Production and Characterization of Monoclonal Antibody Broadly Recognizing Cry1 Toxins by Use of Designed Polypeptide as Hapten
In this study, by use of synthesized polypeptides as haptens, a monoclonal antibody with broad recognition against seven major Cry1 toxins (Cry1Aa, Cry1Ab, Cry1Ac, Cry1B, Cry1C, Cry1E, and Cry1F) has been produced and characterized. First, by comparing the three-dimensional structures of seven Cry1...
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creator | Dong, Sa Zhang, Cunzheng Zhang, Xiao Liu, Yuan Zhong, Jianfeng Xie, Yajing Xu, Chongxin Ding, Ying Zhang, Liuquan Liu, Xianjin |
description | In this study, by use of synthesized polypeptides as haptens, a monoclonal antibody with broad recognition against seven major Cry1 toxins (Cry1Aa, Cry1Ab, Cry1Ac, Cry1B, Cry1C, Cry1E, and Cry1F) has been produced and characterized. First, by comparing the three-dimensional structures of seven Cry1 toxins, analyzing the conserved sequences, and considering the antigenicity and hydrophilicity, three polypeptides (T1, T2, and T3) have been chosen and coupled to keyhole limpet hemocyanin as immunogens for the generic monoclonal antibody (Mab) generation. Thereafter, a double antibody sandwich enzyme-linked immunosorbent assay method (DAS-ELISA) was developed for simultaneous determination of seven Cry1 toxins. The results revealed that the haptens T1, T2, and T3 had different effects in the production of antibodies. Among them, the obtained Mab (strain 2D3) generated by T2 can recognize seven Cry1 toxins simultaneously. Equilibrium dissociation constant (K D) values for seven Cry1 toxins with Mab 2D3 were 1.198 × 10–8 M for Cry1Aa, 2.197 × 10–8 M for Cry1Ab, 1.367 × 10–8 M for Cry1Ac, 2.092 × 10–8 M for Cry1B, 5.177 × 10–8 M for Cry1C, 4.016 × 10–8 M for Cry1E, and 3.497 × 10–8 M for Cry1F. For 2D3-based DAS-ELISA, the limits of detection (LOD) and limits of quantification (LOQ) can reach 15 and 30 ng·mL–1 for each Cry1 toxin, respectively. Our study is the first report of a broadly specific immunoassay for multidetermination of seven major Cry1 toxins, and it will provide a new idea and technical routes for development of multidetermination immunoassays. |
doi_str_mv | 10.1021/acs.analchem.6b00429 |
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First, by comparing the three-dimensional structures of seven Cry1 toxins, analyzing the conserved sequences, and considering the antigenicity and hydrophilicity, three polypeptides (T1, T2, and T3) have been chosen and coupled to keyhole limpet hemocyanin as immunogens for the generic monoclonal antibody (Mab) generation. Thereafter, a double antibody sandwich enzyme-linked immunosorbent assay method (DAS-ELISA) was developed for simultaneous determination of seven Cry1 toxins. The results revealed that the haptens T1, T2, and T3 had different effects in the production of antibodies. Among them, the obtained Mab (strain 2D3) generated by T2 can recognize seven Cry1 toxins simultaneously. Equilibrium dissociation constant (K D) values for seven Cry1 toxins with Mab 2D3 were 1.198 × 10–8 M for Cry1Aa, 2.197 × 10–8 M for Cry1Ab, 1.367 × 10–8 M for Cry1Ac, 2.092 × 10–8 M for Cry1B, 5.177 × 10–8 M for Cry1C, 4.016 × 10–8 M for Cry1E, and 3.497 × 10–8 M for Cry1F. For 2D3-based DAS-ELISA, the limits of detection (LOD) and limits of quantification (LOQ) can reach 15 and 30 ng·mL–1 for each Cry1 toxin, respectively. Our study is the first report of a broadly specific immunoassay for multidetermination of seven major Cry1 toxins, and it will provide a new idea and technical routes for development of multidetermination immunoassays.</description><identifier>ISSN: 0003-2700</identifier><identifier>EISSN: 1520-6882</identifier><identifier>DOI: 10.1021/acs.analchem.6b00429</identifier><identifier>PMID: 27341419</identifier><identifier>CODEN: ANCHAM</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Antibodies ; Comparative analysis ; Constants ; Immunoassay ; Joining ; Monoclonal antibodies ; Polypeptides ; Recognition ; Toxins</subject><ispartof>Analytical chemistry (Washington), 2016-07, Vol.88 (14), p.7023-7032</ispartof><rights>Copyright © 2016 American Chemical Society</rights><rights>Copyright American Chemical Society Jul 19, 