTION FACTOR SUPT3H" encoded by a nucleic acid that hybridizes to the "TRANSCRIPTION FACTOR SUPT3H" nucleic acid or its complement under low stringency conditions,

(xvii) "WW DOMAIN-CONTAINING PROTEIN WWOX" (SEQ ID No:179) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "WW DOMAIN-CONTAINING PROTEIN WWOX" encoded by a nucleic acid that hybridizes to the "WW DOMAIN-CONTAINING PROTEIN WWOX" nucleic acid or its complement under low stringency conditions,

(xviii) "ZINC-ALPHA-2-GLYCOPROTEIN PRECURSOR" (SEQ ID No:180) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ZINC-ALPHA-2-GLYCOPROTEIN PRECURSOR" encoded by a nucleic acid that hybridizes to the "ZINC-ALPHA-2-GLYCOPROTEIN PRECURSOR" nucleic acid or its complement under low stringency conditions, and (xix) "large neutral amino acids transporter small subunit" (SEQ ID No:181) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "large neutral amino acids transporter small subunit" encoded by a nucleic acid that hybridizes to the "large neutral amino acids transporter small subunit" nucleic acid or its complement under low stringency conditions, 309

and a complex (II) comprising at least two of said second proteins, wherein said low stringency conditions comprise hybridization in a buffer comprising 35% formamide, 5X SSC, 50 mM Tris-HCI (pH 7.5), 5 mM EDTA, 0.02% PVP, 0.02% Ficoll, 0.2% BSA, 100 ug/ml denatured salmon sperm DNA, and 10% (wt/vol) dextran sulfate for 18-20 hours at 40 Celsius, washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4), 5 mM EDTA, and 0.1 % SDS for 1.5 hours at 55 Celsius, and washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4), 5 mM EDTA, and 0.1% SDS for 1.5 hours at 60 Celsius.

2. The protein complex according to No. 1 wherein the first protein is the protein Bcl-2 (SEQ ID NO. 4), or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of 'Bcl-2' encoded by a nucleic acid that hybridizes to the 'Bcl-2' under low stringency conditions.

(i) "ANT: Adenine Nucleotide Translocator" (SEQ ID No: 157) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ANT: Adenine Nucleotide Translocator" encoded by a nucleic acid that hybridizes to the "ANT: Adenine Nucleotide Translocator" nucleic acid or its complement under low stringency conditions,

(ii) "ATP-dependent DNA helicase II, 70 kDa subunit" (SEQ ID No:158) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ATP-dependent DNA helicase II, 70 kDa subunit" encoded by a nucleic acid that hybridizes to the "ATP-dependent DNA helicase II, 70 kDa subunit" nucleic acid or its complement under low stringency conditions,

(iii) "Bad" (SEQ ID No: 159) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Bad" encoded by a nucleic acid that hybridizes to the "Bad" nucleic acid or its complement under low stringency conditions,

(iv) "Bax" (SEQ ID No:160) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Bax" encoded by a nucleic acid that hybridizes to the "Bax" nucleic acid or its complement under low stringency conditions, 310

(v) "Bcl-2" (SEQ ID No: 161) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Bcl-2" encoded by a nucleic acid that hybridizes to the "Bcl-2" nucleic acid or its complement under low stringency conditions,

(vi) "Bcl-2 interacting killer (Bik)" (SEQ ID No:162) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of

(vii) "Bim" (SEQ ID No:163) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Bim" encoded by a nucleic acid that hybridizes to the "Bim" nucleic acid or its complement under low stringency conditions,

(viii) "CS BOX-CONTAINING WD PROTEIN" (SEQ ID No:164) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CS BOX-CONTAINING WD PROTEIN" encoded by a nucleic acid that hybridizes to the "CS BOX-CONTAINING WD PROTEIN" nucleic acid or its complement under low stringency conditions,

(ix) "DNA mismatch repair protein MLH3" (SEQ ID No:165) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "DNA mismatch repair protein MLH3" encoded by a nucleic acid that hybridizes to the "DNA mismatch repair protein MLH3" nucleic acid or its complement under low stringency conditions,

(x) "GALECTIN-7" (SEQ ID No:166) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "GALECTIN-7" encoded by a nucleic acid that hybridizes to the "GALECTIN-7" nucleic acid or its complement under low stringency conditions,

(xi) "GLUTAMINE SYNTHETASE" (SEQ ID No:167) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of

"GLUTAMINE SYNTHETASE" encoded by a nucleic acid that hybridizes to the

(xii) "HYPOTHETICAL 42.4 KDA PROTEIN" (SEQ ID No:168) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYPOTHETICAL 42.4 KDA PROTEIN" encoded by a nucleic acid that 311

(xiii) "Interleukin enhacer binding factor 3" (SEQ ID No:169) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Interleukin enhacer binding factor 3" encoded by a nucleic acid that hybridizes to the "Interleukin enhacer binding factor 3" nucleic acid or its complement under low stringency conditions,

(xiv) "KIAA0894 PROTEIN" (SEQ ID No:170) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA0894 PROTEIN" encoded by a nucleic acid that hybridizes to the "KIAA0894 PROTEIN" nucleic acid or its complement under low stringency conditions,

(xv) "LEUKOCYTE ELASTASE INHIBITOR" (SEQ ID No:171) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "LEUKOCYTE ELASTASE INHIBITOR" encoded by a nucleic acid that hybridizes to the "LEUKOCYTE ELASTASE INHIBITOR" nucleic acid or its complement under low stringency conditions,

(xvi) "PROTEIN DISULFIDE ISOMERASE A6 PRECURSOR" (SEQ ID No:172) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PROTEIN DISULFIDE ISOMERASE A6 PRECURSOR" encoded by a nucleic acid that hybridizes to the "PROTEIN DISULFIDE ISOMERASE A6 PRECURSOR" nucleic acid or its complement under low stringency conditions, (xvii) "PUMA" (SEQ ID No: 173) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PUMA" encoded by a nucleic acid that hybridizes to the "PUMA" nucleic acid or its complement under low stringency conditions,

(xviii) "SIMILAR TO PAI-1 MRNA-BINDING PROTEIN (H. SAPIENS)" (SEQ ID No:174) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SIMILAR TO PAI-1 MRNA-BINDING PROTEIN (H. SAPIENS)" encoded by a nucleic acid that hybridizes to the "SIMILAR TO PAI-1 MRNA- BINDING PROTEIN (H. SAPIENS)" nucleic acid or its complement under low stringency conditions,

(xix) "SQUAMOUS CELL CARCINOMA ANTIGEN 1 " (SEQ ID No:46) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SQUAMOUS CELL CARCINOMA ANTIGEN 1" encoded by a nucleic 312

acid that hybridizes to the "SQUAMOUS CELL CARCINOMA ANTIGEN 1" nucleic acid or its complement under low stringency conditions,

(xx) "SQUAMOUS CELL CARCINOMA ANTIGEN 2" (SEQ ID No:175) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SQUAMOUS CELL CARCINOMA ANTIGEN 2" encoded by a nucleic acid that hybridizes to the "SQUAMOUS CELL CARCINOMA ANTIGEN 2" nucleic acid or its complement under low stringency conditions,

(xxi) "Sodium-dependent neutral amino acid transporter" (SEQ ID No:176) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Sodium-dependent neutral amino acid transporter" encoded by a nucleic acid that hybridizes to the "Sodium-dependent neutral amino acid transporter" nucleic acid or its complement under low stringency conditions,

(xxii) "THYMIDINE PHOSPHORYLASE PRECURSOR" (SEQ ID No:177) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "THYMIDINE PHOSPHORYLASE PRECURSOR" encoded by a nucleic acid that hybridizes to the "THYMIDINE PHOSPHORYLASE

PRECURSOR" nucleic acid or its complement under low stringency conditions,

(xxiii) "TRANSCRIPTION FACTOR SUPT3H" (SEQ ID No:178) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TRANSCRIPTION FACTOR SUPT3H" encoded by a nucleic acid that hybridizes to the "TRANSCRIPTION FACTOR SUPT3H" nucleic acid or its complement under low stringency conditions,

(xxiv) "WW DOMAIN-CONTAINING PROTEIN WWOX" (SEQ ID No:179) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "WW DOMAIN-CONTAINING PROTEIN WWOX" encoded by a nucleic acid that hybridizes to the "WW DOMAIN-CONTAINING PROTEIN

WWOX" nucleic acid or its complement under low stringency conditions,

(xxv) "ZINC-ALPHA-2-GLYCOPROTEIN PRECURSOR" (SEQ ID No:180) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ZINC-ALPHA-2-GLYCOPROTElN PRECURSOR" encoded by a nucleic acid that hybridizes to the "ZINC-ALPHA-2-GLYCOPROTEIN

PRECURSOR" nucleic acid or its complement under low stringency conditions, and/or

(xxvi) "large neutral amino acids transporter small subunit" (SEQ ID No: 181) or a functionally active derivative thereof, or a functionally active fragment thereof, or a 313 homolog thereof, or a variant of "large neutral amino acids transporter small subunit" encoded by a nucleic acid that hybridizes to the "large neutral amino acids transporter small subunit" nucleic acid or its complement under low stringency conditions, (xxvii) "BAG1 " (SEQ ID No:191) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "BAG1" encoded by a nucleic acid that hybridizes to the "BAG1 " nucleic acid or its complement under low stringency conditions,

(xxviii) "Harakiri" (SEQ ID No:192) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Harakiri" encoded by a nucleic acid that hybridizes to the "Harakiri" nucleic acid or its complement under low stringency conditions,

(xxix) "Nip1 " (SEQ ID No:193) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Nip1 " encoded by a nucleic acid that hybridizes to the "Nip1 " nucleic acid or its complement under low stringency conditions,

(xxx) "Nip2" (SEQ ID No:194) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Nip2" encoded by a nucleic acid that hybridizes to the "Nip2" nucleic acid or its complement under low stringency conditions,

(xxxi) "Nip3" (SEQ ID No:195) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Nip3" encoded by a nucleic acid that hybridizes to the "Nip3" nucleic acid or its complement under low stringency conditions,

(xxxii) "Rafl" (SEQ ID No:196) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Rafl " encoded by a nucleic acid that hybridizes to the "Rafl " nucleic acid or its complement under low stringency conditions,

(xxxiii) "RRASP23" (SEQ ID No:197) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "RRASP23" encoded by a nucleic acid that hybridizes to the "RRASP23" nucleic acid or its complement under low stringency conditions,

(xxxiv) "VDAC" (SEQ ID No:198) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "VDAC" 314

encoded by a nucleic acid that hybridizes to the "VDAC" nucleic acid or its complement under low stringency conditions, and a protein complex selected from complex (II) and comprising the following proteins: (i) "ANT: Adenine Nucleotide Translocator" (SEQ ID No: 157) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ANT: Adenine Nucleotide Translocator" encoded by a nucleic acid that hybridizes to the "ANT: Adenine Nucleotide Translocator" nucleic acid or its complement under low stringency conditions,

(ii) "ATP-dependent DNA helicase II, 70 kDa subunit" (SEQ ID No:158) or a functionally active derivative thereof, or a functionally active ^"fragment thereof, or a homolog thereof, or a variant of "ATP-dependent DNA helicase II, 70 kDa subunit" encoded by a nucleic acid that hybridizes to the "ATP-dependent DNA helicase II, 70 kDa subunit" nucleic acid or its complement under low stringency conditions,

(iv) "Bax" (SEQ ID No: 160) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Bax" encoded by a nucleic acid that hybridizes to the "Bax" nucleic acid or its complement under low stringency conditions,

(v) "Bcl-2" (SEQ ID No:161) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Bcl-2" encoded by a nucleic acid that hybridizes to the "Bcl-2" nucleic acid or its complement under low stringency conditions,

