Screening of scFv-displaying phages recognizing distinct extracellular domains of EGF receptor by target-guided proximity labeling method
We recently constructed the scFv-displaying phage library with extremely high repertoire and have successfully utilized for screening scFv antibodies against various proteins, polysaccharides and glyco-lipids. Here, we developed a new screening strategy to isolate scFv antibodies against cell surfac...
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creator | Chang, Chialun Takayanagi, Atsushi Yoshida, Tetsuhiko Shimizu, Nobuyoshi |
description | We recently constructed the scFv-displaying phage library with extremely high repertoire and have successfully utilized for screening scFv antibodies against various proteins, polysaccharides and glyco-lipids. Here, we developed a new screening strategy to isolate scFv antibodies against cell surface EGF receptor (EGFR). For this, we applied two slightly different methods of “target-guided proximity labeling,” such as Proximity selection (ProxiMol) method and a new sulfo-SBED labeling method with the aide of monoclonal anti-human EGFR antibody B4G7 as a guide molecule. ProxiMol method relies on the Biotin-labeling of scFv-displaying phages that bound to the target in a vicinity of 100
Å from the guide molecule, whereas sulfo-SBED method transfers Biotin to scFv-displaying phages, which bound to the target in a distance of 20
Å. After two rounds of panning on the EGFR-overexpressing A431 cells starting from approx. 1
×
10
12
pfu, 47 each of Biotin-labeled scFv-displaying phages were recovered using Streptoavidin-coated magnetic beads, and among them total 11 scFv-phages were found to be definitely positive for binding to A431 cell surface by ELISA assay. Restriction mapping and sequencing analysis of these scFv-phage DNAs revealed that they encode 4 different scFv-nucleotide sequences in total. Immuno-fluorescent microscopy provided evidence that these 4 scFv antibodies bind specifically to EGFR on the A431 cells, showing slightly different staining patterns. Thus, “target-guided proximity labeling” methods were powerful for isolating scFv-displaying phages that recognize distinct extracellular domains of the target receptor. This novel screening strategy could be applicable to many other cell surface antigens and receptors.
► Four distinct scFv antibodies against human EGF receptor were isolated. ► Our original antibody-displaying phage library possessed extremely high repertoires. ► Two types of target-guided proximity labeling methods were used. ► They allowed the isolation of scFv antibodies with different staining patterns. |
doi_str_mv | 10.1016/j.jim.2011.07.003 |
format | Article |
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Å from the guide molecule, whereas sulfo-SBED method transfers Biotin to scFv-displaying phages, which bound to the target in a distance of 20
Å. After two rounds of panning on the EGFR-overexpressing A431 cells starting from approx. 1
×
10
12
pfu, 47 each of Biotin-labeled scFv-displaying phages were recovered using Streptoavidin-coated magnetic beads, and among them total 11 scFv-phages were found to be definitely positive for binding to A431 cell surface by ELISA assay. Restriction mapping and sequencing analysis of these scFv-phage DNAs revealed that they encode 4 different scFv-nucleotide sequences in total. Immuno-fluorescent microscopy provided evidence that these 4 scFv antibodies bind specifically to EGFR on the A431 cells, showing slightly different staining patterns. Thus, “target-guided proximity labeling” methods were powerful for isolating scFv-displaying phages that recognize distinct extracellular domains of the target receptor. This novel screening strategy could be applicable to many other cell surface antigens and receptors.
