WO2005066631A1 - Use of fluiorinated nonionic surfactants for reducing nonspecific binding of molecules to a surface - Google Patents
Use of fluiorinated nonionic surfactants for reducing nonspecific binding of molecules to a surface Download PDFInfo
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- WO2005066631A1 WO2005066631A1 PCT/US2004/038054 US2004038054W WO2005066631A1 WO 2005066631 A1 WO2005066631 A1 WO 2005066631A1 US 2004038054 W US2004038054 W US 2004038054W WO 2005066631 A1 WO2005066631 A1 WO 2005066631A1
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
- G01N33/543—Immunoassay; Biospecific binding assay; Materials therefor with an insoluble carrier for immobilising immunochemicals
- G01N33/54393—Improving reaction conditions or stability, e.g. by coating or irradiation of surface, by reduction of non-specific binding, by promotion of specific binding
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6813—Hybridisation assays
- C12Q1/6832—Enhancement of hybridisation reaction
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S435/00—Chemistry: molecular biology and microbiology
- Y10S435/962—Prevention or removal of interfering materials or reactants or other treatment to enhance results, e.g. determining or preventing nonspecific binding
Definitions
- target molecules such as polypeptides
- affinity separation can be defined as any separation achieved by employing the specific binding of one molecule or a group of molecules by another molecule or a group of molecules.
- Affinity separation is used to capture an analyte (e.g., typically a macromolecule, such as a protein or nucleic acid) from a complex mixture such as serum or plasma. After capturing the analyte, the contaminants are washed away and the analyte (i.e., target molecule) is detected using well known assay protocols and/or removed from the solid phase material for further processing.
- Solid support materials i.e., solid phase materials
- affinity chromatography are well known and typically include the attachment of a ligand or binder to the carrier.
- Many solid support materials demonstrate nonspecific binding of unwanted components such as proteins that do not have specific interactions with the ligand.
- Attempts to improve on affinity supports have involved the use of an inert perfluorocarbon polymer carrier with ligands or binders attached to its surface through a liighly fluorinated isocyanate anchor group (see, e.g., U.S. Pat. No. 4,954,444 (Eveleigh et al.)).
- No. 4,619,897 discloses the immobilization of enzymes onto a fluorine resin membrane which is made hydrophilic on one side by the penetration of a perfluoroalkyl surface active agent to a prescribed depth.
- the asymmetrically functional membrane thus obtained is then treated with an enzyme and a crosslinking agent such as glutaraldehyde to achieve enzyme immobilization.
- affinity separation as well as other separations involving solid supports are such powerful techniques and because currently available supports suffer from various disadvantages, there is a need for improved methods and materials, which may or may not actually function as an affinity support.
- the discussion of prior publications and other prior knowledge does not constitute an admission that such material was published, known, or part of the common general knowledge.
- the present invention provides materials, methods, and kits for reducing nonspecific binding of molecules to a surface. More specifically, in certain embodiments, the present invention provides materials, methods, and kits for isolation of particular target molecules (e.g., polypeptides) from a sample, and more particularly for decreasing the loss of the target material due to nonspecific binding to a solid phase material. In one embodiment, the present invention provides a method of reducing nonspecific binding of target molecules to a surface.
- target molecules e.g., polypeptides
- the method includes: providing a sample that includes target molecules; providing a solid phase material that includes a hydrophobic portion and capture sites; providing a fluorinated nonionic surfactant that includes two or more fluorinated hydrophobic segments and one or more hydrophilic segments; optionally providing a secondary blocking agent; contacting the solid phase material with the fluorinated nonionic surfactant and optionally contacting the solid phase material with the secondary blocking agent to block at least a portion of the hydrophobic portion of the solid phase material (i.e., the surface involved in nonspecific binding); contacting the blocked solid phase material with the sample to adhere at least a portion of the target molecules of the sample to the capture sites; and optionally removing at least a portion of the adhered target molecules of the sample from the blocked solid phase material.
- the capture sites can include hydrophobically attached or covalently attached groups or molecules.
- the present invention provides a method of reducing nonspecific binding of target molecules to a surface.
- the method includes: providing a sample that includes target molecules; providing a solid phase material that includes a polytetrafluoroethylene fibril matrix and sorptive particles (i.e., particles that include the capture sites) enmeshed in the matrix; providing a fluorinated nonionic surfactant that includes two or more fluorinated hydrophobic segments and one or more hydrophilic segments; optionally providing a secondary blocking agent; contacting the solid phase material with the fluorinated nonionic surfactant and optionally contacting the solid phase material with the secondary blocking agent to block at least a portion of the polytetrafluoroethylene fibril matrix (i.e., the surface of the solid phase material involved in nonspecific binding); contacting the blocked solid phase material with the sample to adhere at least a portion of the target molecules of the biological sample to the sorptive particles; and
- the present invention provides a method of reducing nonspecific binding of molecules to a surface.
