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Generation, characterization, and docking studies of DNA-hydrolyzing recombinant Fab antibodies
Previously we established a series of catalytic antibodies (catAbs) capable of hydrolyzing DNA prepared by hybridoma technology. A group of these catAbs exhibited high reactivity and substrate specificity. To determine the molecular basis for these catAbs, we cloned, sequenced, and expressed the var...
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Published in: | Journal of molecular recognition 2011-09, Vol.24 (5), p.862-874 |
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creator | Zein, Haggag S. El-Sehemy, Ahmed A. Fares, Mohamed O. ElHefnawi, Mahmoud Teixeira da Silva, Jaime A. Miyatake, Kazutaka |
description | Previously we established a series of catalytic antibodies (catAbs) capable of hydrolyzing DNA prepared by hybridoma technology. A group of these catAbs exhibited high reactivity and substrate specificity. To determine the molecular basis for these catAbs, we cloned, sequenced, and expressed the variable regions of this group of antibodies as functional Fab fragments. The nucleotide and deduced amino acid sequences of the expressed light chain (Vκ) germline gene assignments confidently belonged to germline family Vκ1A, gene bb1.1 and GenBank accession number EF672207 while heavy chain variable region VH genes belonged to VH1/VHJ558, gene V130.3 and GenBank accession number EF672221. A well‐established expression system based on the pARA7 vector was examined for its ability to produce catalytically active antibodies. Recombinant Fab (rFab) fragments were purified and their hydrolyzing activity was analyzed against supercoiled pUC19 plasmid DNA (scDNA). The study of rFab provides important information about the potential catalytic activities of antibodies whose structure allows us to understand their basis of catalysis. Molecular surface analysis and docking studies were performed on the molecular interactions between the antibodies and poly(dA9), poly(dG9), poly(dT9), and poly(dC9) oligomers. Surface analysis identified the important sequence motifs at the binding sites, and different effects exerted by arginine and tyrosine residues at different positions in the light and heavy chains. This study demonstrates the potential usefulness of the protein DNA surrogate in the investigation of the origin of anti‐DNA antibodies. These studies may define important features of DNA catAbs. Copyright © 2011 John Wiley & Sons, Ltd. |
doi_str_mv | 10.1002/jmr.1129 |
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A group of these catAbs exhibited high reactivity and substrate specificity. To determine the molecular basis for these catAbs, we cloned, sequenced, and expressed the variable regions of this group of antibodies as functional Fab fragments. The nucleotide and deduced amino acid sequences of the expressed light chain (Vκ) germline gene assignments confidently belonged to germline family Vκ1A, gene bb1.1 and GenBank accession number EF672207 while heavy chain variable region VH genes belonged to VH1/VHJ558, gene V130.3 and GenBank accession number EF672221. A well‐established expression system based on the pARA7 vector was examined for its ability to produce catalytically active antibodies. Recombinant Fab (rFab) fragments were purified and their hydrolyzing activity was analyzed against supercoiled pUC19 plasmid DNA (scDNA). The study of rFab provides important information about the potential catalytic activities of antibodies whose structure allows us to understand their basis of catalysis. Molecular surface analysis and docking studies were performed on the molecular interactions between the antibodies and poly(dA9), poly(dG9), poly(dT9), and poly(dC9) oligomers. Surface analysis identified the important sequence motifs at the binding sites, and different effects exerted by arginine and tyrosine residues at different positions in the light and heavy chains. This study demonstrates the potential usefulness of the protein DNA surrogate in the investigation of the origin of anti‐DNA antibodies. These studies may define important features of DNA catAbs. Copyright © 2011 John Wiley & Sons, Ltd.