METHODS FOR PRODUCING MEMBERS OF SPECIFIC BINDING PAIRS
A member of a specific binding pair (sbp) is identified by expressing DNA encoding a genetically diverse population of such sbp members in recombinant host cells in which the sbp members are displayed in functional form at the surface of a secreted recombinant genetic display package (rgdp) containi...
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creator | JOHNSON, KEVIN STUART POPE, ANTHONY RICHARD CLACKSON, TIMOTHY PIERS GRIFFITHS, ANDREW DAVID MCCAFFERTY, JOHN HOOGENBOOM, HENDRICUS RENERUS JACOBUS MATTHEUS JACKSON, RONALD HENRY CHISWELL, DAVID JOHN WINTER, GREGORY PAUL BONNERT, TIMOTHY PETER HOLLIGER, KASPAR PHILIPP MARKS, JAMES DAVID |
description | A member of a specific binding pair (sbp) is identified by expressing DNA encoding a genetically diverse population of such sbp members in recombinant host cells in which the sbp members are displayed in functional form at the surface of a secreted recombinant genetic display package (rgdp) containing DNA encoding the sbp member or a polypeptide component thereof, by virtue of the sbp member or a polypeptide component thereof being expressed as a fusion with a capsid component of the rgdp. The displayed sbps may be selected by affinity with a complementary sbp member, and the DNA recovered from selected rgdps for expression of the selected sbp members. Antibody sbp members may be thus obtained, with the different chains thereof expressed, one fused to the capsid component and the other in free form for association with the fusion partner polypeptide. A phagemid may be used as an expression vector, with said capsid fusion helping to package the phagemid DNA. Using this method libraries of DNA encoding respective chains of such multimeric sbp members may be combined, thereby obtaining a much greater genetic diversity in the sbp members than could easily be obtained by conventional methods. |
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The displayed sbps may be selected by affinity with a complementary sbp member, and the DNA recovered from selected rgdps for expression of the selected sbp members. Antibody sbp members may be thus obtained, with the different chains thereof expressed, one fused to the capsid component and the other in free form for association with the fusion partner polypeptide. A phagemid may be used as an expression vector, with said capsid fusion helping to package the phagemid DNA. Using this method libraries of DNA encoding respective chains of such multimeric sbp members may be combined, thereby obtaining a much greater genetic diversity in the sbp members than could easily be obtained by conventional methods.</description><language>eng</language><subject>BEER ; BIOCHEMISTRY ; CHEMISTRY ; COMBINATORIAL CHEMISTRY ; COMPOSITIONS THEREOF ; CULTURE MEDIA ; DERIVATIVES THEREOF ; ENZYMOLOGY ; FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIREDCHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERSFROM A RACEMIC MIXTURE ; INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIRCHEMICAL OR PHYSICAL PROPERTIES ; LIBRARIES, e.g. CHEMICAL LIBRARIES, IN SILICOLIBRARIES ; MEASURING ; METALLURGY ; MICROBIOLOGY ; MICROORGANISMS OR ENZYMES ; MUTATION OR GENETIC ENGINEERING ; NUCLEIC ACIDS ; NUCLEOSIDES ; NUCLEOTIDES ; ORGANIC CHEMISTRY ; PEPTIDES ; PHYSICS ; PROCESSES USING MICROORGANISMS ; PROPAGATING, PRESERVING OR MAINTAINING MICROORGANISMS ; SPIRITS ; SUGARS ; TESTING ; VINEGAR ; WINE</subject><creationdate>2010</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20100129&DB=EPODOC&CC=HK&NR=1131637A1$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76289</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20100129&DB=EPODOC&CC=HK&NR=1131637A1$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>JOHNSON, KEVIN STUART</creatorcontrib><creatorcontrib>POPE, ANTHONY RICHARD</creatorcontrib><creatorcontrib>CLACKSON, TIMOTHY PIERS</creatorcontrib><creatorcontrib>GRIFFITHS, ANDREW DAVID</creatorcontrib><creatorcontrib>MCCAFFERTY, JOHN</creatorcontrib><creatorcontrib>HOOGENBOOM, HENDRICUS RENERUS JACOBUS MATTHEUS</creatorcontrib><creatorcontrib>JACKSON, RONALD HENRY</creatorcontrib><creatorcontrib>CHISWELL, DAVID JOHN</creatorcontrib><creatorcontrib>WINTER, GREGORY