(vi) "Bcl-2 interacting killer (Bik)" (SEQ ID No:162) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Bcl-2 interacting killer (Bik)" encoded by a nucleic acid that hybridizes to the "Bcl-2 interacting killer (Bik)" nucleic acid or its complement under low stringency conditions, (vii) "Bim" (SEQ ID No:163) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Bim" encoded by a nucleic acid that hybridizes to the "Bim" nucleic acid or its complement under low stringency conditions, 315

"GLUTAMINE SYNTHETASE" encoded by a nucleic acid that hybridizes to the

(xii) "HYPOTHETICAL 42.4 KDA PROTEIN" (SEQ ID No:168) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYPOTHETICAL 42.4 KDA PROTEIN" encoded by a nucleic acid that hybridizes to the "HYPOTHETICAL 42.4 KDA PROTEIN" nucleic acid or its complement under low stringency conditions,

(xiv) "KIAA0894 PROTEIN" (SEQ ID No:170) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA0894

PROTEIN" encoded by a nucleic acid that hybridizes to the "KIAA0894 PROTEIN" nucleic acid or its complement under low stringency conditions, 316

(xv) "LEUKOCYTE ELASTASE INHIBITOR" (SEQ ID No:171) or -a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "LEUKOCYTE ELASTASE INHIBITOR" encoded by a nucleic acid that hybridizes to the "LEUKOCYTE ELASTASE INHIBITOR" nucleic acid or its complement under low stringency conditions,

(xvi) "PROTEIN DISULFIDE ISOMERASE A6 PRECURSOR" (SEQ ID No:172) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PROTEIN DISULFIDE ISOMERASE A6 PRECURSOR" encoded by a nucleic acid that hybridizes to the "PROTEIN DISULFIDE ISOMERASE A6 PRECURSOR" nucleic acid or its complement under low stringency conditions, (xvii) "PUMA" (SEQ ID No:173) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PUMA" encoded by a nucleic acid that hybridizes to the "PUMA" nucleic acid or its complement under low stringency conditions,

(xix) "SQUAMOUS CELL CARCINOMA ANTIGEN 1 " (SEQ ID No:46) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SQUAMOUS CELL CARCINOMA ANTIGEN 1" encoded by a nucleic acid that hybridizes to the "SQUAMOUS CELL CARCINOMA ANTIGEN 1 " nucleic acid or its complement under low stringency conditions,

(xxi) "Sodium-dependent neutral amino acid transporter" (SEQ ID No: 176) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Sodium-dependent neutral amino acid transporter" 317

encoded by a nucleic acid that hybridizes to the "Sodium-dependent neutral amino acid transporter" nucleic acid or its complement under low stringency conditions, (xxii) "THYMIDINE PHOSPHORYLASE PRECURSOR" (SEQ ID No:177) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "THYMIDINE PHOSPHORYLASE PRECURSOR" encoded by a nucleic acid that hybridizes to the "THYMIDINE PHOSPHORYLASE PRECURSOR" nucleic acid or its complement under low stringency conditions, (xxiii) "TRANSCRIPTION FACTOR SUPT3H" (SEQ ID No:178) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TRANSCRIPTION FACTOR SUPT3H" encoded by a nucleic acid that hybridizes to the "TRANSCRIPTION FACTOR SUPT3H" nucleic acid or its complement under low stringency conditions,

(xxiv) "WW DOMAIN-CONTAINING PROTEIN WWOX" (SEQ ID No:179) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "WW DOMAIN-CONTAINING PROTEIN WWOX" encoded by a nucleic acid that hybridizes to the "WW DOMAIN-CONTAINING PROTEIN WWOX" nucleic acid or its complement under low stringency conditions, (xxv) "ZINC-ALPHA-2-GLYCOPROTEIN PRECURSOR" (SEQ ID No:180) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ZINC-ALPHA-2-GLYCOPROTEIN PRECURSOR" encoded by a nucleic acid that hybridizes to the "ZINC-ALPHA-2-GLYCOPROTEIN PRECURSOR" nucleic acid or its complement under low stringency conditions, and/or (xxvi) "large neutral amino acids transporter small subunit" (SEQ ID No: 181) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "large neutral amino acids transporter small subunit" encoded by a nucleic acid that hybridizes to the "large neutral amino acids transporter small subunit" nucleic acid or its complement under low stringency conditions, and a protein complex selected from complex (III) and comprising the following proteins: (i) "ANT: Adenine Nucleotide Translocator" (SEQ ID No:157) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ANT: Adenine Nucleotide Translocator" encoded by a nucleic acid that hybridizes to the "ANT: Adenine Nucleotide Translocator" nucleic acid or its complement under low stringency conditions, 318

(ii) "Bad" (SEQ ID No:159) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Bad" encoded by a nucleic acid that hybridizes to the "Bad" nucleic acid or its complement under low stringency conditions,

(iii) "Bax" (SEQ ID No:160) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Bax" encoded by a nucleic acid that hybridizes to the "Bax" nucleic acid or its complement under low stringency conditions,

(v) "Bcl-2 interacting killer (Bik)" (SEQ ID No:162) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Bcl-2 interacting killer (Bik)" encoded by a nucleic acid that hybridizes to the "Bcl-2 interacting killer (Bik)" nucleic acid or its complement under low stringency conditions, (vi) "Bim" (SEQ ID No:163) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Bim" encoded by a nucleic acid that hybridizes to the "Bim" nucleic acid or its complement under low stringency conditions,

(vii) "CS BOX-CONTAINING WD PROTEIN" (SEQ ID No:164) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CS BOX-CONTAINING WD PROTEIN" encoded by a nucleic acid that hybridizes to the "CS BOX-CONTAINING WD PROTEIN" nucleic acid or its complement under low stringency conditions,

(viii) "DNA mismatch repair protein MLH3" (SEQ ID No:165) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "DNA mismatch repair protein MLH3" encoded by a nucleic acid that hybridizes to the "DNA mismatch repair protein MLH3" nucleic acid or its complement under low stringency conditions,

(ix) "GALECTIN-7" (SEQ ID No:166) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "GALECTIN-7" encoded by a nucleic acid that hybridizes to the "GALECTIN-7" nucleic acid or its complement under low stringency conditions, 319

(x) "Interleukin enhacer binding factor 3" (SEQ ID No: 169) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Interleukin enhacer binding factor 3" encoded by a nucleic acid that hybridizes to the "Interleukin enhacer binding factor 3" nucleic acid or its complement under low stringency conditions,

(xi) "LEUKOCYTE ELASTASE INHIBITOR" (SEQ ID No:171) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "LEUKOCYTE ELASTASE INHIBITOR" encoded by a nucleic acid that hybridizes to the "LEUKOCYTE ELASTASE INHIBITOR" nucleic acid or its complement under low stringency conditions,

(xii) "PUMA" (SEQ ID No:173) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PUMA" encoded by a nucleic acid that hybridizes to the "PUMA" nucleic acid or its complement under low stringency conditions,

(xiii) "SQUAMOUS CELL CARCINOMA ANTIGEN 1 " (SEQ ID No:46) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SQUAMOUS CELL CARCINOMA ANTIGEN 1 " encoded by a nucleic acid that hybridizes to the "SQUAMOUS CELL CARCINOMA ANTIGEN 1" nucleic acid or its complement under low stringency conditions,

(xiv) "SQUAMOUS CELL CARCINOMA ANTIGEN 2" (SEQ ID No:175) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SQUAMOUS CELL CARCINOMA ANTIGEN 2" encoded by a nucleic acid that hybridizes to the "SQUAMOUS CELL CARCINOMA ANTIGEN 2" nucleic acid or its complement under low stringency conditions,

(xv) "Sodium-dependent neutral amino acid transporter" (SEQ ID No: 176) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Sodium-dependent neutral amino acid transporter" encoded by a nucleic acid that hybridizes to the "Sodium-dependent neutral amino acid transporter" nucleic acid or its complement under low stringency conditions,

(xvi) "WW DOMAIN-CONTAINING PROTEIN WWOX" (SEQ ID No:179) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "WW DOMAIN-CONTAINING PROTEIN WWOX" encoded by a nucleic acid that hybridizes to the "WW DOMAIN-CONTAINING PROTEIN WWOX" nucleic acid or its complement under low stringency conditions, 320

(xvii) "large neutral amino acids transporter small subunit" (SEQ ID No: 181) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "large neutral amino acids transporter small subunit" encoded by a nucleic acid that hybridizes to the "large neutral amino acids transporter small subunit" nucleic acid or its complement under low stringency conditions.

4. The protein complex according to No. 1 comprising all but 1 - 26 of the following proteins:

(ii) "ATP-dependent DNA helicase II, 70 kDa subunit" (SEQ ID No: 158) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ATP-dependent DNA helicase II, 70 kDa subunit" encoded by a nucleic acid that hybridizes to the "ATP-dependent DNA helicase II, 70 kDa subunit" nucleic acid or its complement under low stringency conditions,

(iii) "Bad" (SEQ ID No:159) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Bad" encoded by a nucleic acid that hybridizes to the "Bad" nucleic acid or its complement under low stringency conditions,

"Bcl-2 interacting killer (Bik)" encoded by a nucleic acid that hybridizes to the "Bcl-2 interacting killer (Bik)" nucleic acid or its complement under low stringency conditions, 321

"GLUTAMINE SYNTHETASE" encoded by a nucleic acid that hybridizes to the

(xiii) "Interleukin enhacer binding factor 3" (SEQ ID No:169) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Interleukin enhacer binding factor 3" encoded by a nucleic acid that hybridizes to the "Interleukin enhacer binding factor 3" nucleic acid or its complement under low stringency conditions, 322

(xix) "SQUAMOUS CELL CARCINOMA ANTIGEN 1" (SEQ ID No:46) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SQUAMOUS CELL CARCINOMA ANTIGEN 1 " encoded by a nucleic acid that hybridizes to the "SQUAMOUS CELL CARCINOMA ANTIGEN 1" nucleic acid or its complement under low stringency conditions,

(xx) "SQUAMOUS CELL CARCINOMA ANTIGEN 2" (SEQ ID No:175) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SQUAMOUS CELL CARCINOMA ANTIGEN 2" encoded by a nucleic acid that hybridizes to the "SQUAMOUS CELL CARCINOMA ANTIGEN 2" nucleic acid or its complement under low stringency conditions, 323

PRECURSOR" nucleic acid or its complement under low stringency conditions,

WWOX" nucleic acid or its complement under low stringency conditions,

(xxv) "ZINC-ALPHA-2-GLYCOPROTEIN PRECURSOR" (SEQ ID No:180) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ZINC-ALPHA-2-GLYCOPROTEIN PRECURSOR" encoded by a nucleic acid that hybridizes to the "ZINC-ALPHA-2-GLYCOPROTEIN

PRECURSOR" nucleic acid or its complement under low stringency conditions,

(xxvi) "large neutral amino acids transporter small subunit" (SEQ ID No:181) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "large neutral amino acids transporter small subunit" encoded by a nucleic acid that hybridizes to the "large neutral amino acids transporter small subunit" nucleic acid or its complement under low stringency conditions,

(xxvii) "BAG1 " (SEQ ID No: 191) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "BAG1" encoded by a nucleic acid that hybridizes to the "BAG1" nucleic acid or its complement under low stringency conditions, 324

(xxix) "Nip1 " (SEQ ID No:193) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Nip1" encoded by a nucleic acid that hybridizes to the "Nip1" nucleic acid or its complement under low stringency conditions,

(xxxii) "Raf 1 " (SEQ ID No:196) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Rafl " encoded by a nucleic acid that hybridizes to the "Rafl" nucleic acid or its complement under low stringency conditions,

(xxxiv) "VDAC" (SEQ ID No:198) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "VDAC" encoded by a nucleic acid that hybridizes to the "VDAC" nucleic acid or its complement under low stringency conditions.