</description><identifier>ISSN: 0952-3499</identifier><identifier>ISSN: 1099-1352</identifier><identifier>EISSN: 1099-1352</identifier><identifier>DOI: 10.1002/jmr.1129</identifier><language>eng</language><publisher>Chichester, UK: John Wiley & Sons, Ltd</publisher><subject>catalytic antibodies ; DNA-antibody docking ; Fab fragments ; immunoglobulin genes ; molecular surface analysis ; single-chain antibody</subject><ispartof>Journal of molecular recognition, 2011-09, Vol.24 (5), p.862-874</ispartof><rights>Copyright © 2011 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Zein, Haggag S.</creatorcontrib><creatorcontrib>El-Sehemy, Ahmed A.</creatorcontrib><creatorcontrib>Fares, Mohamed O.</creatorcontrib><creatorcontrib>ElHefnawi, Mahmoud</creatorcontrib><creatorcontrib>Teixeira da Silva, Jaime A.</creatorcontrib><creatorcontrib>Miyatake, Kazutaka</creatorcontrib><title>Generation, characterization, and docking studies of DNA-hydrolyzing recombinant Fab antibodies</title><title>Journal of molecular recognition</title><addtitle>J. Mol. Recognit</addtitle><description>Previously we established a series of catalytic antibodies (catAbs) capable of hydrolyzing DNA prepared by hybridoma technology. A group of these catAbs exhibited high reactivity and substrate specificity. To determine the molecular basis for these catAbs, we cloned, sequenced, and expressed the variable regions of this group of antibodies as functional Fab fragments. The nucleotide and deduced amino acid sequences of the expressed light chain (Vκ) germline gene assignments confidently belonged to germline family Vκ1A, gene bb1.1 and GenBank accession number EF672207 while heavy chain variable region VH genes belonged to VH1/VHJ558, gene V130.3 and GenBank accession number EF672221. A well‐established expression system based on the pARA7 vector was examined for its ability to produce catalytically active antibodies. Recombinant Fab (rFab) fragments were purified and their hydrolyzing activity was analyzed against supercoiled pUC19 plasmid DNA (scDNA). The study of rFab provides important information about the potential catalytic activities of antibodies whose structure allows us to understand their basis of catalysis. Molecular surface analysis and docking studies were performed on the molecular interactions between the antibodies and poly(dA9), poly(dG9), poly(dT9), and poly(dC9) oligomers. Surface analysis identified the important sequence motifs at the binding sites, and different effects exerted by arginine and tyrosine residues at different positions in the light and heavy chains. This study demonstrates the potential usefulness of the protein DNA surrogate in the investigation of the origin of anti‐DNA antibodies. These studies may define important features of DNA catAbs. Copyright © 2011 John Wiley & Sons, Ltd.</description><subject>catalytic antibodies</subject><subject>DNA-antibody docking</subject><subject>Fab fragments</subject><subject>immunoglobulin genes</subject><subject>molecular surface analysis</subject><subject>single-chain antibody</subject><issn>0952-3499</issn><issn>1099-1352</issn><issn>1099-1352</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNpFkF1PwjAYhRujiYgm_oRdeuGwn9t6iSigQTSK8bLp1k4K24rtiI5f7xaIXp3kPc95Lx4ALhEcIAjxzap0A4QwPwI9BDkPEWH4GPQgZzgklPNTcOb9CsK2Y7AHxERX2sna2Oo6yJbSyazWzuwOF1mpQNlsbarPwNdbZbQPbB7czYfhslHOFs2uq5zObJmaSlZ1MJZpO6tNajv6HJzksvD64pB98D6-X4ym4ex58jAazkKDOOUhiSniitAkzRREEuWY5IRijSOtIh7FOGGSKY5zGiOeR3EmkSZKYYUxJRxR0gdX-78bZ7-22teiND7TRSErbbdeIIhhQlmCkxYN9-i3KXQjNs6U0jUtITqBohUoOoHi8em1y3_e-Fr__PHSrUUUk5iJj_lERIuI0enti3gjv7RrdCM</recordid><startdate>201109</startdate><enddate>201109</enddate><creator>Zein, Haggag S.</creator><creator>El-Sehemy, Ahmed A.</creator><creator>Fares, Mohamed O.</creator><creator>ElHefnawi, Mahmoud</creator><creator>Teixeira da Silva, Jaime A.