- the method includes: providing a solid phase material that includes a hydrophobic portion; providing a fluorinated nonionic surfactant that includes two or more fluorinated hydrophobic segments and one or more hydrophilic segments; optionally providing a secondary blocking agent; and contacting the solid phase material with the fluorinated nonionic surfactant and optionally contacting the solid phase material with the secondary blocking agent to block at least portion of the hydrophobic portion (i.e., the surface of the solid phase material involved in nonspecific binding).
- the present invention provides a method of reducing nonspecific binding of target molecules to a surface.
- the method includes: providing a sample that includes target molecules; providing a solid phase material that includes a hydrophobic portion and one or more hydrophobically attached capture proteins; providing a fluorinated nonionic surfactant that includes two or more fluorinated hydrophobic segments and one or more hydrophilic segments; contacting the solid phase material with the fluorinated nonionic surfactant to block at least a portion of the hydrophobic portion of the solid phase material; contacting the blocked solid phase material with the sample to adhere at least a portion of the target molecules of the sample to the one or more capture proteins; and optionally removing at least a portion of the adhered target molecules of the sample from the blocked solid phase material.
- a method of modifying a surface is provided.
- the method includes: providing a solid phase material that includes a hydrophobic portion; providing a protein and contacting the protein to the solid phase material to hydrophobically attach the protein; providing a fluorinated nonionic surfactant that includes two or more fluorinated hydrophobic segments and one or more hydrophilic segments; and contacting the solid phase material with the fluorinated nonionic surfactant to reduce nonspecific binding of other molecules to the solid phase material.
- the present invention also provides kits for carrying out the various methods of the present invention.
- a kit in one embodiment, includes: a solid phase material that includes a hydrophobic portion; a fluorinated nonionic surfactant that includes two or more fluorinated hydrophobic segments and one or more hydrophilic segments; an optional secondary blocking agent; and instructions for carrying out a method of the present invention. If desired, in the kit the fluorinated nonionic surfactant is disposed on the solid phase material.
- a kit in another embodiment, includes: a solid phase material that includes a polytetrafluoroethylene fibril matrix and sorptive particles enmeshed in the matrix; a fluorinated nonionic surfactant that includes two or more fluorinated hydrophobic segments and one or more hydrophilic segments; an optional secondary blocking agent; and instructions for carrying out a method of the present invention.
- the present invention also provides solid phase materials.
- the present invention provides a material that includes a solid phase material having a fluorinated nonionic surfactant disposed thereon; wherein: the solid phase material includes a polytetrafluoroethylene fibril matrix and sorptive particles enmeshed in the matrix; and the fluorinated nonionic surfactant includes two or more fluorinated hydrophobic segments and one or more hydrophilic segments.
- the present invention provides a material that includes a solid phase material having a fluorinated nonionic surfactant disposed thereon; wherein: the solid phase material includes a thermally induced phase separation membrane; and the fluorinated nonionic surfactant includes two or more fluorinated hydrophobic segments and one or more hydrophilic segments.
- the present invention provides a material that includes a solid phase material having a fluorinated nonionic surfactant disposed thereon; wherein: the solid phase material includes a high internal phase emulsion foam; and the fluorinated nonionic surfactant includes two or more fluorinated hydrophobic segments and one or more hydrophilic segments.
- Polypeptide refers to a polymer of amino acids and does not refer to a specific length of a polymer of amino acids.
- peptide, oligopeptide, protein, and enzyme are included within the definition of polypeptide, whether naturally occurring or synthetically derived, for instance, by recombinant techniques or chemically or enzymatically synthesized. This term also includes post- expression modifications of the polypeptide, for example, glycosylations, acetylations, phosphorylations, and the like.
- Polynucleotide and “nucleic acid” are used interchangeably to refer to a polymeric form of nucleotides of any length, and further refer to DNA (e.g., genomic DNA, cDNA, or plasmid DNA), RNA (e.g., mRNA, tRNA, or rRNA), and PNA. It can be in a wide variety of forms, including, without limitation, double-stranded or single- stranded configurations, circular form, plasmids, relatively short oligonucleotides, peptide nucleic acids also called PNA's (as described in Nielsen et al., Chem. Soc. Rev., 26, 73-78 (1997)), and the like.
- the nucleic acid can be genomic DNA, which can include an entire chromosome or a portion of a chromosome.
- the DNA can include coding (e.g., for coding mRNA, tRNA, and/or rRNA) and/or noncoding sequences (e.g., centromeres, telomeres, intergenic regions, introns, transposons, and/or microsatelhte sequences).
- the nucleic acid can include any of the naturally occurring nucleotides as well as artificial or chemically modified nucleotides, mutated nucleotides, etc.
- the nucleic acid can include a non-nucleic acid component, e.g., peptides (as in PNA's), labels (radioactive isotopes or fluorescent markers), and the like.
- a non-nucleic acid component e.g., peptides (as in PNA's), labels (radioactive isotopes or fluorescent markers), and the like.