5. The complex of any of No. 1 - 4 comprising a functionally active derivative of said first protein and/or a functionally active derivative of said second protein, wherein the functionally active derivative is a fusion protein comprising said first protein or said second protein fused to an amino acid sequence different from the first protein or second protein, respectively. 325

8. The complex of any of No. 1 - 7 that is involved in the Bcl-2 binding activity, cytochrome c release activity from mitochondria or apoptosis induction activity.

12. Component of the Bcl-2 complex obtainable by a process according to any of No. 9 - 11.

13. Protein of the Bcl-2 complex selected from

(i) "CS BOX-CONTAINING WD PROTEIN" (SEQ ID No: 164) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CS BOX-CONTAINING WD PROTEIN" encoded by a nucleic acid that hybridizes to the "CS BOX-CONTAINING WD PROTEIN" nucleic acid or its complement under low stringency conditions, and 326

(ii) "KIAA0894 PROTEIN" (SEQ ID No:170) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "K1AA0894 PROTEIN" encoded by a nucleic acid that hybridizes to the "KIAA0894 PROTEIN" nucleic acid or its complement under low stringency conditions, wherein said low stringency conditions comprise hybridization in a buffer comprising 35% formamide, 5X SSC, 50 mM Tris-HCI (pH 7.5), 5 mM EDTA, 0.02% PVP, 0.02% Ficoll, 0.2% BSA, 100 ug/ml denatured salmon sperm DNA, and 10% (wt/vol) dextran sulfate for 18-20 hours at 40 Celsius, washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4), 5 mM EDTA, and 0.1 % SDS for 1.5 hours at 55 Celsius, and washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4), 5 mM EDTA, and 0.1 % SDS for 1.5 hours at 60 Celsius.

14. Nucleic acid encoding a protein according to No. 13.

16. Host cell, containing a vector comprising at least one of the nucleic acid of No. 14 and/or a construct of No. 15 or containing several vectors each comprising at least the nucleic acid sequence encoding at least one of the proteins, or functionally active fragments or functionally active derivatives thereof selected from the first group of proteins according to No. 1 (a) and the proteins, or functionally active fragments or functionally active derivatives thereof selected from the second group of proteins according to No. 1 (b). 327

19. The kit according to No. 18 for processing a substrate of said complex.

20. The kit according to No. 18 for the diagnosis or prognosis of a disease or a disease risk, preferentially for a disease or disorder such as cancer such as solid tumours such as breast cancer, colorectal cancer, melanoma, prostate cancer and lung cancer;cancer such as hematological cancers such as lymphoma and myeloma.

(i) "CS BOX-CONTAINING WD PROTEIN" (SEQ ID No:164) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CS BOX-CONTAINING WD PROTEIN" encoded by a nucleic acid that hybridizes to the "CS BOX-CONTAINING WD PROTEIN" nucleic acid or its complement under low stringency conditions, and/or

(ii) "K1AA0894 PROTEIN" (SEQ ID No:170) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA0894 328

PROTEIN" encoded by a nucleic acid that hybridizes to the "KIAA0894 PROTEIN" nucleic acid or its complement under low stringency conditions, and a pharmaceutical acceptable carrier.

24. A pharmaceutical composition according to No. 23 for the treatment of diseases and disorders such as cancer such as solid tumours such as breast cancer, colorectal cancer, melanoma, prostate cancer and lung cancer;cancer such as hematological cancers such as lymphoma and myeloma.

(ii) "KIAA0894 PROTEIN" (SEQ ID No:170) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA0894 PROTEIN" encoded by a nucleic acid that hybridizes to the "KIAA0894 PROTEIN" nucleic acid or its complement under low stringency conditions, comprising the steps of

26. A method for screening for a molecule that modulates directly or indirectly the function, activity, composition or formation of the complex of any one of No. 1 - 8 comprising the steps of(a) exposing said complex, or a cell or organism containing Bcl-2 complex to one or more candidate molecules; and

(b) determining the amount of activity of protein components of, and/or intracellular localization of, said complex and/or the transcription level of a gene dependent on the complex and/or the abundance and/or activity of a protein or protein complex dependent 329

on the function of the complex and/or product of a gene dependent on the complex in the presence of the one or more candidate molecules, wherein a change in said amount, activity, protein components or intracellular localization relative to said amount, activity, protein components and/or intracellular localization and/or a change in the transcription level of a gene dependent on the complex and/or the abundance and/or activity of a protein or protein complex dependent on the function of the complex and/or product of a gene dependent on the complex in the absence of said candidate molecules indicates that the molecule modulates function, activity or composition of said complex.

27. The method of No. 26, wherein the amount of said complex is determined.

28. The method of No. 26, wherein the activity of said complex is determined.

31. The method of No. 30, wherein said determining step comprises determining whether (i) "ANT: Adenine Nucleotide Translocator" (SEQ ID No:157) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ANT: Adenine Nucleotide Translocator" encoded by a nucleic acid that hybridizes to the "ANT: Adenine Nucleotide Translocator" nucleic acid or its complement under low stringency conditions, and/or

(ii) "ATP-dependent DNA helicase II, 70 kDa subunit" (SEQ ID No:158) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ATP-dependent DNA helicase II, 70 kDa subunit" encoded by a nucleic acid that hybridizes to the "ATP-dependent DNA helicase II, 70 kDa subunit" nucleic acid or its complement under low stringency conditions, and/or 330

(iii) "Bad" (SEQ ID No:159) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Bad" encoded by a nucleic acid that hybridizes to the "Bad" nucleic acid or its complement under low stringency conditions, and/or

(iv) "Bax" (SEQ ID No: 160) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Bax" encoded by a nucleic acid that hybridizes to the "Bax" nucleic acid or its complement under low stringency conditions, and/or

(v) "Bcl-2" (SEQ ID No:161) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Bcl-2" encoded by a nucleic acid that hybridizes to the "Bcl-2" nucleic acid or its complement under low stringency conditions, and/or

"Bcl-2 interacting killer (Bik)" encoded by a nucleic acid that hybridizes to the "Bcl-2 interacting killer (Bik)" nucleic acid or its complement under low stringency conditions, and/or

(vii) "Bim" (SEQ ID No:163) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Bim" encoded by a nucleic acid that hybridizes to the "Bim" nucleic acid or its complement under low stringency conditions, and/or

(viii) "CS BOX-CONTAINING WD PROTEIN" (SEQ ID No:164) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "CS BOX-CONTAINING WD PROTEIN" encoded by a nucleic acid that hybridizes to the "CS BOX-CONTAINING WD PROTEIN" nucleic acid or its complement under low stringency conditions, and/or

(ix) "DNA mismatch repair protein MLH3" (SEQ ID No:165) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "DNA mismatch repair protein MLH3" encoded by a nucleic acid that hybridizes to the "DNA mismatch repair protein MLH3" nucleic acid or its complement under low stringency conditions, and/or

(x) "GALECTIN-7" (SEQ ID No:166) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "GALECTIN-7" 331

encoded by a nucleic acid that hybridizes to the "GALECTIN-7" nucleic acid or its complement under low stringency conditions, and/or

"GLUTAMINE SYNTHETASE" encoded by a nucleic acid that hybridizes to the

"GLUTAMINE SYNTHETASE" nucleic acid or its complement under low stringency conditions, and/or

(xii) "HYPOTHETICAL 42.4 KDA PROTEIN" (SEQ ID No:168) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "HYPOTHETICAL 42.4 KDA PROTEIN" encoded by a nucleic acid that hybridizes to the "HYPOTHETICAL 42.4 KDA PROTEIN" nucleic acid or its complement under low stringency conditions, and/or

(xiii) "Interleukin enhacer binding factor 3" (SEQ ID No:169) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Interieukin enhacer binding factor 3" encoded by a nucleic acid that hybridizes to the "Interleukin enhacer binding factor 3" nucleic acid or its complement under low stringency conditions, and/or

PROTEIN" encoded by a nucleic acid that hybridizes to the "K1AA0894 PROTEIN" nucleic acid or its complement under low stringency conditions, and/or

(xv) "LEUKOCYTE ELASTASE INHIBITOR" (SEQ ID No:171) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "LEUKOCYTE ELASTASE INHIBITOR" encoded by a nucleic acid that hybridizes to the "LEUKOCYTE ELASTASE INHIBITOR" nucleic acid or its complement under low stringency conditions, and/or

(xvi) "PROTEIN DISULFIDE ISOMERASE A6 PRECURSOR" (SEQ ID No:172) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PROTEIN DISULFIDE ISOMERASE A6 PRECURSOR" encoded by a nucleic acid that hybridizes to the "PROTEIN DISULFIDE ISOMERASE A6

(xvii) "PUMA" (SEQ ID No:173) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PUMA" 332

encoded by a nucleic acid that hybridizes to the "PUMA" nucleic acid or its complement under low stringency conditions, and/or

(xviii) "SIMILAR TO PAI-1 MRNA-BINDING PROTEIN (H. SAPIENS)" (SEQ ID No:174) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SIMILAR TO PAI-1 MRNA-BINDING PROTEIN (H. SAPIENS)" encoded by a nucleic acid that hybridizes to the "SIMILAR TO PAI-1 MRNA- BINDING PROTEIN (H. SAPIENS)" nucleic acid or its complement under low stringency conditions, and/or

(xix) "SQUAMOUS CELL CARCINOMA ANTIGEN 1 " (SEQ ID No:46) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SQUAMOUS CELL CARCINOMA ANTIGEN 1" encoded by a nucleic acid that hybridizes to the "SQUAMOUS CELL CARCINOMA ANTIGEN 1 " nucleic acid or its complement under low stringency conditions, and/or

(xx) "SQUAMOUS CELL CARCINOMA ANTIGEN 2" (SEQ ID No:175) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SQUAMOUS CELL CARCINOMA ANTIGEN 2" encoded by a nucleic acid that hybridizes to the "SQUAMOUS CELL CARCINOMA ANTIGEN 2" nucleic acid or its complement under low stringency conditions, and/or

(xxi) "Sodium-dependent neutral amino acid transporter" (SEQ ID No:176) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Sodium-dependent neutral amino acid transporter" encoded by a nucleic acid that hybridizes to the "Sodium-dependent neutral amino acid transporter" nucleic acid or its complement under low stringency conditions, and/or (xxii) "THYMIDINE PHOSPHORYLASE PRECURSOR" (SEQ ID No:177) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "THYMIDINE PHOSPHORYLASE PRECURSOR" encoded by a nucleic acid that hybridizes to the "THYMIDINE PHOSPHORYLASE PRECURSOR" nucleic acid or its complement under low stringency conditions, and/or (xxiii) "TRANSCRIPTION FACTOR SUPT3H" (SEQ ID No:178) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TRANSCRIPTION FACTOR SUPT3H" encoded by a nucleic acid that hybridizes to the "TRANSCRIPTION FACTOR SUPT3H" nucleic acid or its complement under low stringency conditions, and/or 333

(xxiv) "WW DOMAIN-CONTAINING PROTEIN WWOX" (SEQ ID No:179) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "WW DOMAIN-CONTAINING PROTEIN WWOX" encoded by a nucleic acid that hybridizes to the "WW DOMAIN-CONTAINING PROTEIN WWOX" nucleic acid or its complement under low stringency conditions, and/or (xxv) "ZINC-ALPHA-2-GLYCOPROTEIN PRECURSOR" (SEQ ID No:180) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ZINC-ALPHA-2-GLYCOPROTEIN PRECURSOR" encoded by a nucleic acid that hybridizes to the "ZINC-ALPHA-2-GLYCO PROTEIN PRECURSOR" nucleic acid or its complement under low stringency conditions, and/or (xxvi) "large neutral amino acids transporter small subunit" (SEQ ID No:181) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "large neutral amino acids transporter small subunit" encoded by a nucleic acid that hybridizes to the "large neutral amino acids transporter small subunit" nucleic acid or its complement under low stringency conditions, and/or (xxvii) "BAG1 " (SEQ ID No:191) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "BAG1" encoded by a nucleic acid that hybridizes to the "BAG1 " nucleic acid or its complement under low stringency conditions, and/or

(xxviii) "Harakiri" (SEQ ID No:192) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Harakiri" encoded by a nucleic acid that hybridizes to the "Harakiri" nucleic acid or its complement under low stringency conditions, and/or

(xxix) "Nip1 " (SEQ ID No:193) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Nip1 " encoded by a nucleic acid that hybridizes to the "Nip1 " nucleic acid or its complement under low stringency conditions, and/or

(xxx) "Nip2" (SEQ ID No:194) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Nip2" encoded by a nucleic acid that hybridizes to the "Nip2" nucleic acid or its complement under low stringency conditions, and/or

(xxxi) "Nip3" (SEQ ID No:195) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Nip3" encoded by a nucleic 334

acid that hybridizes to the "Nip3" nucleic acid or its complement under low stringency conditions, and/or

(xxxii) "Rafl " (SEQ ID No:196) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Rafl " encoded by a nucleic acid that hybridizes to the "Rafl" nucleic acid or its complement under low stringency conditions, and/or

(xxxiii) "RRASP23" (SEQ ID No:197) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "RRASP23" encoded by a nucleic acid that hybridizes to the "RRASP23" nucleic acid or its complement under low stringency conditions, and/or

(xxxiv) "VDAC" (SEQ ID No:198) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "VDAC" encoded by a nucleic acid that hybridizes to the "VDAC" nucleic acid or its complement under low stringency conditions, is present in the complex.