► Four distinct scFv antibodies against human EGF receptor were isolated. ► Our original antibody-displaying phage library possessed extremely high repertoires. ► Two types of target-guided proximity labeling methods were used. ► They allowed the isolation of scFv antibodies with different staining patterns.</description><identifier>ISSN: 0022-1759</identifier><identifier>EISSN: 1872-7905</identifier><identifier>DOI: 10.1016/j.jim.2011.07.003</identifier><identifier>PMID: 21782821</identifier><identifier>CODEN: JIMMBG</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>antibodies ; Antibody screening ; Antibody Specificity ; bacteriophages ; Biological and medical sciences ; Biotin ; Cell Line, Tumor ; Cloning, Molecular ; DNA libraries ; EGF receptor ; enzyme-linked immunosorbent assay ; epidermal growth factor receptors ; Epitopes - immunology ; Fundamental and applied biological sciences. Psychology ; Fundamental immunology ; Humans ; Immunoglobulin Fragments - genetics ; Immunoglobulin Fragments - immunology ; Microbiology ; microscopy ; Molecular immunology ; Peptide Library ; Phage display ; polysaccharides ; Receptor, Epidermal Growth Factor - immunology ; restriction mapping ; screening ; sequence analysis ; Single-Chain Antibodies - immunology ; surface antigens ; Techniques ; Techniques used in virology ; Virology</subject><ispartof>Journal of immunological methods, 2011-09, Vol.372 (1), p.127-136</ispartof><rights>2011</rights><rights>2015 INIST-CNRS</rights><rights>Crown Copyright © 2011. Published by Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c504t-660de873d69d099b94d9aa534d5cce5570ed88260c3e986aa542e5e0fe87f1c33</citedby><cites>FETCH-LOGICAL-c504t-660de873d69d099b94d9aa534d5cce5570ed88260c3e986aa542e5e0fe87f1c33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jim.2011.07.003$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27926,27927,45997</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24560008$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21782821$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chang, Chialun</creatorcontrib><creatorcontrib>Takayanagi, Atsushi</creatorcontrib><creatorcontrib>Yoshida, Tetsuhiko</creatorcontrib><creatorcontrib>Shimizu, Nobuyoshi</creatorcontrib><title>Screening of scFv-displaying phages recognizing distinct extracellular domains of EGF receptor by target-guided proximity labeling method</title><title>Journal of immunological methods</title><addtitle>J Immunol Methods</addtitle><description>We recently constructed the scFv-displaying phage library with extremely high repertoire and have successfully utilized for screening scFv antibodies against various proteins, polysaccharides and glyco-lipids. Here, we developed a new screening strategy to isolate scFv antibodies against cell surface EGF receptor (EGFR). For this, we applied two slightly different methods of “target-guided proximity labeling,” such as Proximity selection (ProxiMol) method and a new sulfo-SBED labeling method with the aide of monoclonal anti-human EGFR antibody B4G7 as a guide molecule. ProxiMol method relies on the Biotin-labeling of scFv-displaying phages that bound to the target in a vicinity of 100
Å from the guide molecule, whereas sulfo-SBED method transfers Biotin to scFv-displaying phages, which bound to the target in a distance of 20
Å. After two rounds of panning on the EGFR-overexpressing A431 cells starting from approx. 1
×
10
12
pfu, 47 each of Biotin-labeled scFv-displaying phages were recovered using Streptoavidin-coated magnetic beads, and among them total 11 scFv-phages were found to be definitely positive for binding to A431 cell surface by ELISA assay. Restriction mapping and sequencing analysis of these scFv-phage DNAs revealed that they encode 4 different scFv-nucleotide sequences in total. Immuno-fluorescent microscopy provided evidence that these 4 scFv antibodies bind specifically to EGFR on the A431 cells, showing slightly different staining patterns. Thus, “target-guided proximity labeling” methods were powerful for isolating scFv-displaying phages that recognize distinct extracellular domains of the target receptor. This novel screening strategy could be applicable to many other cell surface antigens and receptors.