- isolated refers to target molecules (i.e., target material) that have been removed from the sample in which they are originally found. This includes simply concentrating the target molecules without necessarily removing any other materials other than the original solvent in the original sample. It also includes separating the target molecules from other materials, e.g., cellular components such as lipids, salts, etc. More preferably, the isolated target molecules are substantially purified.
- substantially purified refers to target material that is at least 50%, preferably at least 80%, and more preferably at least 95%, pure with respect to removal of a contaminant, e.g., cellular components such as lipids or salts. These percentages refer to the amount of target molecules (e.g., proteins, DNA, RNA, PNA) relative to the total amount of the target molecules and contaminants other than the solvent in the sample.
- target molecules e.g., proteins, DNA, RNA, PNA
- substantially purified generally refers to separation of a majority of cellular components or reaction contaminants from the sample, so that compounds capable of interfering with the subsequent use of the isolated target molecules are removed.
- “Adheres to” or “adherance” or “binding” refer to reversible retention via a wide variety of mechanisms, including weak forces such as Van der Waals interactions, electrostatic interactions, affinity binding, or physical trapping. The use of this term does not imply a mechanism of action, and includes adsorptive and absorptive mechanisms.
- “Capture sites” refer to sites on the solid phase material to which a material adheres. Typically, the capture sites include functional groups or molecules that are either covalently attached or hydrophobically attached to the solid phase material.
- “Nonspecific binding” refers to adherence of molecules to a surface of a solid phase material through a hydrophobic interaction in a manner not specified by that material's construction.
- Solid phase material refers to a material that may include a wide variety of organic and/or inorganic materials. Such materials may be made of a polymer made of repeating units, which may be the same or different, of organic and/or inorganic compounds of natural and/or synthetic origin.
- “Surfactant” refers to a substance that lowers the surface or interfacial tension of the medium in which it is dissolved.
- the terms “comprises” and variations thereof do not have a limiting meaning where these terms appear in the description and claims. As used herein, “a,” “an,” “the,” “at least one,” and “one or more” are used interchangeably and mean one or more.
- the present invention provides methods and kits for reducing nonspecific binding of molecules to a surface. More specifically, the methods and kits of the present invention are useful for reducing the loss of the target material due to nonspecific binding to a solid phase material. Even more specifically, the present invention provides methods for the isolation, and preferably purification and recovery, of target molecules, such as polypeptides and polynucleotides (i.e., nucleic acid), as well as small organic molecules, from a sample. Alternatively, certain methods and kits of the present invention are useful for reducing undesirable binding of molecules, which is useful in ELISA's and other immunoassays, protein blotting assays, and protein-protein interaction assays.
- the solid phase material includes a hydrophobic portion and capture sites. These capture sites can be attached in a variety of ways to the solid phase material. For example, they can be covalently attached or they can be hydrophobically attached to the solid phase material. For example, if the solid phase material includes sorptive particles, these particles typically include the capture sites, which are typically provided by ligands capable of binding to (i.e., capturing) target molecules. Alternatively, if the solid phase material has no such sorptive particles hydrophobic capture molecules can be attached to the hydrophobic portion of the solid phase material through hydrophobic interactions, for example. Such hydrophobically attached molecules are typically proteins that are capable of binding to (i.e., capturing) target molecules.
- the nonspecific binding of molecules e.g., as in a target material
- a solid phase material which includes a hydrophobic portion
- the fluorinated nonionic surfactant includes two or more fluorinated hydrophobic segments and one or more hydrophilic segments.
- the solid phase material can also be contacted with a secondary blocking agent (e.g., a blocking protein) for further reduction in nonspecific binding.
- the reduction (i.e., decrease) in nonspecific binding of molecules to a surface is relative to the surface without being pretreated with the fluorinated nonionic surfactant.
- the capture sites are provided by capture molecules (e.g., capture proteins) hydrophobically attached to the solid phase material, it has been surprisingly discovered that the surfactant described herein does not remove such capture sites.
- Materials isolated according to the invention will be useful, for example, in assays for detection of the presence of a particular target molecule (e.g., nucleic acid or protein) in a sample. Such assays are important in the prediction and diagnosis of disease, forensic medicine, epidemiology, and public health.
- isolated DNA may be subjected to hybridization and/or amplification to detect the presence of an infectious virus or a mutant gene in an individual, allowing determination of the probability that the individual will suffer from a disease of infectious or genetic origin, hi another example, isolated antibodies or antigens can be used to diagnose disease.
- the ability to detect an infectious virus or a mutation in one sample among the hundreds or thousands of samples being screened takes on substantial importance in the early diagnosis or epidemiology of an at- risk population for disease, e.g., the early detection of HIV infection, cancer or susceptibility to cancer, or in the screening of newborns for diseases, where early detection may be instrumental in diagnosis and treatment, hi addition, the method can also be used in basic research laboratories to isolate nucleic acid or proteins from cultured cells or biochemical reactions.
- a sample containing target material i.e., target molecules
- a flow-through receptacle although this receptacle is not a necessary requirement of the present invention.