32. The method of any of No. 26 - 31 , wherein said method is a method of screening for a drug for treatment or prevention of a disease or disorder such as cancer such as solid tumours such as breast cancer, colorectal cancer, melanoma, prostate cancer and lung cancer;cancer such as hematological cancers such as lymphoma and myeloma.

33. Use of a molecule that modulates the amount of, activity of, or the protein components of the complex of any one of No. 1 - 8 for the manufacture of a medicament for the treatment or prevention of a disease or disorder such as cancer such as solid tumours such as breast cancer, colorectal cancer, melanoma, prostate cancer and lung cancer;cancer such as hematological cancers such as lymphoma and myeloma.

35. A method for diagnosing or screening for the presence of a disease or disorder or a predisposition for developing a disease or disorder in a subject, which disease or 335

disorder is characterized by an aberrant amount of, activity of, or component composition of, or intracellular localization of the complex of any one of the No. 1 - 8, comprising determining the amount of, activity of, protein components of, and/or intracellular localization of, said complex and/or the transcription level of a gene dependent on the complex and/or the abundance and/or activity of a protein or protein complex dependent on the function of the complex and/or product of a gene dependent on the complex in a comparative sample derived from a subject, wherein a difference in said amount, activity, or protein components of, said complex in an analogous sample from a subject not having the disease or disorder or predisposition indicates the presence in the subject of the disease or disorder or predisposition in the subject.

36. The method of No. 35, wherein the amount of said complex is determined.

37. The method of No. 35, wherein the activity of said complex is determined.

40. The method of No. 39, wherein said determining step comprises determining whether (i) "ANT: Adenine Nucleotide Translocator" (SEQ ID No:157) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ANT: Adenine Nucleotide Translocator" encoded by a nucleic acid that hybridizes to the "ANT: Adenine Nucleotide Translocator" nucleic acid or its complement under low stringency conditions, and/or

(ii) "ATP-dependent DNA helicase II, 70 kDa subunit" (SEQ ID No:158) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ATP-dependent DNA helicase II, 70 kDa subunit" encoded by a nucleic 336

acid that hybridizes to the "ATP-dependent DNA helicase II, 70 kDa subunit" nucleic acid or its complement under low stringency conditions, and/or

(iii) "Bad" (SEQ ID No: 159) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Bad" encoded by a nucleic acid that hybridizes to the "Bad" nucleic acid or its complement under low stringency conditions, and/or

(iv) "Bax" (SEQ ID No:160) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Bax" encoded by a nucleic acid that hybridizes to the "Bax" nucleic acid or its complement under low stringency conditions, and/or

(ix) "DNA mismatch repair protein MLH3" (SEQ ID No:165) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "DNA mismatch repair protein MLH3" encoded by a nucleic acid that hybridizes to the "DNA mismatch repair protein MLH3" nucleic acid or its complement under low stringency conditions, and/or 337

(x) "GALECTIN-7" (SEQ ID No:166) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "GALECTIN-7" encoded by a nucleic acid that hybridizes to the "GALECTIN-7" nucleic acid or its complement under low stringency conditions, and/or

"GLUTAMINE SYNTHETASE" encoded by a nucleic acid that hybridizes to the

(xiii) "Interleukin enhacer binding factor 3" (SEQ ID No:169) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Interleukin enhacer binding factor 3" encoded by a nucleic acid that hybridizes to the "Interleukin enhacer binding factor 3" nucleic acid or its complement under low stringency conditions, and/or

(xiv) "KIAA0894 PROTEIN" (SEQ ID No:170) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of. "KIAA0894

PROTEIN" encoded by a nucleic acid that hybridizes to the "KIAA0894 PROTEIN" nucleic acid or its complement under low stringency conditions, and/or

PRECURSOR" nucleic acid or its complement under low stringency conditions, and/or 338

(xvii) "PUMA" (SEQ ID No:173) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "PUMA" encoded by a nucleic acid that hybridizes to the "PUMA" nucleic acid or its complement under low stringency conditions, and/or

(xix) "SQUAMOUS CELL CARCINOMA ANTIGEN 1 " (SEQ ID No:46) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "SQUAMOUS CELL CARCINOMA ANTIGEN 1 " encoded by a nucleic acid that hybridizes to the "SQUAMOUS CELL CARCINOMA ANTIGEN 1" nucleic acid or its complement under low stringency conditions, and/or

(xxi) "Sodium-dependent neutral amino acid transporter" (SEQ ID No:176) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Sodium-dependent neutral amino acid transporter" encoded by a nucleic acid that hybridizes to the "Sodium-dependent neutral amino acid transporter" nucleic acid or its complement under low stringency conditions, and/or (xxii) ^" "THYMIDINE PHOSPHORYLASE PRECURSOR" (SEQ ID No:177) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "THYMIDINE PHOSPHORYLASE PRECURSOR" encoded by a nucleic acid that hybridizes to the "THYMIDINE PHOSPHORYLASE PRECURSOR" nucleic acid or its complement under low stringency conditions, and/or (xxiii) "TRANSCRIPTION FACTOR SUPT3H" (SEQ ID No:178) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "TRANSCRIPTION FACTOR SUPT3H" encoded by a nucleic acid that 339

hybridizes to the "TRANSCRIPTION FACTOR SUPT3H" nucleic acid or its complement under low stringency conditions, and/or

(xxiv) "WW DOMAIN-CONTAINING PROTEIN WWOX" (SEQ ID No: 179) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "WW DOMAIN-CONTAINING PROTEIN WWOX" encoded by a nucleic acid that hybridizes to the "WW DOMAIN-CONTAINING PROTEIN WWOX" nucleic acid or its complement under low stringency conditions, and/or (xxv) "ZINC-ALPHA-2-GLYCOPROTEIN PRECURSOR" (SEQ ID No:180) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "ZINC-ALPHA-2-GLYCOPROTEIN PRECURSOR" encoded by a nucleic acid that hybridizes to the "ZINC-ALPHA-2-GLYCOPROTEIN PRECURSOR" nucleic acid or its complement under low stringency conditions, and/or (xxvi) "large neutral amino acids transporter small subunit" (SEQ ID No:181) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "large neutral amino acids transporter small subunit" encoded by a nucleic acid that hybridizes to the "large neutral amino acids transporter small subunit" nucleic acid or its complement under low stringency conditions, and/or (xxvii) "BAG1 " (SEQ ID No:191) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "BAG1 " encoded by a nucleic acid that hybridizes to the "BAG1" nucleic acid or its complement under low stringency conditions, and/or

(xxix) "Nipl " (SEQ ID No:193) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Nipl" encoded by a nucleic acid that hybridizes to the "Nipl " nucleic acid or its complement under low stringency conditions, and/or

(xxx) "Nip2" (SEQ ID No:194) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Nip2" encoded by a nucleic acid that hybridizes to the "Nip2" nucleic acid or its complement under low stringency conditions, and/or 340

(xxxi) "Nip3" (SEQ ID No:195) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Nip3" encoded by a nucleic acid that hybridizes to the "Nip3" nucleic acid or its complement under low stringency conditions, and/or

(xxxii) "Rafl " (SEQ ID No:196) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Rafl " encoded by a nucleic acid that hybridizes to the "Rafl " nucleic acid or its complement under low stringency conditions, and/or

41. The complex of any one of No. 1 - 8, or proteins of No. 13 or the antibody or fragment of No. 17, for use in a method of diagnosing a disease or disorder such as cancer such as solid tumours such as breast cancer, colorectal cancer, melanoma, prostate cancer and lung cancer;cancer such as hematological cancers such as lymphoma and myeloma.

42. A method for treating or preventing a disease or disorder characterized by an aberrant amount of, activity or component composition of or intracellular localization of, the complex of anyone of No. 1 - 8, comprising administering to a subject in need of such treatment or prevention a therapeutically effective amount of one or more molecules that modulate the amount of, Bcl-2 binding activity, cytochrome c release activity from mitochondria or apoptosis induction activity, or protein components of, said complex.

43. The method according to No. 42, wherein said disease or disorder involves decreased levels of the amount or activity of said complex. 341

(iv) "Bax" (SEQ ID No:160) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Bax" encoded by a nucleic acid that hybridizes to the "Bax" nucleic acid or its complement under low stringency conditions,

"Bci-2 interacting killer (Bik)" encoded by a nucleic acid that hybridizes to the "Bcl-2 interacting killer (Bik)" nucleic acid or its complement under low stringency conditions,

(vii) "Bim" (SEQ ID No:163) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Bim" encoded by a nucleic 342

acid that hybridizes to the "Bim" nucleic acid or its complement under low stringency conditions,

(xi) "GLUTAMINE SYNTHETASE" (SEQ ID No: 167) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of

"GLUTAMINE SYNTHETASE" encoded by a nucleic acid that hybridizes to the

(xiv) "KIAA0894 PROTEIN" (SEQ ID No:170) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "KIAA0894 343

PROTEIN" encoded by a nucleic acid that hybridizes to the "K1AA0894 PROTEIN" nucleic acid or its complement under low stringency conditions,

(xxi) "Sodium-dependent neutral amino acid transporter" (SEQ ID No:176) or a functionally active derivative thereof, or a functionally active fragment thereof, or a 344

homolog thereof, or a variant of "Sodium-dependent neutral amino acid transporter" encoded by a nucleic acid that hybridizes to the "Sodium-dependent neutral amino acid transporter" nucleic acid or its complement under low stringency conditions,

PRECURSOR" nucleic acid or its complement under low stringency conditions,

WWOX" nucleic acid or its complement under low stringency conditions,

PRECURSOR" nucleic acid or its complement under low stringency conditions, and/or(xxvi) "large neutral amino acids transporter small subunit" (SEQ ID No:181) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "large neutral amino acids transporter small subunit" encoded by a nucleic acid that hybridizes to the "large neutral amino acids transporter small subunit" nucleic acid or its complement under low stringency conditions,

(xxvii) "BAG1" (SEQ ID No:191) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "BAG1" encoded by a nucleic acid that hybridizes to the "BAG1" nucleic acid or its complement under low stringency conditions,

(xxviii) "Harakiri" (SEQ ID No:192) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Harakiri" 345

encoded by a nucleic acid that hybridizes to the "Harakiri" nucleic acid or its complement under low stringency conditions,

(xxix) "Nipl" (SEQ ID No:193) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Nipl " encoded by a nucleic acid that hybridizes to the "Nipl " nucleic acid or its complement under low stringency conditions,

(xxxii) "Raf 1 " (SEQ ID No:196) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "Rafl" encoded by a nucleic acid that hybridizes to the "Rafl " nucleic acid or its complement under low stringency conditions,

(xxxiv) "VDAC" (SEQ ID No:198) or a functionally active derivative thereof, or a functionally active fragment thereof, or a homolog thereof, or a variant of "VDAC" encoded by a nucleic acid that hybridizes to the "VDAC" nucleic acid or its complement under low stringency conditions, as a target for an active agent of a pharmaceutical, preferably a drug target in the treatment or prevention of a disease or disorder such as cancer such as solid tumours such as breast cancer, colorectal cancer, melanoma, prostate cancer and lung cancer;cancer such as hematological cancers such as lymphoma and myeloma.

