Chemistry: molecular biology and microbiology – Measuring or testing process involving enzymes or... – Involving nucleic acid
Patent
1995-06-07
1999-01-12
Ketter, James
Chemistry: molecular biology and microbiology
Measuring or testing process involving enzymes or...
Involving nucleic acid
435 696, 435 911, C12Q 168
Patent
active
058586571
ABSTRACT:
The invention provides methods and kits for producing specific binding pairs (sbp) members. Populations of polypeptide chain components of sbp members are combined to form libraries of sbps displayed by secreted replicable genetic display packages (rgdp). At least one of the polypeptide chains is expressed as a fusion with a component of an rgdp which thereby displays that polypeptide chain at the surface of rgdp. At least one population of polypeptide chains is expressed from nucleic acid which is capable of being packaged using a component of an rgdp, whereby the genetic material of rgdps produced encodes a polypeptide chain. The methods enable production of libraries of multimeric sbp members from a very large number of possible combinations. In one embodiment of the invention a method employs "chain shuffling" in the production of sbp members of desired specificity for a counterpart sbp member. Selection procedures are also described.
REFERENCES:
patent: 4190495 (1980-02-01), Curtiss, III
patent: 4816397 (1989-03-01), Bass et al.
patent: 4946778 (1990-08-01), Ladner et al.
patent: 5223409 (1993-06-01), Ladner
Bass et al., "Hormone Phage: An Enrichment Method for Variant Proteins With Altered Binding Properties," Proteins, 8(4):309-314 (1990).
de la Cruz et al., "Immunogenicity and Epitope Mapping of Foreign Sequences via Genetically Engineered Filamentous Phage," J. Biol. Chem., 263(9):4318-4322 (Mar. 25, 1988).
Huse et al., "Generation of Large Combinatorial Library of the Immunoglobulin Repertoire in Phage Lambda," Science, 246:1275-1281 (1989).
Kang et al., "Linkage of Recognition and Replication Functions by Assembly Combinatorial Antibody Fab Libraries Along Phage Surface," Proc. Nat'l. Acad. Sci., USA, 88(10):4363-4366 (May 15, 1991).
McCafferty et al., "Phage Antibodies: Filamentous Phage Displaying Antibody Variable Domains," Nature, 348:552-554 (1990).
Milstein, C., "The Croonian Lecture, 1989. Antibodies: A Paradigm for the Biology of Molecular Recognition," Proc. R. Soc. London, B. Biol. Sci., 239:1-16 (1990).
Parmley & Smith, "Antibody-selectable Filamentous fd Phage Vectors: Affinity Purifications of Target Genes," Gene, 73(2):305-318 (Dec. 20, 1988).
Short et al., "Lambda ZAP: A Bacteriophage Lamda Expression Vector with In Vivo Excision Properties," Nucleic Acids Research, 16(15):7583-7600 (Aug. 11, 1988).
Smith, "Filamentous Fusion Phage: Novel Expression Vectors that Display Cloned Antigens on the Virion Surface," Science, 228(4705):1315-1317 (Jun. 14, 1985).
Tsunetsugu-Yokota et al., "Expression of an Immunogenic Region of HIV by a Filamentous Bacteriophage Vector," Gene, 99(2):261-265 (Mar. 15, 1991).
Winter & Milstein, "Man-made Antibodies," Nature, 349(6307):293-299 (Jan. 24, 1991).
Abremski et al., "Studies on the Properties of PI Site-Specific Recombination: Evidence for Topologically Unlinked Products following Recombination," Cell, 32:1301-1311 (Apr., 1983).
Better et al., "Escherichia coli Secretion of an Active Chimeric Antibody Fragment," Science, 240:1041-1043 (1988).
Boyd, A.C., "Turbo Cloning: A Fast, Efficient Method for Cloning PCR Products and Other Blunt-ended DNA Fragments into Plasmids," Nucleic Acids Research, 21(4):817-821 (1993).
Clonetech, cDNA & Genomic Libraries, Clontech Laboratories, Inc., Palo Alto, California, USA, pp. 75-96 & 192 (1995/1996).