- the solid phase material useful in the methods of the present invention may include a wide variety of organic and/or inorganic materials. Preferred materials are capable of retaining target molecules (e.g., biomolecules such as proteins). Such materials include a hydrophobic portion, which in the context of the present invention means a material that has a critical surface tension of less than the surface tension of water (e.g., less than 72 dynes/cm), and preferably less than the critical surface tension of nylon (e.g., less than 43 dynes/cm).
- the solid phase material includes an organic polymeric matrix. The solid phase material is preferably dried to a generally stable moisture content. It is typically then stored dry to maintain that stable moisture content.
- suitable materials are chemically inert, physically and chemically stable, and compatible with a variety of biological samples.
- suitable polymers include, for example, polyolefms and fluorinated polymers.
- the solid phase material is typically washed to remove salts and other contaminants prior to use.
- the solid phase material is preferably used in a flow-through receptacle, for example, such as a pipet, syringe, or larger column, microtiter plate, or microfluidic device, although suspension methods that do not involve such receptacles could also be used.
- the solid phase material useful in the methods of the present invention can include a wide variety of materials in a wide variety of forms.
- the solid phase material can be in the form of particles or beads, which may be loose or immobilized, fibers, foams, frits, microporous films, membranes, or a substrate with microreplicated surface(s).
- the solid phase material includes particles, they are preferably uniform, spherical, and rigid to ensure good fluid flow characteristics.
- such materials are typically in the form of a loose, porous network to allow uniform and unimpaired entry and exit of large molecules and to provide a large surface area.
- the solid phase material has a relatively high surface area, such as, for example, more than one meter squared per gram (m 2 /g).
- the solid phase material may or may not be in a porous matrix.
- membranes can also be useful in certain methods of the present invention.
- particles or beads they may be introduced to the sample or the sample introduced into a bed of particles/beads and removed therefrom by centrifuging, for example.
- particles/beads can be coated (e.g., pattern coated) onto an inert substrate (e.g., polycarbonate or polyethylene), optionally coated with an adhesive, by a variety of methods (e.g., spray drying).
- the substrate can be microreplicated for increased surface area and enhanced clean-up.
- the solid phase material includes a fibril matrix, which may or may not have particles enmeshed therein.
- the fibril matrix can include any of a wide variety of fibers. Typically, the fibers are insoluble in an aqueous environment.
- the fibril matrix forms a web that is at least 15 microns, and no greater than 1 millimeter, and more preferably, no greater than 500 microns thick.
- the particles are typically insoluble in an aqueous environment. They can be made of one material or a combination of materials, such as in a coated particle. They can be swellable or nonswellable.
- the coating is preferably an aqueous- or organic- insoluble material.
- the coating may or may not be one to which target molecules, such as proteins, will adhere.
- the base particle that is coated can be inorganic or organic.
- the base particles can include inorganic oxides such as silica, alumina, titania, zirconia, etc., to which are covalently bonded organic groups. Examples of suitable solid phase materials that include a fibril matrix are described in U.S. Pat. Nos.
- RE 36,811 discloses a solid phase extraction medium that includes: a PTFE fibril matrix, and sorptive particles enmeshed in the matrix, wherein the particles include more than 30 and up to 100 weight percent of porous organic particles, and less than 70 to 0 weight percent of porous (organic-coated or uncoated) inorganic particles, the ratio of sorptive particles to PTFE being in the range of 40:1 to 1:4 by weight.
- Particularly preferred solid phase materials are available under the trade designation EMPORE from the 3M Company, St. Paul, MN.
- the fundamental basis of the EMPORE technology is the ability to create a particle-loaded membrane, or disk, using any sorbent particle.
- the particles are tightly held together within an inert matrix of polytetrafluoroethylene (typically 90% sorbent: 10% PTFE, by weight).
- the PTFE fibrils do not substantially interfere with the activity of the particles.
- the EMPORE membrane fabrication process results in a denser, more uniform extraction medium than can be achieved in a traditional Solid Phase Extraction (SPE) column or cartridge prepared with the same size particles.
- the solid phase material e.g., a microporous thermoplastic polymeric support
- Particles are spaced from one another to provide a network of micropores therebetween. Particles are connected to each other by fibrils, which radiate from each particle to the adjacent particles. Either, or both, the particles or fibrils may be hydrophobic. Examples of such preferred materials have a high surface area, often as high as 40 meters /gram as measured by Hg surface area techniques and pore sizes up to 5 microns. This type of fibrous material can be made by a preferred technique that involves the use of induced phase separation.
- thermoplastic polymer This involves melt blending a thermoplastic polymer with an immiscible liquid at a temperature sufficient to form a homogeneous mixture, forming an article from the solution into the desired shape, cooling the shaped article so as to induce phase separation of the liquid and the polymer, and to ultimately solidify the polymer and remove a substantial portion of the liquid leaving a microporous polymer matrix.
- This method and the preferred materials are described in detail in U.S. Pat. Nos. 4,726,989 (Mrozinski), 4,957,943 (McAllister et al), and 4,539,256 (Shipman). Such materials are referred to as thermally induced phase separation membranes (TIPS membranes) and are particularly preferred.