5. PROTOCOLS: 346

The TAP-technology, which is more fully describted in WO/0009716 and in Rigaut, G et.al. (1999), Nature Biotechnology. Vol 17 (10): 1030-1032 respectively was used and further adapted as described below for protein purification. Proteins were identified using Mass-spectrometry as described further below.

5.1 Construction of TAP-tagged bait

The cDNAs encoding the complete ORF were obtained by RT-PCR. Total RNA was prepared from appropriate cell lines using the RNeasy Mini Kit (Qiagen). Both cDNA synthesis and PCR were performed with the SUPERSCRIPT One-Step RT-PCR for Long templates Kit (Life Technologies) using gene-specific primers. After 35-40 cycles of amplification PCR-products with the expected size were gel-purified with the MinElute PCR Purification Kit (Qiagen) and, if necessary, used for further amplification. Low-abundant RNAs were amplified by nested PCR before gel-purification. Restriction sites for Notl were attached to PCR primers to allow subcloning of amplified cDNAs into the retroviral vectors plE94-N/C-TAP thereby generating N- or C-terminal fusions with the TAP-tag (Rigaut et al., 1999). Clones were analyzed by restriction digest, DNA sequencing and by in vitro translation using the TNT T7 Quick Coupled Transcription/Translation System (Promega inc.). The presence of the proteins was proven by Western blotting using the protein A part of the TAP-tag for detection. Briefly, separation of proteins by standard SDS-PAGE was followed by semi-dry transfer onto a nitrocellulose membrane (PROTRAN, Schleicher&Schuell) using the Multiphorll blotting apparatus from Pharmacia Biotech. The transfer buffer consisted of 48 mM Tris, 39 mM glycine, 10% methanol and 0,0375% sodium dodecylsulfate. After blocking in phosphate- buffered saline (PBS) supplemented with 10% dry milk powder and 0,1% Tween 20 transferred proteins were probed with the Peroxidase-Anti-Peroxidase Soluble Complex (Sigma) diluted in blocking solution. After intensive washing immunoreactive proteins were visualized by enhanced chemiluminescence (ECL; Amersham Pharmacia Biotech).

5.2 Preparation of Virus and infection

As a vector, a MoMLV-based recombinant virus was used. 347

The preparation has been carried out as follows:

5.2.1 Preparation of Virus

293 gp cells were grown to 100% confluency. They were split 1 :5 on poly-L-Lysine plates (1 :5 diluted Poly-L-Lysine [0.01% stock solution, Sigma P-4832] in PBS, left on plates for at least 10 min.)

On Day 2, 63 microgram of retroviral Vector DNA together with 13 microgram of DNA of plasmid encoding an appropriate envelope protein were transfected into 293 gp cells (Somia, NV et al (1999) Proc Natl Acad Scie USA 96: 12667-12672; Somia, NV et al (2000) J. Virol 74: 4420-4424)

On Day 3, the medium was replaced with 15 ml DMEM + 10% FBS per 15-cm dish.

On Day 4, the medium containing viruses (supernatant) was harvested (at 24 h following medium change after transfection). When a second collection was planned, DMEM 10 %

FBS was added to the plates and the plates were incubated for another 24 h.

All collections were done as follows:

The supernatant was filtered through 0.45 micrometer filter (Corning GmbH, cellulose acetate, 431155).

Filter was placed into konical polyallomer centrifuge tubes (Beckman, 358126) that are placed in buckets of a SW 28 rotor (Beckman).

The filtered supernatant was ultracentrifuged at 19400 rpm in the SW 28 rotor, for 2 hours at 21 degree Celsius. The supernatant was discarded. The pellet containing viruses was resuspended in a small volume (for example 300 microliter) of Hank's

Balanced Salt Solution [Gibco BRL, 14025-092], by pipetting up and down 100-times, using an aerosol-safe tip.

The viruses were used for transfection as described below.

5.2.2 Infection 348

Cells that were infected were plated one day before into one well of a 6-well plate. 4 hours before infection, the old medium on the cells was replaced with fresh medium. Only a minimal volume was added, so that the cells are completely covered (e.g. 700 microliter). During infection, the cells were actively dividing.

A description of the cells and their growth conditions is given in 5.2.3

To the concentrated virus, polybrene (Hexadimethrine Bromide; Sigma, H 9268) was added to achieve a final concentration of 8 microgram/ml (this is equivalent to 2.4 microliter of the 1 milligram/ml polybrene stock per 300 microliter of concentrated retrovirus). The virus was incubated in polybrene at room temperature for 1 hour.

For infection, the virus/polybrene mixture was added to the cells and incubated at 37 degree Celsius at the appropriate C0₂ concentration for several hours (e.g. over-day or over-night).

Following infection, the medium on the infected cells was replaced with fresh medium. The cells were passaged as usual after they became confluent. The cells contain the retrovirus integrated into their chromosomes and stably express the gene of interest.

5.2.3. Cell lines

For expression, Hek-293 cells (American Type Culture Collection-No. CRL-1573) were used. Cells were grown in 90% + 10% Fetal calf serum.

The expression pattern of the TAP-tagged protein was checked by immunoblot-analysis as described in 5.3.3 and/or by immunofluorescence as described in 5.3.1 or 5.3.2.

5.3 Checking of expression pattern of TAP-tagged proteins

The expression pattern of the TAP-tagged protein was checked by immunoblot-analysis and/or by immunofluorescence. 349

Immunofluorescence analysis was either carried out according to section 5.3.1 or to section 5.3.2 depending on the type of the TAP-tagged protein.

5.3.1. Protocol for the indirect Immunofluorescence staining of fixed mammalian cells for plasma membrane and ER bound proteins:

Cells were grown in FCS media on Polylysine coated 8 well chamber slides to 50% confluency. Then fixation of the cells was performed in 4% ParaFormAldehyde diluted in Phosphate Buffer Saline (PBS) solution (0.14M Phosphate, 0.1 M NaCI pH 7.4). The cells were incubated for 30 minutes at room temperature in 300 microliters per well. Quenching was performed in 0.1 M Glycine in PBS for 2x 20 minutes at room temperature. Blocking was performed with 1% Bovine Serum Albumin (BSA) in 0.3% Saponin + PBS for at least 1 hour at room temperature. Incubation of the primary antibodies was performed in the blocking solution overnight at +4 C. The proper dilution of the antibodies was determined in a case to case basis. Cells were washed in PBS containing 0.3% Saponin for 2x 20 minutes at room temperature. Incubation of the secondary antibodies is performed in the blocking solution. Alexa 594 coupled Goat anti- rabbit is diluted 1 :1000 (Molecular Probes). Alexa 488 coupled Goat anti-mouse is diluted 1 :1000 (Molecular Probes). DAPI was used to label DNA . If Phalloidin was used to label F-actin, the drug is diluted 1 :500 and incubated with the secondary antibodies. Cells were then washed again 2x20 minutes at room temperature in PBS. The excess of buffer was removed and cells were mounted in a media containing an anti-bleaching agent (Vectashield, Vector Laboratories).

5.3.2. Protocol for the indirect Immunofluorescence staining of fixed mammalian cells for non-plasma membrane bound proteins:

Cells were grown in FCS media on Polylysine coated 8 well chamber slides to 50% confluency. Fixation of the cells was performed in 4% ParaFormAldehyde diluted in Phosphate Buffer Saline (PBS) solution (0.14M Phosphate, 0.1 M NaCI pH 7.4) for 30 minutes at Room Temperature (ROOM TEMPERATURE), 300 microliters per well. Quenching was performed in 0.1 M Glycine in PBS for 2x 20 minutes at ROOM TEMPERATURE. Permeabilization of cells was done with 0.5% Triton X-100 in PBS for 350

10 minutes at room temperature. Blocking was then done in 1 % Bovine Serum Albumin (BSA) in 0.3% Saponin + PBS for at least 1 hour at ROOM TEMPERATURE (Blocking solution). Incubation of the primary antibodies was performed in the blocking solution, overnight at +4 C. The proper dilution of the antibodies has to be determined in a case to case basis. Cells were washed in PBS containing 0.3% Saponin, for 2x 20 minutes at ROOM TEMPERATURE. Incubation of the secondary antibodies was performed in the blocking solution. Alexa 594 coupled Goat anti-rabbit is diluted 1 :1000 (Molecular Probes), Alexa 488 coupled Goat anti-mouse is diluted 1 :1000 (Molecular Probes). DAPI was used to label DNA . If Phalloidin is used to label F-actin, the drug is diluted 1 :500 and incubated with the secondary antibodies. Cells were washed 2x 20 minutes at ROOM TEMPERATURE in PBS. The excess of buffer was removed and cells were mounted in a media containing an anti-bleaching agent (Vectashield, Vector Laboratories).

5.3.3 Immunoblot analysis

To analyze expression levels of TAP-tagged proteins, a cell pellet (from a 6-well dish) was lyzed in 60 μL DNAsel buffer (5% Glycerol, 100 mM NaCI, 0.8 % NP-40 (IGEPAL), 5 mM magnesium sulfate, 100 μg/ml DNAse I (Roche Diagnostics), 50 mM Tris, pH 7.5, protease inhibitor cocktail) for 15 min on ice.

Each sample was split into two aliquots. The first half was centrifuged at 13,000 rpm for 5 min. to yield the NP-40-extractable material in the supernatant; the second half (total material) was carefully triturated. 50 μg each of the NP-40-extractable material and the total material are mixed with DTT-containing sample buffer for 30 min at 50 oC on a shaker and separated by SDS polyacrylamide gel electrophoresis on a precast 4-12% Bis-Tris gel (Invitrogen).

Proteins were then transferred to nitrocellulose using a semi-dry procedure with a discontinuous buffer system. Briefly, gel and nitrocellulose membrane were stacked between filter papers soaked in either anode buffer (three layers buffer A1 (0.3 M Tris- HCI) and three layers buffer A2 (0.03 M Tris-HCI)) or cathode buffer (three layers of 0.03 M Tris-HCI, pH 9.4, 0.1 % SDS, 40 mM epsilon-aminocapronic acid). Electrotransfer of two gels at once was performed at 600 mA for 25 min.

Transferred proteins were visualized with Ponceau S solution for one min to control transfer efficiency and then destained in water. The membrane was blocked in 5% non- 351

fat milk powder in TBST (TBS containing 0.05% Tween-20) for 30 min at room temperature. It was subsequently incubated with HRP-coupled PAP antibody (1 :5000 diluted in 5% milk/TBST) for 1 h at room temperature, washed three times for 10 min in TBST. The blot membrane was finally soaked in chemiluminescent substrate (ECL, Roche Diagnostics) for 2 min. and either exposed to X-ray film or analyzed on an imaging station.