► Four distinct scFv antibodies against human EGF receptor were isolated. ► Our original antibody-displaying phage library possessed extremely high repertoires. ► Two types of target-guided proximity labeling methods were used. ► They allowed the isolation of scFv antibodies with different staining patterns.</description><subject>antibodies</subject><subject>Antibody screening</subject><subject>Antibody Specificity</subject><subject>bacteriophages</subject><subject>Biological and medical sciences</subject><subject>Biotin</subject><subject>Cell Line, Tumor</subject><subject>Cloning, Molecular</subject><subject>DNA libraries</subject><subject>EGF receptor</subject><subject>enzyme-linked immunosorbent assay</subject><subject>epidermal growth factor receptors</subject><subject>Epitopes - immunology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fundamental immunology</subject><subject>Humans</subject><subject>Immunoglobulin Fragments - genetics</subject><subject>Immunoglobulin Fragments - immunology</subject><subject>Microbiology</subject><subject>microscopy</subject><subject>Molecular immunology</subject><subject>Peptide Library</subject><subject>Phage display</subject><subject>polysaccharides</subject><subject>Receptor, Epidermal Growth Factor - immunology</subject><subject>restriction mapping</subject><subject>screening</subject><subject>sequence analysis</subject><subject>Single-Chain Antibodies - immunology</subject><subject>surface antigens</subject><subject>Techniques</subject><subject>Techniques used in virology</subject><subject>Virology</subject><issn>0022-1759</issn><issn>1872-7905</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1v1DAQhiMEotvCD-ACuSBOCeMk_hInVHULUiUOpWfLa09Sr_KF7VRd_gH_Gke7hRucLM0873jsJ8veECgJEPZxX-7dUFZASAm8BKifZRsieFVwCfR5tgGoqoJwKs-y8xD2AECAwcvsrCJcVKIim-zXrfGIoxu7fGrzYLYPhXVh7vVhLc33usOQezRTN7qfayl1oxtNzPExem2w75de-9xOg3ZjWIdcXW_XBM5x8vnukEftO4xFtziLNp_99OgGFw95r3fYryMHjPeTfZW9aHUf8PXpvMjutlffL78UN9-uv15-vikMhSYWjIFFwWvLpAUpd7KxUmtaN5Yag5RyQCtExcDUKAVLraZCitCmUEtMXV9kH45z0yY_FgxRDS6s79AjTktQEppGEsn-Twoh6gaAkUSSI2n8FILHVs3eDdofFAG1qlJ7lVSpVZUCrpKqlHl7mr7sBrR_Ek9uEvD-BOhgdN96PRoX_nINZcmoSNy7I9fqSenOJ-buNt1Ek27OKWGJ-HQkMP3rg0OvgnE4GrQuiYrKTu4fi_4GtzK8mw</recordid><startdate>20110930</startdate><enddate>20110930</enddate><creator>Chang, Chialun</creator><creator>Takayanagi, Atsushi</creator><creator>Yoshida, Tetsuhiko</creator><creator>Shimizu, Nobuyoshi</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>FBQ</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7T5</scope><scope>H94</scope></search><sort><creationdate>20110930</creationdate><title>Screening of scFv-displaying phages recognizing distinct extracellular domains of EGF receptor by target-guided proximity labeling method</title><author>Chang, Chialun ; Takayanagi, Atsushi ; Yoshida, Tetsuhiko ; Shimizu, Nobuyoshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c504t-660de873d69d099b94d9aa534d5cce5570ed88260c3e986aa542e5e0fe87f1c33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>antibodies</topic><topic>Antibody screening</topic><topic>Antibody Specificity</topic><topic>bacteriophages</topic><topic>Biological and medical sciences</topic><topic>Biotin</topic><topic>Cell Line, Tumor</topic><topic>Cloning, Molecular</topic><topic>DNA libraries</topic><topic>EGF receptor</topic><topic>enzyme-linked immunosorbent assay</topic><topic>epidermal growth factor receptors</topic><topic>Epitopes - immunology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fundamental immunology</topic><topic>Humans</topic><topic>Immunoglobulin Fragments - genetics</topic><topic>Immunoglobulin Fragments - immunology</topic><topic>Microbiology</topic><topic>microscopy</topic><topic>Molecular immunology</topic><topic>Peptide Library</topic><topic>Phage display</topic><topic>polysaccharides</topic><topic>Receptor, Epidermal Growth Factor - immunology</topic><topic>restriction mapping</topic><topic>screening</topic><topic>sequence analysis</topic><topic>Single-Chain Antibodies - immunology</topic><topic>surface antigens</topic><topic>Techniques</topic><topic>Techniques used in