- suitable solid phase materials include nonwoven materials as disclosed in U.S. Pat. No. 5,328,758 (Markell et al.). This material includes a compressed or fused particulate-containing nonwoven web (preferably blown microfibrous) that includes high sorptive-efficiency chromatographic grade particles.
- suitable solid phase materials include those known as HIPE Foams, which are described, for example, in U.S. Pat. Pub. No. 2003/0011092 (Tan et al.).
- HIPE high internal phase emulsion
- a continuous reactive phase typically an oil phase
- a discontinuous or co-continuous phase immiscible with the oil phase typically a water phase
- the immiscible phase includes at least 74 volume percent of the emulsion.
- Many polymeric foams made from HEPE's are typically relatively open-celled. This means that most or all of the cells are in unobstructed communication with adjoining cells. The cells in such substantially open-celled foam structures have intercellular windows that are typically large enough to permit fluid transfer from one cell to another within the foam structure.
- the solid phase material includes functional groups that bind target molecules.
- the solid phase material will have reactive functional groups or be treated to have reactive functional groups that are capable of forming covalent bonds with ligand molecules or groups of ligand molecules.
- These covalently bonded ligand molecules which form the capture sites in certain embodiments of the invention, will bind target molecules from samples.
- U.S. Pat. No. 5,999,935 discloses a solid phase material that includes: covalently reactive particles incorporated within a continuous, porous matrix, said reactive particles having surfaces that includes covalently reactive functional groups capable of directly forming covalent chemical bonds with nucleophilic ligands without need for an intermediate activation step.
- examples of solid phase materials may be solid phase materials containing any one of several commercially available beads with reactive chemistries such as EMPHAZE (3M Company, Saint Paul, MN).
- Ligands such as polypeptides, nucleic acids, small molecules may be coupled covalently to these solid phase materials using procedures supplied by the manufacturers of the beads.
- the capture sites can also be provided by hydrophobically attached molecules. These include, for example, proteins such as those used in affinity chemistries. These include, but are not limited to, Protein A, Protein G, avidin, streptavidin, lectins such as jacaline and concanavolin A, antibodies, and receptor proteins.
- capture sites include, but are not limited to, metal affinity ligands, boronates, protein binding dyes such as Cibacron Blue 3GA, polypeptides, Protein A mimetics, and oligonucleotides.
- Such capture molecules can be added to the solid phase material in a variety of ways. Typically, they are added by saturating the solid phase material with an aqueous solution of the capture molecules, which may include a variety of salt concentrations. Various combinations or mixtures of capture sites can be incorporated into a solid phase material.
- the nonspecific binding of molecules to a solid phase material is decreased by treatment with a nonionic fluorinated surfactant.
- the fluorinated surfactant includes two or more fluorinated hydrophobic segments and one or more hydrophilic segments.
- a hydrophobic segment is defined as one that preferentially orients itself within the organic phase at the water-organic interface of a dispersion of the surfactant in a water-organic two-phase mixture.
- a hydrophilic segment is defined as one that orients itself within the water phase in the above system.
- the surfactant can be applied using an aqueous solution of the surfactant, although organic solvents can be used if desired.
- the surfactant can be applied neat or as a solution or dispersion, which can be in a wide range of concentrations.
- the surfactant can be applied using coating techniques such as dipping, flow-through coating, knife coating, etc. After application of the surfactant, the surface is typically washed to remove excess surfactant, but surprisingly this still provides beneficial results. Although it is not necessarily a limitation of the invention, it is believed that this results in the surfactant forming a monolayer on the solid phase material.
- the surfactant can be applied to a solid phase material and dried, thereby forming a thicker layer.
- fluorinated surfactants include those available under the trade designation ZONYL from DuPont (Wilmington, DE), such as ZONYL FSN, FSN-100, FSO-100, and FSO-300, which are fluoro-polyoxyethylene surfactants, and NOVEC FC4432 and FC4430 from 3M Company (St. Paul, MN).
- the fluorosurfactants appear to coat the surface of the solid phase material thereby preventing binding of other materials.
- fluorinated surfactants are derived from nonafluorobutanesulfonyl fluoride that contains polyalkyleneoxy side chains and may be copolymerized with acrylic acid or methacrylic acid to form polyacrylates or polymethacrylates. Specific examples are disclosed, for example, in U.S. Pat. Publication Nos. 2003/0139550 (Savu et al.) and 2003/0139549 (Savu et al.).
- fluorinated surfactants include at least one unit of the following formula (I):
- fluorinated surfactants are of the following formula (IT):
- the rectangular box represents a bond in a polymerizable or polymer chain
- R, R , and R are each independently hydrogen or a C1-C4 alkyl group (preferably, hydrogen or methyl)
- R 3 is a straight or branched alkylene-oxy group, linked together and having 2-6 carbon atoms, or a straight or branched alkylene group having 12-20 carbon atoms
- x, y, and z are each independently at least 1.