5.4. Purification or protein complexes

Depending on the type of the TAP-tagged proteins, purification was carried out using the appropriate protocol of the protocols below

5.4.1 Purification of cvtoplasmic proteins

For the purification of cytoplasmic TAP-tagged proteins 5 x 10⁸ adherent cells (corresponding to 40 15 cm plates) were used. The cells were harvested and washed 3 times in cold PBS (3 min, 1300 rpm, Heraeus centrifuge). The cells were frozen in liquid Nitrogen and stored at -80°C, or the TAP purification was directly continued. The cells were lysed in 10 ml CZ lysis buffer (50 mM Tris, pH 7.5, 5 % Glycerol, 0,2 % IGEPAL, 1.5 mM MgCI₂, 100 mM NaCI, 25 mM NaF, 1 mM Na3V04, 1 mM DTT, containing 1 tablet of Protease inhibitor cocktail (Roche) per 25 ml of buffer) by pipetting 2 times up and down, followed by a homogenizing step (10 strokes in a dounce homogenizer with tight pestle). The lysate was incubated for 30 min on ice. After spinning for 10 min at 20 OOOg, the supernatant was subjected to an ultracentrifugation step of 1 h at 100 000 g. The supernatant was frozen in liquid Nitrogen and stored at - 80°C, or the TAP purification was directly continued.

The lysates were thawn quickly in a 37°C waterbath. 0.4 ml of unsettled rabbit IgG- Agarose beads (Sigma, washed 3 times in CZ lysis buffer) were added, and incubated for 2 h rotating at 4°C. Protein complexes bound to the beads were obtained by centrifugation (1 min, 1300 rpm, Heraeus centrifuge). The beads were transferred into 0.8 ml Mobicol M1002 columns (Pierce) and washed with 10 ml CZ lysis buffer (containing 1 tablet of Protease inhibitor cocktail (Roche) per 50 ml of buffer). After an 352

additional washing step with 5 ml TEV cleavage buffer (10 mM Tris, pH 7.5, 100 mM NaCI, 0.1 % IGEPAL, 0.5 mM EDTA, 1 mM DTT), the protein-complexes were eluted from the beads by adding 150 μl TEV cleavage buffer, containing 5μl of TEV-protease (GibcoBRL, Cat.No. 10127-017). For better elution the columns were incubated at 160C for 1 h (shaking with 850 rpm). The eluate was applied on fresh Mobicol columns, containing 0.2 ml settled Calmodulin affinity resin (Stratagene, washed 3 times with CBP wash buffer). 0.2 ml 2 times CBP binding buffer (10 mM Tris, pH 7.5, 100 mM NaCI, 0,1 % IGEPAL, 2mM MgAc, 2mM Imidazole, 4 mM CaCI₂, 1 mM DTT) was added followed by an incubation of 1 h at 4°C, rotating. Protein-complexes bound to the Calmodulin affinity resin were washed with 10 ml of CBP wash buffer (10 mM Tris, pH 7.5, 100 mM NaCI, 0,1 % IGEPAL, 1mM MgAc, 1mM Imidazole, 2 mM CaCI₂, 1mM DTT). They were eluted by addition of 600 μl CBP elution buffer (10 mM Tris, pH 8.0, 5 mM EGTA) for 5 min at 37°C (shaking with 850 rpm). The eluates were transferred into a siliconized tube and lyophilised. The Calmodulin resin was boiled for 5 min in 50 μl 4x Laemmli sample buffer. The fractions were combined and applied on gradient NuPAGE gels (Invitrogen, 4-12%, 1.5 mm, 10 well).

5.4.2 Purification of membrane proteins

For the purification of membrane TAP-tagged proteins 5 x 10⁸ adherent cells (corresponding to 40 15 cm plates) were used. The cells were harvested and washed 3 times in cold PBS (3 min, 1300 rpm, Heraeus centrifuge). The cells were frozen in liquid Nitrogen and stored at -80°C, or the TAP purification was directly continued. The cells were lysed in 10 ml Membrane lysis buffer (50 mM Tris, pH 7.5, 7.5 % Glycerol, 1 mM EDTA, 150 mM NaCI, 25 mM NaF, 1 mM Na3V04, 1 mM DTT, containing 1 tablet of Protease inhibitor cocktail (Roche) per 25 ml of buffer) by pipetting 2 times up and down, followed by a homogenizing step (10 strokes in a dounce homogenizer with tight pestle). After spinning for 10 min at 1300 rpm (Heraeus centrifuge), the supernatant was subjected to an ultracentrifugation step of 1 h at 100 OOOg. The "Default" supernatant was frozen in liquid Nitrogen and stored at -80°C, or the TAP purification was directly continued. The "Membrane" pellet was resuspended in 7.5 ml Membrane lysis buffer (+ 0.8% IGEPAL) by pipetting, followed by resuspension through a gauge needle for 2 times. After incubation for 1 h at 4°C (rotating) the lysate was cleared by a centrifugation 353 step of 1 h at 100 000 g. The "Membrane" supernatant was frozen in liquid Nitrogen and stored at -80°C, or the TAP purification was directly continued.

The lysates were thawn quickly in a 37°C waterbath. 0.4 ml of unsettled rabbit IgG- Agarose beads (Sigma, washed 3 times in Membrane lysis buffer) were added, and incubated for 2 h rotating at 4°C. Protein complexes bound to the beads were obtained by centrifugation (1 min, 1300 rpm, Heraeus centrifuge). The beads were transferred into 0.8 ml Mobicol M1002 columns (Pierce) and the Membrane fractions were washed with 10 ml Membrane lysis buffer (containing 0.8% IGEPAL, and 1 tablet of Protease inhibitor cocktail (Roche) per 50 ml of buffer). The Default fractions were treated the same way, but the buffer was containing only 0.2% IGEPAL. After an additional washing step with 5 ml TEV cleavage buffer (10 mM Tris, pH 7.5, 100 mM NaCI, 0.5 mM EDTA, 1 mM DTT, containing 0.5% IGEPAL for the Membrane fraction and 0.1% IGEPAL for the Default fraction), the protein-complexes were eluted from the beads by adding 150 μl TEV cleavage buffer, containing 5μl of TEV-protease (GibcoBRL, Cat.No. 10127-017). For better elution the columns were incubated at 16°C for 1 h (shaking with 850 rpm). For the Membrane fraction 3 additional μl of TEV-protease were added and incubated for another hour. The eluate was applied on fresh Mobicol columns, containing 0.2 ml settled Calmodulin affinity resin (Stratagene, washed 3 times with CBP wash buffer). 0.2 ml 2 times CBP binding buffer (10 mM Tris, pH 7.5, 100 mM NaCI, 0,1 % IGEPAL, 2mM MgAc, 2mM Imidazole, 4 mM CaCI₂, 1mM DTT) was added followed by an incubation of 1 h at 4°C rotating. Protein-complexes bound to the Calmodulin affinity resin were washed with 10 ml of CBP wash buffer (10 mM Tris, pH 7.5, 100 mM NaCI, 0,1 % IGEPAL, 1 mM MgAc, 1mM Imidazole, 2 mM CaCI₂, 1mM DTT). They were eluted by addition of 600 μl CBP elution buffer (10 mM Tris, pH 8.0, 5 mM EGTA) for 5 min at 37°C (shaking with 850 rpm). The eluates were transferred into a siliconized tube and lyophilised. The Calmodulin resin was boiled for 5 min in 50 μl 4x Laemmli sample buffer. _f , The fractions were combined and applied on gradient NuPAGE gels (Invitrogen, 4-12%, 1.5 mm, 10 well).

5.4.3 Purification of nuclear proteins

For the purification of nuclear TAP-tagged proteins 5 x 10⁸ adherent cells (corresponding to 40 15 cm plates) were used. The cells were harvested and washed 3 times in cold 354

PBS (3 min, 1300 rpm, Heraeus centrifuge). The cells were frozen in liquid Nitrogen and stored at -80°C, or the TAP purification was directly continued.

The cells were lysed in 10 ml Hypotonic cell lysis buffer A (10 mM Tris, pH 7.5, 1.5 mM MgCI₂, 10 mM KCl, 25 mM NaF, 0.5 mM Na3V04, 1 mM DTT, containing 1 tablet of Protease inhibitor cocktail (Roche) per 25 ml of buffer) by pipetting 2 times up and incubation for 10 min on ice, followed by a homogenizing step (20 strokes in a dounce homogenizer with tight pestle). After spinning the lysate for 10 min at 2000g, "Default" supernatant and "Nuclear" pellet were treated separately. The Default fraction was made up to a final of 90 mM NaCI, 0,2 % NP40 and 5 % Glycerol. This was cleared by centrifugation for 1 h at 100 OOOg. The "Default" supernatant was frozen in liquid Nitrogen and stored at -80°C, or the TAP purification was directly continued. The Nuclear pellet was resuspended in 5 ml Nuclear lysis buffer B (50 mM Tris, pH 7.5, 1.5 mM MgCI₂, 20 % Glycerol, 420 mM NaCI, 25 mM NaF, 0.5 mM Na3V04, 1 mM DTT, containing 1 tablet of Protease inhibitor cocktail (Roche) per 25 ml of buffer) and incubated for 30 min on ice, shaking frequently. To precipitate the DNA Dilution buffer (50 mM Tris, pH 7.5, 0.26% IGEPAL, 1.5 mM MgCI₂, 25 mM NaF, 0.5 mM Na3V04, 1 mM DTT, containing 1 tablet of Protease inhibitor cocktail (Roche) per 50 ml of buffer) was added in a ratio of 1 :3 resuspended pellet to dilution buffer, and incubated for 10 more min on ice. After spinning for 1 h at 100 OOOg the supernatant was frozen in liquid Nitrogen and stored at -80°C, or the TAP purification was directly continued.

The lysates were thawn quickly in a 37°C waterbath. The Nuclear fractions were subjected to a centrifugation step of 20 min at 100 OOOg. 0.4 ml of unsettled rabbit IgG- Agarose beads (Sigma, washed 3 times in CZ lysis buffer) were added, and incubated for 2 h rotating at 4°C. Protein complexes bound to the beads were obtained by centrifugation (1 min, 1300 rpm, Heraeus centrifuge). The beads were transferred into 0.8 ml Mobicol M1002 columns (Pierce) and washed with 10 ml CZ lysis buffer (containing 1 tablet of Protease inhibitor cocktail (Roche) per 50 ml of buffer). After an additional washing step with 5 ml TEV cleavage buffer (10 mM Tris, pH 7.5, 100 mM NaCI, 0.1 % IGEPAL, 0.5 mM EDTA, 1 mM DTT), the protein-complexes were eluted from the beads by adding 150 μl TEV cleavage buffer, containing 5μl of TEV-protease (GibcoBRL, Cat. No. 10127-017). For better elution the columns were incubated at 160C for 1 h (shaking with 850 rpm). The eluate was applied on fresh Mobicol columns, containing 0.2 ml settled Calmodulin affinity resin (Stratagene, washed 3 times with CBP 355

wash buffer). 0.2 ml 2 times CBP binding buffer (10 mM Tris, pH 7.5, 100 mM NaCI, 0,1 % IGEPAL, 2mM MgAc, 2mM Imidazole, 4 mM CaCI2, 1 mM DTT) was added followed by an incubation of 1 h at 40C rotating. Protein-complexes bound to the Calmodulin affinity resin were washed with 10 ml of CBP wash buffer (10 mM Tris, pH 7.5, 100 mM NaCI, 0,1 % IGEPAL, 1mM MgAc, 1mM Imidazole, 2 mM CaCI₂, 1mM DTT). They were eluted by addition of 600 μl CBP elution buffer (10 mM Tris, pH 8.0, 5 mM EGTA) for 5 min at 37°C (shaking with 850 rpm). The eluates were transferred into a siliconized tube and lyophilised. The Calmodulin resin was boiled for 5 min in 50 μl 4x Laemmli sample buffer. The fractions were combined and applied on gradient NuPAGE gels (Invitrogen, 4-12%, 1.5 mm, 10 well).