</creator><creator>Miyatake, Kazutaka</creator><general>John Wiley & Sons, Ltd</general><scope>BSCLL</scope><scope>7TM</scope></search><sort><creationdate>201109</creationdate><title>Generation, characterization, and docking studies of DNA-hydrolyzing recombinant Fab antibodies</title><author>Zein, Haggag S. ; El-Sehemy, Ahmed A. ; Fares, Mohamed O. ; ElHefnawi, Mahmoud ; Teixeira da Silva, Jaime A. ; Miyatake, Kazutaka</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i1949-37419d348bcd01a1f23f342e26ed6967285a5d92f4719f67ca1e3dd2d22439143</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>catalytic antibodies</topic><topic>DNA-antibody docking</topic><topic>Fab fragments</topic><topic>immunoglobulin genes</topic><topic>molecular surface analysis</topic><topic>single-chain antibody</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zein, Haggag S.</creatorcontrib><creatorcontrib>El-Sehemy, Ahmed A.</creatorcontrib><creatorcontrib>Fares, Mohamed O.</creatorcontrib><creatorcontrib>ElHefnawi, Mahmoud</creatorcontrib><creatorcontrib>Teixeira da Silva, Jaime A.</creatorcontrib><creatorcontrib>Miyatake, Kazutaka</creatorcontrib><collection>Istex</collection><collection>Nucleic Acids Abstracts</collection><jtitle>Journal of molecular recognition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zein, Haggag S.</au><au>El-Sehemy, Ahmed A.</au><au>Fares, Mohamed O.</au><au>ElHefnawi, Mahmoud</au><au>Teixeira da Silva, Jaime A.</au><au>Miyatake, Kazutaka</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Generation, characterization, and docking studies of DNA-hydrolyzing recombinant Fab antibodies</atitle><jtitle>Journal of molecular recognition</jtitle><addtitle>J. Mol. Recognit</addtitle><date>2011-09</date><risdate>2011</risdate><volume>24</volume><issue>5</issue><spage>862</spage><epage>874</epage><pages>862-874</pages><issn>0952-3499</issn><issn>1099-1352</issn><eissn>1099-1352</eissn><abstract>Previously we established a series of catalytic antibodies (catAbs) capable of hydrolyzing DNA prepared by hybridoma technology. A group of these catAbs exhibited high reactivity and substrate specificity. To determine the molecular basis for these catAbs, we cloned, sequenced, and expressed the variable regions of this group of antibodies as functional Fab fragments. The nucleotide and deduced amino acid sequences of the expressed light chain (Vκ) germline gene assignments confidently belonged to germline family Vκ1A, gene bb1.1 and GenBank accession number EF672207 while heavy chain variable region VH genes belonged to VH1/VHJ558, gene V130.3 and GenBank accession number EF672221. A well‐established expression system based on the pARA7 vector was examined for its ability to produce catalytically active antibodies. Recombinant Fab (rFab) fragments were purified and their hydrolyzing activity was analyzed against supercoiled pUC19 plasmid DNA (scDNA). The study of rFab provides important information about the potential catalytic activities of antibodies whose structure allows us to understand their basis of catalysis. Molecular surface analysis and docking studies were performed on the molecular interactions between the antibodies and poly(dA9), poly(dG9), poly(dT9), and poly(dC9) oligomers. Surface analysis identified the important sequence motifs at the binding sites, and different effects exerted by arginine and tyrosine residues at different positions in the light and heavy chains. This study demonstrates the potential usefulness of the protein DNA surrogate in the investigation of the origin of anti‐DNA antibodies. These studies may define important features of DNA catAbs. Copyright © 2011 John Wiley & Sons, Ltd.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><doi>10.1002/jmr.1129</doi><tpages>13</tpages></addata></record> |
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subjects | catalytic antibodies DNA-antibody docking Fab fragments immunoglobulin genes molecular surface analysis single-chain antibody |
title | Generation, characterization, and docking studies of DNA-hydrolyzing recombinant Fab antibodies |
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