- R 3 of the surfactant of Formula II is a group of the formula (EO)p-(PO) q -(EO)p or (PO) q -(EO) p -(PO) q .
- p is an integer of 1 to 128 and q is an integer of 0 to 54.
- R of the surfactant of Formula II is of the formula (PO) q - (EO) p -(PO) q .
- R and R 1 are methyl, q is 0, and p is 4 to 10. hi certain embodiments, q is 9 to 22 and p is 14 to 164.
- R of the surfactant of Formula II is of the formula (EO) p - (PO) q -(EO) p .
- p is an integer of 7 to 128 and q is an integer of 21 to 54.
- p is 11 and q is 21.
- the methods of the present invention can be used to isolate target molecules (e.g., biological macromolecules, such as polypeptides and polynucleotides, and small organic molecules) from a wide variety of samples, particularly biological samples, such as body fluids (e.g., whole blood, blood serum, urine, saliva, cerebral spinal fluid, semen, or synovial lymphatic fluid), various tissues (e.g., skin, hair, fur, feces, tumors, or organs such as liver or spleen), cell cultures or cell culture supematants, etc.
- the sample can be a food sample, a beverage sample, a fermentation broth, a clinical sample used to diagnose, treat, monitor, or cure a disease or disorder, a forensic sample, or an agricultural sample
- Bio samples are those of biological or biochemical origin. Those suitable for use in the methods of the present invention can be derived from mammalian, plant, bacterial, or yeast sources.
- the biological sample can be in the form of single cells, in the form of a tissue, or fluids of biologic origin. Cells or tissue can be derived from in vitro culture.
- certain embodiments of the invention use whole blood without any preprocessing (e.g., lysing, filtering, etc.). Alternatively, whole blood can be preprocessed and the fractions used as the sample in the methods of the invention.
- the sample can be a solid sample (e.g., solid tissue) that is dissolved or dispersed in water or an organic medium.
- the sample can be an organ homogenate (e.g., liver, spleen).
- the type of sample is not a limitation of the present invention.
- the isolated target molecules e.g., polypeptides, DNA, or RNA
- polypeptides can be used, preferably without further purification or washing, for a wide variety of applications.
- polypeptides can be used in the quantification of target molecules in samples, qualitative identification of immuno-complexes formed with the ligand molecules, testing activity of coupled ligand, and the like.
- nucleic acids can be used for amplification, sequencing, labeling, annealing, restriction digest, ligation, reverse transcriptase, hybridization, Southern blot, Northern blot, and the like.
- the target molecules may be isolated according to the invention from an impure, partially pure, or a pure sample. The purity of the original sample is not critical, as target molecules may be isolated from even grossly impure samples. If an original sample of higher purity is desired, the sample may be treated according to any conventional means known to those of skill in the art prior to undergoing the methods of the present invention. For example, the sample may be processed so as to remove certain impurities such as insoluble materials prior to subjecting the sample to a method of the present invention.
- the target molecules may be polypeptides, polynucleotides (i.e., nucleic acid), or small organic molecules.
- the target molecules may be of any molecular weight.
- polypeptides maybe from a few amino acids long to thousands of amino acids long, large and small intact proteins with post-expression modifications, modified polypeptides with any number and size of chemical modifications and functional groups.
- the sample containing the target molecules may be in a wide variety of volumes.
- the applied volume maybe as large as 1 liter or as small as 1 ⁇ L, or even less.
- the sample size typically varies depending on the desired application and equipment.
- the amount of target material that can be removed from the solid phase material according to the methods of the present invention is more than can be removed when a fluorinated nonionic surfactant is not used.
- the amount of target material that can be removed from the solid phase material treated with a fluorinated nonionic surfactant is preferably in an amount of at least 50%, more preferably at least 70%, even more preferably at least 90%, and even more preferably at least 98%, of the adhered target molecules.
- elution buffers examples include glycine-acetic acid, trifluoroacetic acid, N-[2-Hydroxyethyl]piperazine-N'-[2-ethanesulfonic acid] (HEPES), 3-[N- Morpholino]propanesulfonic acid (MOPS), piperazine-N,N'-bis[2-ethanesulfonic acid] (PIPES), 2-[N-Morpholino]ethansulfonic acid (MES), TRIS-EDTA (TE) buffer, sodium citrate, ammonium acetate, carbonate salts, and bicarbonates, etc. Various combinations of such materials can be used.
- the concentration of an elution buffer in an eluting reagent can be readily determined by one of skill in the art.
- the amount of eluting reagent used depends on several factors including desired recovery of captured target, format of device in which method is carried out, maximum tolerable dilution of target, etc.
- the recovery of the captured target increases with increasing amounts of elution reagent and then tapers off for further elutions.
- Device formats (such as microfluidic devices) may limit the amount of elution reagent used due to space limitations. Using excess elution reagent will result in dilution of the target.
- the method of the invention can be conducted in filtration devices which facilitate the movement of solutions through solid phase materials (referred to as flow-through devices) by means including centrifugation, suction, or pressure.
- Other devices include microtiter plates and microfluidic devices.