5.5 Protein Identification by Mass Spectrometry

Protein Identification was carried out either by MALDI and/or by LC-MS/MS depending on the feasibility of the protocols for the individual tags. Both protocols are stated below.

5.5.1 Protein digestion prior to mass spectrometric analysis:

Gel-separated proteins were reduced, alkylated and digested in gel essentially following the procedure described by Shevchenko et al. (Shevchenko, A., Wilm, M., Vorm, O., Mann, M. Anal Chem 1996, 68, 850-858). Briefly, gel-separated proteins were excised from the gel using a clean scalpel, reduced using 10 mM DTT (in 5mM ammonium bicarbonate, 54 °C, 45 min) and subsequently alkylated with 55 mM iodoacetamid (in 5 mM ammonium bicarbonate) at room temperature in the dark (30 min). Reduced and alkylated proteins were digested in gel with porcine trypsin (Promega) at a protease concentration of 12.5 ng/μl in 5mM ammonium bicarbonate. Digestion was allowed to proceed for 4 hours at 37 °C and the reaction was subsequently stopped using 5 μl 5% formic acid.

5.5.2. Sample preparation prior to analysis by Mass-spectrometry 356

Depending on the MS-protocol used (see 5.5.3), samples were prepared either according to 5.5.2.1 or 5.5.2.2

5.5.2.1 Sample preparation prior to analysis bv MALDI TOF MS (matrix-assisted laser desorption/ionization time-of-flight mass spectrometry):

Peptides produced by in-gel digestion

Two μl of acidified digest supernatant were mixed with 2.5 μl 60% acetonitrile/0.1%TFA. Of that mixture, 1.5 μl were applied to a MALDI sample target plate and mixed with 2 μl of MALDI matrix (0.13mg/ml α-cyano-4-hydroxy cinnamic acid in 66%MeOH/33%Acetone). The sample was left to dry on the target followed by recrystallisation of the sample using 1 μl of 65% methanol/32% acetone/3% of a 0.1% TFA solution. Finally, the samples were washed once with a large volume of 0.1% TFA

5.5.2.2 Sample preparation prior to analysis bv LC-MS/MS (liquid chromatography coupled to tandem mass spectrometry)

Gel plugs were extracted twice with 20 μl 1 % TFA and pooled with acidified digest supernatants. Samples were dried in a a vaccum centrifuge and resuspended in 13 μl 1% TFA.

5.5.3. Mass-spectrometric data acquisition

As stated in the beginning of section 5.5, either the protocol stated in 5.5.3.1 or the protocol stated in 5.5.3.2 was used.

5.5.3.1. Mass spectrometric data acquisition bv MALDI TOF MS:

MALDI TOF mass spectra were acquired in delayed extraction mode on a Reflex III MALDI mass spectrometer (Bruker Daltonics) equipped with a 337 nm nitrogen laser. Several hundred spectra were averaged in order to produce acceptable signal to noise. Spectra were internally calibrated using standard peptides. The monoisotopic masses for all peptide ion signals detected in the acquired spectra were determined and used for database searching. 357

5.5.3.2 Mass spectrometric data acquisition bv LC-MS/MS:

Peptide samples were injected into a nano LC system (CapLC, Waters or Ultimate, Dionex) which was directly coupled either to a quadrupole TOF (QTOF2, QTOF Ultima, QTOF Micro, Micromass or QSTAR Pulsar, Sciex) or ion trap (LCQ Deca XP) mass spectrometer. Peptides were separated on the LC system using a gradient of aqueous and organic solvents (see below). Solvent A was 5% acetonitrile in 0.5% formic acid and solvent B was 70% acetonitrile in 0.5% formic acid.

mass spectrometer.

5.5.4 Protein identification

Depending on the MS-protocol used (see 5.5.3), proteins were identified either according to 5.5.4.1 or according to 5.5.4.2.

5.5.4.1. Protein identification using peptide mass fingerprinting (PMF):

The list of monoisotopic peptide masses obtained from a MALDI mass spectrum of a protein digest as produced in A was used to query fasta formatted protein sequence databases maintained and updated regularly at the NCBI (for the NCBInr) and European Bioinformatics Institute (EBI, for the human, mouse, Drosophila and C. Elegans proteome databases). Proteins were identified by peptide mass fingerprinting (Mann, M., Højrup, P., Roepstorff, P. Biol Mass Spectrom 1993, 22, 338-345; Pappin, D., Højrup, P, Bleasby, AJ Curr. Biol. 1993, 3, 327-33; Henzel, W. J., Billed, T. M., Stults, J. T., Wong, 358

S. C, Grimley, O, Watanabe, C. Proc Natl Acad Sci U S A 1993, 90, 5011-5015; Yates, J. R., Speicher, S., Griffin, P. R., Hunkapiller, T. Anal Biochem 1993, 214, 397-408; James, P., Quadroni, M., Carafoli, E., Gonnet, G. Biochem Biophys Res Commun 1993, 195, 58-64) using the software tool Profound (Proteometrics). In PMF, a protein is identified by correlating the measured peptide masses with the calculated peptide masses of a theoretical digest of all proteins present in the database. Search criteria included: tryptic protein cleavage, monoisotopic masses, 30 ppm mass accuracy. No restrictions on protein size or isoelectric point were imposed.

5.5.4.2 Protein identification using LC-MS/MS data:

The peptide mass and fragmentation data generated in the LC-MS/MS experiments were used to query fasta formatted protein and nucleotide sequence databases maintained and updated regularly at the NCBI (for the NCBInr, dbEST and the human and mouse genomes) and European Bioinformatics Institute (EBI, for the human, mouse, Drosophila and C. Elegans proteome databases). Proteins were identified by correlating the measured peptide mass and fragmentation data with the same data computed from the entries in the database using the software tool Mascot (Matrix Science, Perkins, D. N., Pappin, D. J., Creasy, D. M., Cottrell, J. S., Electrophoresis 1999, 20, 3551-67). Search criteria varied depending on which mass spectrometer was used for the analysis.

.5. 7 ASSAYS FOR ASSAYING THE ACTIVITIES OF THE COMPLEXES PRESENTED IN THE INVENTION

An exemplary Bcl-2 bindingassay can be carried out by contacting a complex having Bcl- 2 binding activity with immobilzed Bcl-2 protein substrate under appropriate conditions and detecting the bound protein partners. The detection of the bound protein partners can be carried out, e. g., using a specific antibody directed against the protein partner. The assay is a solid-phase binding assay with an enzyme-linked immunosorbent assay (ELISA) readout, where one member of the protein pair is attached to the surface of a polystyrene 96-well plate in a nonspecific manner. The second protein or interacting protein complex is incubated and allowed to bind to the first protein, and then is 359

specifically detected by a mouse monoclonal antibody. The readout for the assay is the colored product of a substrate converted by alkaline phosphatase enzyme, covalently conjugated to a second antibody, (see e.g. Diaz, JL (2000) Methods Enzymol 322: 255-66)

An exemplary assay to ascertain the transformation activity of a Gab1 -signalling protein complex provided herein can be carried out by expressing or inhibiting said complexes in a cell, plating said cells on soft agar in permissive media and fed said cells for a suitable period of time and monitor said cells for colonies of transformed cells. The colonies can be measured in terms of number and diameter to ascertain the transformation capability said complexes. An exemplary assay to detect transformation activity is described for example in Giordano S et al (1997) Proc Natl Acad Sci USA 94: 13868-72

An exemplary protein kinase assay can be carried out by contacting a complex having protein kinase activity with a suitable protein or peptide substrate and radioactivity [gamma 32P]-labelled ATP under appropriate conditions and detecting the amount of the phosphorylated protein substrate.

The detection of the phosphorylated protein substrate can be carried out, e.g., by filtrating the solution through a nitrocellulose filter and determining the radioactivity bound to the nitrocellulose filter (see e.g. Volonte C et al (1992) Biotechniques 12: 854-8, 860- 3)

An exemplary Cdk2 kinase activiation assay can be carried out by contacting a complex having Cdk2 kinase activation activity using ATP and GST-fused Cdk2 substrate under appropriate conditions followed by a histone H1 kinase assay and detecting the ability of

Cdk2 to phosphorylate histone H1.

The detection of phosphorylated histone H1 can be carried out, e. g., by separating the kinase reaction products by SDS-polyacrylamide gel electrophoresis followed by autoradiography.

(see e.g. Karaiskou A et al (2001) J Biol Chem 276: 36028)

An exemplary DNA binding assay can be carried out by contacting a complex having DNA binding activity with a radioactive [32P] end-labeled DNA substrate under appropriate conditions and detecting bound protein. 360

The detection of DNA bound protein can be carried out, e.g., by filtrating the solution through a nitrocellulose filter and determining the radioactivity bound to the filter (see e.g. Nowock J and Sippel AE (1982) Cell 30: 607-15).

This assay is based on the retention of nucleic acid-protein complexes on Nitrocellulose whereas free nucleic acid can pass through the filter.

TABLE 1

COMPOSITION OF COMPLEX

SQUAMOUS CELL SUPPRESSOR OF G2 CARCINOMA ANTIGEN 1 ALLELE OF SKP1 HOMOLOG

SUPPRESSOR OF G2 TELOMERASE-BINDING ALLELE OF SKP1 PROTEIN P23 HOMOLOG

TELOMERASE-BINDING TELOMERIC REPEAT PROTEIN P23 BINDING FACTOR 2

TELOMERIC REPEAT TERF1 (TRF1)- BINDING FACTOR 2 INTERACTING NUCLEAR FACTOR 2.

TERF1 (TRF1)- TRF1 INTERACTING NUCLEAR FACTOR 2.

TRF1 TRF2-INTERACTING TELOMERIC RAP1 PROTEIN.

TRF2-INTERACTING TRICARBOXYLATE TELOMERIC RAP1 TRANSPORT PROTEIN PROTEIN. MITOCHONDRIAL PRECURSOR

TRICARBOXYLATE U5 SMALL NUCLEAR TRANSPORT PROTEIN RIBONUCLEOPROTEIN MITOCHONDRIAL 200 KDA HELICASE PRECURSOR

PI3 KINASE VAV-3

REGULATORY SUBUNIT P85 ALPHA

PI3 KINASE WD-REPEAT PROTEIN 6.

REGULATORY SUBUNIT P85 BETA

PLC GAMMA WUGSC:H_RG122E10.2A

PROTEIN.

PROCOLLAGEN- PROLINE, 2- OXOGLUTARATE 4- DIOXYGENASE (PROLINE 4- HYDROXYLASE) ALPHA POLYPEPTIDE I.

RIBONUCLEOSIDE- DIPHOSPHATE REDUCTASE M2 CHAIN.

SEL-1 HOMOLOG PRECURSOR.

SHC

SIMILAR TO ADP.ATP CARRIER PROTEIN.

SIMILAR TO SIDEROFLEXIN 4.

SPHINGOSINE KINASE 2.

TRANSFERRIN RECEPTOR (P90, CD71).

BCR2 INOSITOL BCR2

POLYPHOSPHATE 5- PHOSPHATASE. c-CBL IRS-1 HYP33.3KDA

c-Met (receptor) IRS-2 KIAA0729

CRK PI3-kinase KIAA1529

ERK2 PLC gamma LOK

Gab1 SHC MAD2L1

GRB2 SHIP P68 TRK-T3 ONCOPROTEIN

HYP33.3KDA SHP2 PNAS-139 protein

INOSITOL SIM2ARP3-BETA.

POLYPHOSPHATE 5- PHOSPHATASE.

IRS-1 SIMI2RIKEN

IRS-2 ZFTF

KIAA0729 ZNF6-LIKE protein KIAA1529

TABLE 2

INDIVIDUAL PROTEINS

TABLE 3

BIOCHEMICAL ACTIVITIES OF THE COMPLEXES

TABLE 4

MEDICAL APPLICATION OF THE COMPLEX

396

The present invention is not to be limited in scope by the specific embodiments described herein. Indeed, various modifications of the invention in addition to those described herein will become apparent to those skilled in the art from the foregoing description and accompanying figures. Such modifications are intended to fall within the scope of the appended claims.