2016</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a442t-94b0f4979623878e1c08652e100f7bdfd9ba6206870cfa4e43bb89dba0b872db3</citedby><cites>FETCH-LOGICAL-a442t-94b0f4979623878e1c08652e100f7bdfd9ba6206870cfa4e43bb89dba0b872db3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/acs.analchem.6b00429$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acs.analchem.6b00429$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>315,781,785,2766,27081,27929,27930,56743,56793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27341419$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dong, Sa</creatorcontrib><creatorcontrib>Zhang, Cunzheng</creatorcontrib><creatorcontrib>Zhang, Xiao</creatorcontrib><creatorcontrib>Liu, Yuan</creatorcontrib><creatorcontrib>Zhong, Jianfeng</creatorcontrib><creatorcontrib>Xie, Yajing</creatorcontrib><creatorcontrib>Xu, Chongxin</creatorcontrib><creatorcontrib>Ding, Ying</creatorcontrib><creatorcontrib>Zhang, Liuquan</creatorcontrib><creatorcontrib>Liu, Xianjin</creatorcontrib><title>Production and Characterization of Monoclonal Antibody Broadly Recognizing Cry1 Toxins by Use of Designed Polypeptide as Hapten</title><title>Analytical chemistry (Washington)</title><addtitle>Anal. Chem</addtitle><description>In this study, by use of synthesized polypeptides as haptens, a monoclonal antibody with broad recognition against seven major Cry1 toxins (Cry1Aa, Cry1Ab, Cry1Ac, Cry1B, Cry1C, Cry1E, and Cry1F) has been produced and characterized. First, by comparing the three-dimensional structures of seven Cry1 toxins, analyzing the conserved sequences, and considering the antigenicity and hydrophilicity, three polypeptides (T1, T2, and T3) have been chosen and coupled to keyhole limpet hemocyanin as immunogens for the generic monoclonal antibody (Mab) generation. Thereafter, a double antibody sandwich enzyme-linked immunosorbent assay method (DAS-ELISA) was developed for simultaneous determination of seven Cry1 toxins. The results revealed that the haptens T1, T2, and T3 had different effects in the production of antibodies. Among them, the obtained Mab (strain 2D3) generated by T2 can recognize seven Cry1 toxins simultaneously. Equilibrium dissociation constant (K D) values for seven Cry1 toxins with Mab 2D3 were 1.198 × 10–8 M for Cry1Aa, 2.197 × 10–8 M for Cry1Ab, 1.367 × 10–8 M for Cry1Ac, 2.092 × 10–8 M for Cry1B, 5.177 × 10–8 M for Cry1C, 4.016 × 10–8 M for Cry1E, and 3.497 × 10–8 M for Cry1F. For 2D3-based DAS-ELISA, the limits of detection (LOD) and limits of quantification (LOQ) can reach 15 and 30 ng·mL–1 for each Cry1 toxin, respectively. Our study is the first report of a broadly specific immunoassay for multidetermination of seven major Cry1 toxins, and it will provide a new idea and technical routes for development of multidetermination immunoassays.</description><subject>Antibodies</subject><subject>Comparative analysis</subject><subject>Constants</subject><subject>Immunoassay</subject><subject>Joining</subject><subject>Monoclonal antibodies</subject><subject>Polypeptides</subject><subject>Recognition</subject><subject>Toxins</subject><issn>0003-2700</issn><issn>1520-6882</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqNkUtrFEEURgtRzBj9ByIFbtz0eKu6uh7LOD4iRAySrJt69aRCT1Vb1Q12Nv51e5yJggvJ6sLlfN-FexB6SWBNgJK32pa1jrq3N3635gaAUfUIrUhDoeJS0sdoBQB1RQXACXpWyi0AIUD4U3RCRc0II2qFfl7m5CY7hhSxjg5vbnTWdvQ53Onfy9ThLykm26flFj6LYzDJzfhdTtr1M_7mbdrGcBfiFm_yTPBV-hFiwWbG18Xv0-99CdvoHb5M_Tz4YQzOY13wuR5GH5-jJ53ui39xnKfo-uOHq815dfH10-fN2UWlGaNjpZiBjimhOK2lkJ5YkLyhngB0wrjOKaM5BS4F2E4zz2pjpHJGg5GCOlOfojeH3iGn75MvY7sLxfq-19GnqbRE1k2jFFX8ASghUirByQNQaATnTMgFff0PepumvPz0SEnOlVoodqBsTqVk37VDDjud55ZAu9feLtrbe-3tUfsSe3Usn8zOuz-he88LAAdgH_97-H-dvwC_9bwQ</recordid><startdate>20160719</startdate><enddate>20160719</enddate><creator>Dong, Sa</creator><creator>Zhang, Cunzheng</creator><creator>Zhang, Xiao</creator><creator>Liu, Yuan</creator><creator>Zhong, Jianfeng</creator><creator>Xie, Yajing</creator><creator>Xu, Chongxin</creator><creator>Ding, Ying</creator><creator>Zhang, Liuquan</creator><creator>Liu, Xianjin</creator><general>American Chemical Society</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QF</scope><scope>7QO</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7TA</scope><scope>7TB</scope><scope>7TM</scope><scope>7U5</scope><scope>7U7</scope><scope>7U9</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>H94</scope><scope>JG9</scope><scope>JQ2</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20160719</creationdate><title>Production and Characterization of Monoclonal Antibody Broadly