- the methods can be used in a variety of devices, a variety of illustrative embodiments of microtiter devices are described in U.S. Pat. Nos. 5,264,184 (Aysta et al.), 5,464,541 (Aysta et al.), and 5,620,663 (Aysta et al.), and in U.S. Pat. Publication Nos.
- kits which can include a solid phase material either with or without a holder (for example, a filter holder such as a syringe filter holder or a spin filter holder, or a column with retaining frits at each end for retaining particulate material), a nonionic fluorinated surfactant (either neat or in a solution), optionally a secondary binding agent, and instructions for use (e.g., for adhering target molecules and optionally eluting such molecules).
- a holder for example, a filter holder such as a syringe filter holder or a spin filter holder, or a column with retaining frits at each end for retaining particulate material
- a nonionic fluorinated surfactant either neat or in a solution
- optionally a secondary binding agent optionally a secondary binding agent
- instructions for use e.g., for adhering target molecules and optionally eluting such molecules.
- kits that include a flow-through receptacle having a solid phase material therein and a nonionic fluorinated surfactant.
- Other components that could be included within kits of the present invention include conventional reagents such as wash solutions, coupling buffers, quenching buffers, blocking buffers, elution buffers, and the like.
- Other components that could be included within kits of the present invention include conventional equipment such as spin columns, cartridges, 96-well filter plates, syringe filters, collection units, syringes, and the like.
- the kits typically include packaging material, which refers to one or more physical structures used to house the contents of the kit.
- the packaging material can be constructed by well-known methods, preferably to provide a contaminant-free environment.
- the packaging material may have a label that indicates the contents of the kit. hi addition, the kit contains printed instructions indicating how the materials within the kit are employed.
- the term "package” refers to a solid matrix or material such as glass, plastic, paper, foil, and the like.
- Instructions typically include a tangible expression describing the various methods of the present invention, including, for example, preparation of the solid phase material, the relative amounts of reagents and samples, maintenance time periods, temperature, buffer conditions, and the like.
- Target molecules may be separated from samples using a technique known as affinity purification, hi this technique, ligand molecules that interact specifically with the target molecules are identified. These ligand molecules are attached or immobilized (either covalently or non-covalently) to solid phase material which form the affinity purification supports. Such supports maybe exposed to blocking agents to block open adsorption sites. Samples are allowed to interact with the ligand molecules on the solid phase materials wherein some of the target molecules in the sample bind to the ligands. These bound target molecules are retained on the solid phase material when the sample is removed. Further washing may be performed to remove non-target molecules from the solid phase material. Finally some of the bound target molecules are eluted using elution reagents.
- These purified target molecules are said to be purified by affinity purification.
- Groups of target molecules that interact together in specific situations may be identified and purified from samples using a technique known as immuno-complex separation or protein-to-protein interaction separations.
- immuno-complex separation or protein-to-protein interaction separations In this technique, one or multiple ligand molecules that form part of the complex with the target molecules are identified.
- These ligand molecules are attached or immobilized (either covalently or non-covalently) to solid phase material which form the affinity purification supports. Such supports may be exposed to blocking agents to block open adsorption sites. Samples are allowed to interact with the ligand molecules on the solid phase materials wherein some of the target molecules in the sample bind to the ligands and form complexes.
- bound target molecule complexes are retained on the solid phase material when the sample is removed. Further gentle washing may be performed to remove molecules that are not part of these complexes, from the solid phase material. Finally some of the bound target molecule complexes are eluted using elution reagents, hnmuno-complex capture or protein-to-protein complex capture can be used in studying the function and association of proteins in biologic systems. The same principles can also be used to study the function and association of other molecules. Certain embodiments of the present invention, particularly those in which the capture sites are provided by molecules that hydrophobically attach to the solid phase material, such as capture proteins, can be used in protein-based assays such as ELIS A' s and RIA's.
- PTFE PTFE membrane
- Protein A was prepared and derivatized with Protein A. This was blocked with a bovine serum albumin solution containing either a polymeric fluorocarbon nonionic surfactant or a nonfluorinated monomeric surfactant. The membrane was then challenged with a solution of radiolabled human IgG antibody under binding conditions. The membrane was then eluted and the eluate counted to determine the recovery of the IgG.
- test cartridges were prepared by securing 1.26 cm diameter disks of the membrane in the bottom of 6 mL polypropylene syringe barrels using friction fit polypropylene retainer rings.
- I- 125 labeled IgG Human IgG protein antibody (No. 009-0102, Rockland Co., Gilbertsville, PA) was labeled with radioactive iodine (1-125) using the method of Fraker and Speck (Bipchem Biophvs. Res. Commun., 80, 849-857 (1978)).
- Table 1 shows that using the nonionic polymeric fluorocarbon surfactant (NOVEC FC4432) resulted in a significantly higher recovery of the IgG.