Various publications are cited herein, the disclosures of which are incorporated by reference in their entireties.

Claims

397CLAIMS

1. A protein complex selected from complex (I) and comprising

2. A protein complex comprising a first protein selected from the proteins listed in table 1 , fourth column of a given complex or a homologue or variant thereof, or a functionally active fragment or functionally active derivative of said first protein, the variant being encoded by a nucleic acid that hybridizes to the nucleic acid of said first protein under low stringency conditions, and at least one second protein selected from the group of proteins in table 1 , fifth column of a given complex, or a variant or homologue thereof, or a functionally active fragment or a functionally active derivative of said second protein, the variant of said second protein being encoded by a nucleic acid that hybridizes to the nucleic acid of said second protein under low- stringency conditions, and wherein said low stringency conditions comprise hybridization in a buffer comprising 35% formamide, 5X SSC, 50 mM Tris-HCI (pH 7.5), 5 mM EDTA, 0.02% PVP, 0.02% BSA, 100 ug/ml denatured salmon sperm 398

DNA, and 10% (wt/vol) dextran sulfate for 18-20 hours at 40°C, washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4), 5 mM EDTA, and 0.1% SDS for 1-5 hours at 55°C, and washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4) 5 mM EDTA, and 0.1% SDS for 1.5 hours at 60°C.

4. A protein complex that comprises all proteins as listed in table 1 , third column for a given complex or at least one protein being a homologue or a variant thereof, or a functionally active fragment or a functionally active derivative thereof, the variant being encoded by a nucleic acid that hybridizes to the nucleic acid of any of said proteins under low stringency conditions, except at least one protein of the proteins listed in table 5, third column, wherein said low stringency conditions comprise hybridization in a buffer comprising 35% formamide, 5X SSC, 50 mM Tris-HCI (pH 7.5), 5 mM EDTA, 0.02% PVP, 0.02% Ficoll, 0.2% BSA, 100 ug/ml denatured salmon sperm DNA, and 10% (wt/vol) dextran sulfate for 18-20 hours at 40°C, washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4), 5 mM EDTA, and 0.1 % SDS for 1-5 hours at 55°C, and washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4), 5 mM EDTA, and 0.1% SDS for 1.5 hours at 60°C, with the provisio that the complex comprises at least one protein selected from table 1, fifth column of a given complex. 399

5. The complex of any of Claim 1 - 4 comprising at least one functionally active derivative of said first protein and/or a functionally active derivative of said second protein, wherein the functionally active derivative is a fusion protein comprising said first protein or said second protein fused to an amino acid sequence different from the first protein or second protein.

6. The complex of Claim 5 wherein the functionally active derivative is a fusion protein comprising said first protein or said second protein fused to an affinity tag or label.

7. The complex of any of Claim 1 - 4 comprising a fragment of said first protein and/or a fragment of said second protein, which fragment binds to another protein component of said complex.

8. The complex of any of Claim 1 - 7 that is involved in at least one biochemical activity as stated in table 3.

9. A process for preparing a complex of any of Claim 1 - 8 and optionally the components thereof comprising the following steps: expressing a protein of the complex, preferably a tagged protein, in a target cell, or a tissue or an organ, isolating the protein complex which is attached to the protein, preferably the tagged protein, and optionally disassociating the protein complex and isolating the individual complex members.

10. The process according to Claim 9 wherein the tagged protein comprises two different tags which allow two separate affinity purification steps.

11. The process according to any of Claim 9 - 10 wherein the two tags are separated by a cleavage site for a protease.

12. Component of a protein complex obtainable by a process according to any of Claim 9 - 11.

13. Protein selected from the group of proteins in table 1 , sixth column of a given complex or a homologue or a variant of thereof, or a functionally active fragment or a 400

functionally active derivative of said protein, the variant being encoded by a nucleic acid that hybridizes to the nucleic acid encoding said protein under low stringency conditions, wherein said low stringency conditions comprise hybridization in a buffer comprising 35% formamide, 5X SSC, 50 mM Tris-HCI (pH 7.5), 5 mM EDTA, 0.02% PVP, 0.02% Ficoll, 0.2% BSA, 100 ug/ml denatured salmon sperm DNA, and 10% (wt/vol) dextran sulfate for 18-20 hours at 40°C, washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4), 5 mM EDTA, and 0.1 % SDS for 1.5 hours at 55°C, and washing in a buffer consisting of 2X SSC, 25 mM Tris-HCI (pH 7.4), 5 mM EDTA, and 0.1% SDS for 1.5 hours at 60°C.

14. Nucleic acid encoding a protein according to Claim 13.

15. Construct, preferably a vector construct, comprising

(a) a nucleic acid according to Claim 14 and at least one further nucleic acid which is normally not associated with said nucleic acid, or

(b) at least two separate nucleic acid sequences each encoding a different protein, or a functionally active fragment or a functionally active derivative thereof, or a homologue or a variant thereof, at least one of said proteins being selected from the first group of proteins according to Claim 1 (a) and at (east one of said proteins, being selected from the second group of proteins according to Claim 1 (b) or

(c) at least two separate nucleic acid sequences each encoding a different protein, or a functionally active fragment or a functionally active derivative thereof, or a homologue or a variant thereof, said proteins being selected from the proteins of complex (II) according to Claim 1.

16. Host cell, containing a vector comprising at least one nucleic acid of Claim 14 and /or a construct of Claim 15 or containing several vectors each comprising at least one nucleic acid encoding at least one protein selected from the first group of proteins according to Claim 1 (a) and at least one nucleic acid encoding at least one protein selected from the second group of proteins according to Claim 1 (b).

17. An antibody or a fragment of said antibody containing the binding domain thereof, selected from an antibody or fragment thereof, which binds the complex of any of 401

Claim 1 - 8 and which does not bind any of the proteins of said complex when uncomplexed and an antibody or a fragment of said antibody containing the binding domain thereof which binds to any of the proteins of the group of proteins according to Claim 13.

18. A kit comprising in one or more containers:

(a) the complex of any of Claim 1 - 8 and/or the proteins of Claim 13 and/or

(b) an antibody according to Claim 17 and/or

(c) a nucleic acid encoding a protein of the complex of any of Claim 1 - 8 and/or a protein of Claim 13 and/or

(d) cells expressing the complex of any of Claim 1 - 8 and/or a protein of Claim 13 and, optionally,

(e) further components such as reagents, buffers and working instructions.

19. The kit according to Claim 18 for processing a substrate of a complex of any one of Claim 1 - 8.

20. The kit according to Claim 18 for the diagnosis or prognosis of a disease or a disease risk, preferentially for a disease or disorder such as those as stated in column 2, table 4 of a given complex.

21. Array, preferably a microarray, in which at least a complex according to any of Claim 1 - 8 and/or at least one protein according to Claim 13 and/or at least one antibody according to Claim 17 is attached to a solid carrier.

22. A process for modifying a substrate of a complex of any one of Claim 1 - 8 comprising the step of bringing into contact a complex of any of Claim 1 - 8 with said substrate, such that said substrate is modified.

23. A pharmaceutical composition comprising the protein complex of any of Claim 1 - 8 and/or a protein according to Claim 13. 402

24. A pharmaceutical composition according to Claim 23 for the treatment of diseases and disorders, preferentially for diseases or disorders such as those as stated in column 2, table 4 of a given complex.

25. A method for screening for a molecule that binds to a complex of any one of Claim 1 - 8 and/or a protein of Claim 13, comprising the following steps:

26. A method for screening for a molecule that modulates directly or indirectly the function, activity, composition or formation of a complex of any one of Claim 1 - 8 comprising the steps of:

27. The method of Claim 26, wherein the amount of said complex is determined.

28. The method of Claim 26, wherein the activity of said complex is determined. 403

29. The method of Claim 28, wherein said determining step comprises isolating from the cell or organism said complex to produce said isolated complex and contacting said isolated complex in the presence or absence of a candidate molecule with a substrate of said complex and determining whether said substrate is processed in the absence of the candidate molecule and whether the processing of said substrate is modified in the presence of said candidate molecule.

30. The method of Claim 26, wherein the amount of the individual protein components of said complex is determined.

31. The method of Claim 30, wherein said determining step comprises determining whether any of the proteins listed in table 1 , third column of said complex, or a functionally active fragment or a functionally active derivative thereof, or a variant or a homologue thereof, the variant being encoded by a nucleic acid that hybridizes to the nucleic acid of said protein under low-stringency conditions, is present in the complex.

32. The method of any of Claim 26 - 31 , wherein said method is a method of screening for a drug for treatment or prevention of a disease or disorder, preferentially of a disease or disorder selected from the diseases or disorders such as those as stated in column 2, table 4 of a given complex.

33. Use of a molecule that modulates the amount of, activity of, or the protein components of the complex of any one of Claim 1 - 8 for the manufacture of a medicament for the treatment or prevention of a disease or disorder, preferentially of a disease or disorder such as those as stated in column 2, table 4 of a given complex.

34. A method for the production of a pharmaceutical composition comprising carrying out the method of Claim 26 - 31 to identify a molecule that modulates the function, activity, composition or formation of said complex, and further comprising mixing the identified molecule with a pharmaceutically acceptable carrier. 404

35. A method for diagnosing or screening for the presence of a disease or disorder or a predisposition for developing a disease or disorder in a subject, which disease or disorder is characterized by an aberrant amount of, component disposition of, or intracellular localization of the complex of any one of the Claim 1 - 8, comprising determining the amount of, activity of, protein components of, and/or intracellular localization of, said complex and/or the transcription level of a gene regulated by the complex and/or the abundance and/or activity of a protein or protein complex dependent on the function of the complex and/or product of a gene dependent on the complex in a comparative sample derived from a subject, wherein a difference in said amount, activity, or protein components of, said complex in a corresponding sample from a subject not having the disease or disorder or predisposition indicated the presence in the subject of the disease or disorder or predisposition in the subject.

36. The method of Claim 35, wherein the amount of said complex is determined.

37. The method of Claim 35, wherein the activity of said complex is determined.

38. The method of Claim 37, wherein said determining step comprises isolating from the cell or organism said complex to produce said isolated complex and contacting said isolated complex in the presence or absence of a candidate molecule with a substrate of said complex and determining whether said substrate is processed in the absence of the candidate molecule and whether the processing of said substrate is modified in the presence of said candidate molecule.

39. The method of Claim 35, wherein the amount of the individual protein components of said complex is determined.

40. The method of Claim 39, wherein said determining step comprises determining whether any of the proteins according to Claim 13 is present in the complex.

41. The complex of any one of Claim 1 - 8, or a protein of Claim 13 or an antibody or fragment thereof of Claim 17, for use in a method of diagnosing a disease or disorder, preferentially of a disease or disorder such as neurodegenerative disease such as those as stated in column 2, table 4 of a given complex. 405

42. A method for treating or preventing a disease or disorder characterized by an aberrant amount of, activity of, component composition of or intracellular localization of, the complex of any one of Claim 1 - 8, comprising administering to a subject in need of such treatment or prevention a therapeutically effective amount of one or more molecules that modulate the amount of, activity of, or protein composition of, said complex.

43. The method according to Claim 42, wherein said disease or disorder involves decreased levels of the amount or activity of said complex.

44. The method according to Claim 42, wherein said disease or disorder involves increased levels of the amount or activity of said complex.

45. Complex of Claim 1 - 8 and/or a protein as listed in table 1 , fifth column of said complex as a target for an active agent of a pharmaceutical, preferably a drug target, in the treatment or prevention of a disease or disorder, preferentially of a disease or disorder such as a neurodegenerative disease such as those as stated in column 2, table 4 of a given complex.