Recognizing Cry1 Toxins by Use of Designed Polypeptide as Hapten</title><author>Dong, Sa ; Zhang, Cunzheng ; Zhang, Xiao ; Liu, Yuan ; Zhong, Jianfeng ; Xie, Yajing ; Xu, Chongxin ; Ding, Ying ; Zhang, Liuquan ; Liu, Xianjin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a442t-94b0f4979623878e1c08652e100f7bdfd9ba6206870cfa4e43bb89dba0b872db3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Antibodies</topic><topic>Comparative analysis</topic><topic>Constants</topic><topic>Immunoassay</topic><topic>Joining</topic><topic>Monoclonal antibodies</topic><topic>Polypeptides</topic><topic>Recognition</topic><topic>Toxins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dong, Sa</creatorcontrib><creatorcontrib>Zhang, Cunzheng</creatorcontrib><creatorcontrib>Zhang, Xiao</creatorcontrib><creatorcontrib>Liu, Yuan</creatorcontrib><creatorcontrib>Zhong, Jianfeng</creatorcontrib><creatorcontrib>Xie, Yajing</creatorcontrib><creatorcontrib>Xu, Chongxin</creatorcontrib><creatorcontrib>Ding, Ying</creatorcontrib><creatorcontrib>Zhang, Liuquan</creatorcontrib><creatorcontrib>Liu, Xianjin</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Aluminium Industry Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Computer and Information Systems Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Materials Business File</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Copper Technical Reference Library</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Computer and Information Systems Abstracts Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Analytical chemistry (Washington)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dong, Sa</au><au>Zhang, Cunzheng</au><au>Zhang, Xiao</au><au>Liu, Yuan</au><au>Zhong, Jianfeng</au><au>Xie, Yajing</au><au>Xu, Chongxin</au><au>Ding, Ying</au><au>Zhang, Liuquan</au><au>Liu, Xianjin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Production and Characterization of Monoclonal Antibody Broadly Recognizing Cry1 Toxins by Use of Designed Polypeptide as Hapten</atitle><jtitle>Analytical chemistry (Washington)</jtitle><addtitle>Anal. Chem</addtitle><date>2016-07-19</date><risdate>2016</risdate><volume>88</volume><issue>14</issue><spage>7023</spage><epage>7032</epage><pages>7023-7032</pages><issn>0003-2700</issn><eissn>1520-6882</eissn><coden>ANCHAM</coden><abstract>In this study, by use of synthesized polypeptides as haptens, a monoclonal antibody with broad recognition against seven major Cry1 toxins (Cry1Aa, Cry1Ab, Cry1Ac, Cry1B, Cry1C, Cry1E, and Cry1F) has been produced and characterized. First, by comparing the three-dimensional structures of seven Cry1 toxins, analyzing the conserved sequences, and considering the antigenicity and hydrophilicity, three polypeptides (T1, T2, and T3) have been chosen and coupled to keyhole limpet hemocyanin as immunogens for the generic monoclonal antibody (Mab) generation. Thereafter, a double antibody sandwich enzyme-linked immunosorbent assay method (DAS-ELISA) was developed for simultaneous determination of seven Cry1 toxins. The results revealed that the haptens T1, T2, and T3 had different effects in the production of antibodies. Among them, the obtained Mab (strain 2D3) generated by T2 can recognize seven Cry1 toxins simultaneously. Equilibrium dissociation constant (K D) values for seven Cry1 toxins with Mab 2D3 were 1.198 × 10–8 M for Cry1Aa, 2.197 × 10–8 M for Cry1Ab, 1.367 × 10–8 M for Cry1Ac, 2.092 × 10–8 M for Cry1B, 5.177 × 10–8 M for Cry1C, 4.016 × 10–8 M for Cry1E, and 3.497 × 10–8 M for Cry1F. For 2D3-based DAS-ELISA, the limits of detection (LOD) and limits of quantification (LOQ) can reach 15 and 30 ng·mL–1 for each Cry1 toxin, respectively. Our study is the first report of a broadly specific immunoassay for multidetermination of seven major Cry1 toxins, and it will provide a new idea and technical routes for development of multidetermination immunoassays.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>27341419</pmid><doi>10.1021/acs.analchem.6b00429</doi><tpages>10</tpages></addata></record> |
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subjects | Antibodies Comparative analysis Constants Immunoassay Joining Monoclonal antibodies Polypeptides Recognition Toxins |
title | Production and Characterization of Monoclonal Antibody Broadly Recognizing Cry1 Toxins by Use of Designed Polypeptide as Hapten |
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