- Membrane A membrane fabricated as described in Experiment 1 was used except it was formed into 0.77 cm disks and secured in the bottom of the wells of a 96 well polypropylene flow through plate (as disclosed in U.S. Pat. Nos. 5,264,184 (Aysta et al.), 5,464,541 (Aysta et al.), and 5,620,663 (Aysta et al.)) by polypropylene retainer rings. Solutions were drawn through the membrane by centrifugal force using a plate centrifuge.
- a 0.166-mL aliquot of binding buffer containing 500 micrograms of Protein A was pipetted into the wells of the plate and incubated for 30 minutes. This solution was then centrifuged out and into a collection plate. 2. The wells were then washed with 0.8 mL of washing buffer. 3. A 0.7-mL aliquot of quenching buffer was pipetted into each well and centrifuged out. A second 0.7-mL aliquot was added to each well and the plate incubated for two hours. This solution was centrifuged out and the wells washed with four aliquots of 0.8 mL of washing buffer. 4. A 0.7-mL aliquot of the blocking buffer or the washing buffer was added to each well and then centrifuged out.
- Example 3 Comparison of Blocking Using a Nonionic Polymeric Fluorosurfactant and a
- a polypropylene particle loaded fibrillated PTFE membrane was fabricated as described in using polypropylene powder (No. 140S, Micropowders, h e, Tarrytown, NY).
- the membrane contained about 90% by weight polypropylene and was approximately 0.8 mm thick. For this experiment, it was cut into 0.77-cm diameter disks and secured by polypropylene retainer rings to the bottom of empty 2.1 -cm polypropylene chromatography columns. Vacuum was used to draw solutions through the membrane.
- washing buffer Phosphate Buffered Saline (No. 28372, Pierce Inc., Rockford, IL) Fluorescein labeled IgG: IgG-FITC (No. F9636, Sigma Co., St. Louis, MO) 100 micrograms/mL in washing buffer
- Nonionic polymeric fluorosurfactant 0.1% NOVEC FC4430 fluorosurfactant in washing buffer
- Nonionic monomeric fluorosurfactant 0.1% ZONYL FSG fluorosurfactant (E.I. duPont deNemours & Co., Willmington, DL) in washing buffer
- Example 4 Use of Nonionic Polymeric Fluorocarbon Surfactant as a Blocking Agent for Affinity Solid Phase Extraction.
- This experiment illustrates that a nonionic polymeric fluorocarbon surfactant can be used as a blocking agent in an affinity extraction in which the affinity ligand is bound to a solid support by hydrophobic interaction only.
- Reagents The polypropylene membrane in 2.1 -cm chromatography columns, fluorescein labeled IgG solution (IgG-FITC), nonionic polymeric fluorocarbon surfactant solution (FC4430) and washing buffer (WB) were the same as used in Example 3.
- Protein A (rPA50, Repligen Corp., Waltham, MA) solution was prepared at 3 mg/mL in a 35 mM CHES buffer at pH 9.0 containing 1M sodium sulfate.
- the elution buffer (EB) was the same as used in Example 1.
- Membranes 1 and 2 were not treated with the Protein A solution. They were treated with 0.3 mL of the CHES/sulfate buffer in which the Protein A was dissolved. Membranes 3 and 4 were then treated with 0.3 mL of the Protein A solution. The membranes were then treated with the solutions summarized in Table 3. Aliquots (0.75 mL) of each solution were used except that 0.2 mL aliquots were used for the fluorescein labeled IgG (IgG-
- Membrane 1 was not treated with Protein A or the FC4430. It showed a marked fluorescence indicating that the IgG-FITC was bound and could not be removed with the elution buffer.
- Membrane 2 was not treated with Protein A but was treated with the FC4430. It showed no fluorescence indicating that no IgG-FITC was bound.
- Membrane 3 was treated with both the Protein A and the FC4430 but was not eluted. It showed a marked fluorescence indicating that the IgG-FITC was bound.
- Membrane 4 was treated with both Protein A and FC4430 and was eluted with the elution buffer. It showed no fluorescence indicating that no IgG was bound.
Abstract
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AU2004312739A AU2004312739A1 (en) | 2003-12-24 | 2004-11-15 | Use of fluorinated nonionic surfactants for reducing nonspecific binding of molecules to a surface |
CA002550820A CA2550820A1 (en) | 2003-12-24 | 2004-11-15 | Use of fluorinated nonionic surfactants for reducing nonspecific binding of molecules to a surface |
EP04810989A EP1706740A1 (en) | 2003-12-24 | 2004-11-15 | Use of fluorinated nonionic surfactants for reducing nonspecific binding of molecules to a surface |
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US10/810,738 US7727710B2 (en) | 2003-12-24 | 2004-03-26 | Materials, methods, and kits for reducing nonspecific binding of molecules to a surface |
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Also Published As
Publication number | Publication date |
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JP2007517217A (en) | 2007-06-28 |
CA2550820A1 (en) | 2005-07-21 |
EP1706740A1 (en) | 2006-10-04 |
US20050142563A1 (en) | 2005-06-30 |
US7727710B2 (en) | 2010-06-01 |
AU2004312739A1 (en) | 2005-07-21 |
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