PAUL</creatorcontrib><creatorcontrib>BONNERT, TIMOTHY PETER</creatorcontrib><creatorcontrib>HOLLIGER, KASPAR PHILIPP</creatorcontrib><creatorcontrib>MARKS, JAMES DAVID</creatorcontrib><title>METHODS FOR PRODUCING MEMBERS OF SPECIFIC BINDING PAIRS</title><description>A member of a specific binding pair (sbp) is identified by expressing DNA encoding a genetically diverse population of such sbp members in recombinant host cells in which the sbp members are displayed in functional form at the surface of a secreted recombinant genetic display package (rgdp) containing DNA encoding the sbp member or a polypeptide component thereof, by virtue of the sbp member or a polypeptide component thereof being expressed as a fusion with a capsid component of the rgdp. The displayed sbps may be selected by affinity with a complementary sbp member, and the DNA recovered from selected rgdps for expression of the selected sbp members. Antibody sbp members may be thus obtained, with the different chains thereof expressed, one fused to the capsid component and the other in free form for association with the fusion partner polypeptide. A phagemid may be used as an expression vector, with said capsid fusion helping to package the phagemid DNA. Using this method libraries of DNA encoding respective chains of such multimeric sbp members may be combined, thereby obtaining a much greater genetic diversity in the sbp members than could easily be obtained by conventional methods.</description><subject>BEER</subject><subject>BIOCHEMISTRY</subject><subject>CHEMISTRY</subject><subject>COMBINATORIAL CHEMISTRY</subject><subject>COMPOSITIONS THEREOF</subject><subject>CULTURE MEDIA</subject><subject>DERIVATIVES THEREOF</subject><subject>ENZYMOLOGY</subject><subject>FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIREDCHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERSFROM A RACEMIC MIXTURE</subject><subject>INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIRCHEMICAL OR PHYSICAL PROPERTIES</subject><subject>LIBRARIES, e.g. CHEMICAL LIBRARIES, IN SILICOLIBRARIES</subject><subject>MEASURING</subject><subject>METALLURGY</subject><subject>MICROBIOLOGY</subject><subject>MICROORGANISMS OR ENZYMES</subject><subject>MUTATION OR GENETIC ENGINEERING</subject><subject>NUCLEIC ACIDS</subject><subject>NUCLEOSIDES</subject><subject>NUCLEOTIDES</subject><subject>ORGANIC CHEMISTRY</subject><subject>PEPTIDES</subject><subject>PHYSICS</subject><subject>PROCESSES USING MICROORGANISMS</subject><subject>PROPAGATING, PRESERVING OR MAINTAINING MICROORGANISMS</subject><subject>SPIRITS</subject><subject>SUGARS</subject><subject>TESTING</subject><subject>VINEGAR</subject><subject>WINE</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2010</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZDD3dQ3x8HcJVnDzD1IICPJ3CXX29HNX8HX1dXINClbwd1MIDnB19nTzdFZw8vRzAckFOHoGBfMwsKYl5hSn8kJpbgYFN9cQZw_d1IL8-NTigsTk1LzUkngPb0NDY0MzY3NHQ2MilAAA3awnlA</recordid><startdate>20100129</startdate><enddate>20100129</enddate><creator>JOHNSON, KEVIN STUART</creator><creator>POPE, ANTHONY RICHARD</creator><creator>CLACKSON, TIMOTHY PIERS</creator><creator>GRIFFITHS, ANDREW DAVID</creator><creator>MCCAFFERTY, JOHN</creator><creator>HOOGENBOOM, HENDRICUS RENERUS JACOBUS MATTHEUS</creator><creator>JACKSON, RONALD HENRY</creator><creator>CHISWELL, DAVID JOHN</creator><creator>WINTER, GREGORY PAUL</creator><creator>BONNERT, TIMOTHY PETER</creator><creator>HOLLIGER, KASPAR PHILIPP</creator><creator>MARKS, JAMES DAVID</creator><scope>EVB</scope></search><sort><creationdate>20100129</creationdate><title>METHODS FOR PRODUCING MEMBERS OF SPECIFIC BINDING PAIRS</title><author>JOHNSON, KEVIN STUART ; POPE, ANTHONY RICHARD ; CLACKSON, TIMOTHY PIERS ; GRIFFITHS, ANDREW DAVID ; MCCAFFERTY, JOHN ; HOOGENBOOM, HENDRICUS RENERUS JACOBUS MATTHEUS ; JACKSON, RONALD HENRY ; CHISWELL, DAVID JOHN ; WINTER, GREGORY PAUL ; BONNERT, TIMOTHY PETER ; HOLLIGER, KASPAR PHILIPP ; MARKS, JAMES DAVID</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_HK1131637A13</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>2010</creationdate><topic>BEER</topic><topic>BIOCHEMISTRY</topic><topic>CHEMISTRY</topic><topic>COMBINATORIAL CHEMISTRY</topic><topic>COMPOSITIONS THEREOF</topic><topic>CULTURE MEDIA</topic><topic>DERIVATIVES