virology</topic><topic>Virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chang, Chialun</creatorcontrib><creatorcontrib>Takayanagi, Atsushi</creatorcontrib><creatorcontrib>Yoshida, Tetsuhiko</creatorcontrib><creatorcontrib>Shimizu, Nobuyoshi</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Journal of immunological methods</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chang, Chialun</au><au>Takayanagi, Atsushi</au><au>Yoshida, Tetsuhiko</au><au>Shimizu, Nobuyoshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Screening of scFv-displaying phages recognizing distinct extracellular domains of EGF receptor by target-guided proximity labeling method</atitle><jtitle>Journal of immunological methods</jtitle><addtitle>J Immunol Methods</addtitle><date>2011-09-30</date><risdate>2011</risdate><volume>372</volume><issue>1</issue><spage>127</spage><epage>136</epage><pages>127-136</pages><issn>0022-1759</issn><eissn>1872-7905</eissn><coden>JIMMBG</coden><abstract>We recently constructed the scFv-displaying phage library with extremely high repertoire and have successfully utilized for screening scFv antibodies against various proteins, polysaccharides and glyco-lipids. Here, we developed a new screening strategy to isolate scFv antibodies against cell surface EGF receptor (EGFR). For this, we applied two slightly different methods of “target-guided proximity labeling,” such as Proximity selection (ProxiMol) method and a new sulfo-SBED labeling method with the aide of monoclonal anti-human EGFR antibody B4G7 as a guide molecule. ProxiMol method relies on the Biotin-labeling of scFv-displaying phages that bound to the target in a vicinity of 100
Å from the guide molecule, whereas sulfo-SBED method transfers Biotin to scFv-displaying phages, which bound to the target in a distance of 20
Å. After two rounds of panning on the EGFR-overexpressing A431 cells starting from approx. 1
×
10
12
pfu, 47 each of Biotin-labeled scFv-displaying phages were recovered using Streptoavidin-coated magnetic beads, and among them total 11 scFv-phages were found to be definitely positive for binding to A431 cell surface by ELISA assay. Restriction mapping and sequencing analysis of these scFv-phage DNAs revealed that they encode 4 different scFv-nucleotide sequences in total. Immuno-fluorescent microscopy provided evidence that these 4 scFv antibodies bind specifically to EGFR on the A431 cells, showing slightly different staining patterns. Thus, “target-guided proximity labeling” methods were powerful for isolating scFv-displaying phages that recognize distinct extracellular domains of the target receptor. This novel screening strategy could be applicable to many other cell surface antigens and receptors.
► Four distinct scFv antibodies against human EGF receptor were isolated. ► Our original antibody-displaying phage library possessed extremely high repertoires. ► Two types of target-guided proximity labeling methods were used. ► They allowed the isolation of scFv antibodies with different staining patterns.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>21782821</pmid><doi>10.1016/j.jim.2011.07.003</doi><tpages>10</tpages></addata></record> |
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subjects | antibodies Antibody screening Antibody Specificity bacteriophages Biological and medical sciences Biotin Cell Line, Tumor Cloning, Molecular DNA libraries EGF receptor enzyme-linked immunosorbent assay epidermal growth factor receptors Epitopes - immunology Fundamental and applied biological sciences. Psychology Fundamental immunology Humans Immunoglobulin Fragments - genetics Immunoglobulin Fragments - immunology Microbiology microscopy Molecular immunology Peptide Library Phage display polysaccharides Receptor, Epidermal Growth Factor - immunology restriction mapping screening sequence analysis Single-Chain Antibodies - immunology surface antigens Techniques Techniques used in virology Virology |
title | Screening of scFv-displaying phages recognizing distinct extracellular domains of EGF receptor by target-guided proximity labeling method |
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