Cregg et al., "Short Communication: Use of Site-Specific Recombination to Regenerate Selectable Markers," Mol. Gen. Genet., 219:320-323 (1989).
Dale et al., "Gene Transfer with Subsequent Removal of the Selection Gene from the Host Genome," Proc. Nat'l Acad. Sci., USA, 88:10558-10562 (Dec., 1991).
Dower et al., "High Efficiency Transformation of E. coli by High Voltage Electroporation," Nucleic Acids Research, 16(13):6127-6145 (1988).
Fukushige et al., "Genomic Targeting with a Positive-selection lox Integration Vector Allows Highly Reproducible Gene Expression in Mammalian Cells," Proc. Nat'l Acad. Sci., 89:7905-7909.
Griffiths et al., "Isolation of High Affinity Human Antibodies Directly from Large Synthetic Repertoires," EMBO J., 13(14):3245-3260 (1994).
Hoess et al., "The Cre-lox Recombination System," Nucleic Acids and Molecular Biology, vol. 4, Eckstein et al., (Eds.), Springer-Verlag Berlin Heidelberg, pp. 99-109 (1990).
Hoess et al., "The Role of the loxP Spacer Region in P1 Site-specific Recombination," Nucleic Acids Research, 14(5):2287-2300 (1986).
Landy, A., "Mechanistic and Structural Complexity in the Site-specific Recombination Pathways of Int and FLP," Current Opinion in Genetics and Development, 3:699-707 (1993).
Lane et al., "Epitope Mapping Using Bacteriophage Peptide Libraries," Curr. Opin. Immunol., 5:268-271 (1993).
Neidhardt, F.C., (Ed.), Escherichia coli and Salmonella typhimurium, Cellular & Molecular Biology, American Society of Microbiology, Washington, D.C., pp. 1034-1043, 1054-1060, 1061-1070 (1987).
Orban et al., "Tissue- and Site-specific DNA Recombination in Transgenic Mice," Proc. Nat'l Acad. Sci., USA, 89:6861-6865 (Aug., 1992).
Palazzolo et al., "Phage Lambda cDNA Cloning Vectors for Subtractive Hybridization, Fusion-protein Synthesis and Cre-loxP Automatic Plasmid Subcloning," Gene, 88:25-36 (1990).
Parmley et al., "Filamentous Fusion Phage Cloning Vectors for the Study of Epitopes and Design of Vaccines," Adv. Exp. Med. Biol. 215-218 (1989).
Peakman et al., "Highly Efficient Generation of Recombinant Baculoviruses by Enzymatically Mediated Site-specific In Vitro Recombination," Nucleic Acids Research, 20(3):495-500 (1992).
Prave, P., (Ed.), Fundamentals of Biotechnology, VCH, Weinheim, Germany, pp. 307-308 (1987).
Qian et al., "Reactions between Half- and Full-FLP Recombination Target Sites," J. Biol. Chem., 267(11):7794-7805 (Apr. 15, 1992).
Sambrook et al., "Transformation of E. coli High-voltage Electroporation Electrotransformation," Molecular Cloning, A Laboratory Manual, Second Edition, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York, p. 1.75 (1989).
Siest et al., "Application of Gene Transfer Technologies to the Production of Enzyme Reference Materials: Example of Gamma-Glutamyltransferase," Clin. Chem., 39:1573-1589 (1993).
Skerra et al., "Assembly of a Functional Immunoglobulin F.sub.v Fragment in Escherichia coli," Science, 240:1038-1041 (1988).
Waterhouse et al., "Combinational Infection and In Vivo Recombination: A Strategy for Making large Phage Antibody Repertoires," Nucleic Acids Research, 21(9):2265-2266 (1993).
Griffiths Andrew David
Johnson Kevin Stuart
Smith Andrew John Hammond
Winter Gregory Paul
Cambridge Antibody Technology Limited
Ketter James
Medical Research Council
LandOfFree
Methods for producing members of specific binding pairs does not yet have a rating. At this time, there are no reviews or comments for this patent.
If you have personal experience with Methods for producing members of specific binding pairs, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Methods for producing members of specific binding pairs will most certainly appreciate the feedback.
Profile ID: LFUS-PAI-O-1514059