THEREOF</topic><topic>ENZYMOLOGY</topic><topic>FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIREDCHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERSFROM A RACEMIC MIXTURE</topic><topic>INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIRCHEMICAL OR PHYSICAL PROPERTIES</topic><topic>LIBRARIES, e.g. CHEMICAL LIBRARIES, IN SILICOLIBRARIES</topic><topic>MEASURING</topic><topic>METALLURGY</topic><topic>MICROBIOLOGY</topic><topic>MICROORGANISMS OR ENZYMES</topic><topic>MUTATION OR GENETIC ENGINEERING</topic><topic>NUCLEIC ACIDS</topic><topic>NUCLEOSIDES</topic><topic>NUCLEOTIDES</topic><topic>ORGANIC CHEMISTRY</topic><topic>PEPTIDES</topic><topic>PHYSICS</topic><topic>PROCESSES USING MICROORGANISMS</topic><topic>PROPAGATING, PRESERVING OR MAINTAINING MICROORGANISMS</topic><topic>SPIRITS</topic><topic>SUGARS</topic><topic>TESTING</topic><topic>VINEGAR</topic><topic>WINE</topic><toplevel>online_resources</toplevel><creatorcontrib>JOHNSON, KEVIN STUART</creatorcontrib><creatorcontrib>POPE, ANTHONY RICHARD</creatorcontrib><creatorcontrib>CLACKSON, TIMOTHY PIERS</creatorcontrib><creatorcontrib>GRIFFITHS, ANDREW DAVID</creatorcontrib><creatorcontrib>MCCAFFERTY, JOHN</creatorcontrib><creatorcontrib>HOOGENBOOM, HENDRICUS RENERUS JACOBUS MATTHEUS</creatorcontrib><creatorcontrib>JACKSON, RONALD HENRY</creatorcontrib><creatorcontrib>CHISWELL, DAVID JOHN</creatorcontrib><creatorcontrib>WINTER, GREGORY PAUL</creatorcontrib><creatorcontrib>BONNERT, TIMOTHY PETER</creatorcontrib><creatorcontrib>HOLLIGER, KASPAR PHILIPP</creatorcontrib><creatorcontrib>MARKS, JAMES DAVID</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>JOHNSON, KEVIN STUART</au><au>POPE, ANTHONY RICHARD</au><au>CLACKSON, TIMOTHY PIERS</au><au>GRIFFITHS, ANDREW DAVID</au><au>MCCAFFERTY, JOHN</au><au>HOOGENBOOM, HENDRICUS RENERUS JACOBUS MATTHEUS</au><au>JACKSON, RONALD HENRY</au><au>CHISWELL, DAVID JOHN</au><au>WINTER, GREGORY PAUL</au><au>BONNERT, TIMOTHY PETER</au><au>HOLLIGER, KASPAR PHILIPP</au><au>MARKS, JAMES DAVID</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>METHODS FOR PRODUCING MEMBERS OF SPECIFIC BINDING PAIRS</title><date>2010-01-29</date><risdate>2010</risdate><abstract>A member of a specific binding pair (sbp) is identified by expressing DNA encoding a genetically diverse population of such sbp members in recombinant host cells in which the sbp members are displayed in functional form at the surface of a secreted recombinant genetic display package (rgdp) containing DNA encoding the sbp member or a polypeptide component thereof, by virtue of the sbp member or a polypeptide component thereof being expressed as a fusion with a capsid component of the rgdp. The displayed sbps may be selected by affinity with a complementary sbp member, and the DNA recovered from selected rgdps for expression of the selected sbp members. Antibody sbp members may be thus obtained, with the different chains thereof expressed, one fused to the capsid component and the other in free form for association with the fusion partner polypeptide. A phagemid may be used as an expression vector, with said capsid fusion helping to package the phagemid DNA. Using this method libraries of DNA encoding respective chains of such multimeric sbp members may be combined, thereby obtaining a much greater genetic diversity in the sbp members than could easily be obtained by conventional methods.</abstract><oa>free_for_read</oa></addata></record> |
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subjects | BEER BIOCHEMISTRY CHEMISTRY COMBINATORIAL CHEMISTRY COMPOSITIONS THEREOF CULTURE MEDIA DERIVATIVES THEREOF ENZYMOLOGY FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIREDCHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERSFROM A RACEMIC MIXTURE INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIRCHEMICAL OR PHYSICAL PROPERTIES LIBRARIES, e.g. CHEMICAL LIBRARIES, IN SILICOLIBRARIES MEASURING METALLURGY MICROBIOLOGY MICROORGANISMS OR ENZYMES MUTATION OR GENETIC ENGINEERING NUCLEIC ACIDS NUCLEOSIDES NUCLEOTIDES ORGANIC CHEMISTRY PEPTIDES PHYSICS PROCESSES USING MICROORGANISMS PROPAGATING, PRESERVING OR MAINTAINING MICROORGANISMS SPIRITS SUGARS TESTING VINEGAR WINE |
title | METHODS FOR PRODUCING MEMBERS OF SPECIFIC BINDING PAIRS |
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