Structural characteristics and biological functions of the HIV-1 gp120 V3 region
Recent studies demonstrate that the V3 loop of HIV-1 gp120 plays an important role in the attachment of HIV-1 to the target cells. Several amino acids in this domain are involved in the interaction of gp120 with the co-receptors. The V3 loop elicits one of the earliest antiviral antibody responses i...
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Veröffentlicht in: | Progress in natural science 2002-11, Vol.12 (11), p.808-812 |
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description | Recent studies demonstrate that the V3 loop of HIV-1 gp120 plays an important role in the attachment of HIV-1 to the target cells. Several amino acids in this domain are involved in the interaction of gp120 with the co-receptors. The V3 loop elicits one of the earliest antiviral antibody responses in HIV-1 infection and has been identified as the principal neutralizing determinant (PND). A subset of antibodies to V3 loop show a broad range of neutralizing activity. Unfortunately, this loop undergoes broad mutation and is one of the hypervariable regions. Mutations of some amino acids in this PND could affect syncytium formation, virus infectivity and neutralization. Knowing the structural characteristics and biological functions of the V3 region could help us to understand mechanism of HIV infection and to develop new strategy against HIV-1. In this review, the structural characteristics, variation and biological functions of the V3 loop as well as immunological responses to the V3 loop are discussed. |
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Several amino acids in this domain are involved in the interaction of gp120 with the co-receptors. The V3 loop elicits one of the earliest antiviral antibody responses in HIV-1 infection and has been identified as the principal neutralizing determinant (PND). A subset of antibodies to V3 loop show a broad range of neutralizing activity. Unfortunately, this loop undergoes broad mutation and is one of the hypervariable regions. Mutations of some amino acids in this PND could affect syncytium formation, virus infectivity and neutralization. Knowing the structural characteristics and biological functions of the V3 region could help us to understand mechanism of HIV infection and to develop new strategy against HIV-1. In this review, the structural characteristics, variation and biological functions of the V3 loop as well as immunological responses to the V3 loop are discussed.</description><identifier>ISSN: 1002-0071</identifier><language>eng</language><publisher>Protein Science Laboratory of the Ministry of Education, Beijing 100084, China%Lindsley F.Kimball Research Institute,New York Blood Center,USA</publisher><subject>biological ; epitope ; function ; HIV-1 ; loop ; neutralizing ; structure</subject><ispartof>Progress in natural science, 2002-11, Vol.12 (11), p.808-812</ispartof><rights>Copyright © Wanfang Data Co. Ltd. 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The V3 loop elicits one of the earliest antiviral antibody responses in HIV-1 infection and has been identified as the principal neutralizing determinant (PND). A subset of antibodies to V3 loop show a broad range of neutralizing activity. Unfortunately, this loop undergoes broad mutation and is one of the hypervariable regions. Mutations of some amino acids in this PND could affect syncytium formation, virus infectivity and neutralization. Knowing the structural characteristics and biological functions of the V3 region could help us to understand mechanism of HIV infection and to develop new strategy against HIV-1. In this review, the structural characteristics, variation and biological functions of the V3 loop as well as immunological responses to the V3 loop are discussed.</description><subject>biological</subject><subject>epitope</subject><subject>function</subject><subject>HIV-1</subject><subject>loop</subject><subject>neutralizing</subject><subject>structure</subject><issn>1002-0071</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNotj1FLwzAUhfOg4Jz-hzz44kMhN7FN-ihD3WCgoO61pLdJm62kmqQo-_VmzKdz4fu4h3NBFsAYLxiTcEWuY9yz01nJBXl7T2HGNAc9Uhx00JhMcDE5jFT7jrZuGqfeYcZ29pjc5COdLE2DoevNrgDafwFndCdoMH2mN-TS6jGa2_9cks_np4_Vuti-vmxWj9sCOahU1KgkgC5BdKplHLWVAhBZBw-1Fl0tO-xKYxUTEqSplUIGMjPQ3MgWK7Ek9-e_P9pb7ftmP83B58bmGA6_-2NjeJ4Mp93ZvTu7OEy-_3bZbjUerBtNkwUQquSVFH_qjlbt</recordid><startdate>20021101</startdate><enddate>20021101</enddate><creator>TIAN Haijun LAN Canhui JIANG Shibo CHEN Yinghua</creator><general>Protein Science Laboratory of the Ministry of Education, Beijing 100084, China%Lindsley F.Kimball Research Institute,New York Blood Center,USA</general><general>Laboratory of Immunology, Department of Biological Science and Biotechnology, Tsinghua University</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W91</scope><scope>~WA</scope><scope>2B.</scope><scope>4A8</scope><scope>92I</scope><scope>93N</scope><scope>PSX</scope><scope>TCJ</scope></search><sort><creationdate>20021101</creationdate><title>Structural characteristics and biological functions of the HIV-1 gp120 V3 region</title><author>TIAN Haijun LAN Canhui JIANG Shibo CHEN Yinghua</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c218t-9c8711a513d8b02caf731cc0d149a3d97dcd5ef803717e988c0171491a2e7bc63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>biological</topic><topic>epitope</topic><topic>function</topic><topic>HIV-1</topic><topic>loop</topic><topic>neutralizing</topic><topic>structure</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>TIAN Haijun LAN Canhui JIANG Shibo CHEN Yinghua</creatorcontrib><collection>中文科技期刊数据库</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>中文科技期刊数据库-7.0平台</collection><collection>中文科技期刊数据库-医药卫生</collection><collection>中文科技期刊数据库- 镜像站点</collection><collection>Wanfang Data Journals - Hong Kong</collection><collection>WANFANG Data Centre</collection><collection>Wanfang Data Journals</collection><collection>万方数据期刊 - 香港版</collection><collection>China Online Journals (COJ)</collection><collection>China Online Journals (COJ)</collection><jtitle>Progress in natural science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>TIAN Haijun LAN Canhui JIANG Shibo CHEN Yinghua</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Structural characteristics and biological functions of the HIV-1 gp120 V3 region</atitle><jtitle>Progress in natural science</jtitle><addtitle>Progress in Natural Science</addtitle><date>2002-11-01</date><risdate>2002</risdate><volume>12</volume><issue>11</issue><spage>808</spage><epage>812</epage><pages>808-812</pages><issn>1002-0071</issn><abstract>Recent studies demonstrate that the V3 loop of HIV-1 gp120 plays an important role in the attachment of HIV-1 to the target cells. Several amino acids in this domain are involved in the interaction of gp120 with the co-receptors. The V3 loop elicits one of the earliest antiviral antibody responses in HIV-1 infection and has been identified as the principal neutralizing determinant (PND). A subset of antibodies to V3 loop show a broad range of neutralizing activity. Unfortunately, this loop undergoes broad mutation and is one of the hypervariable regions. Mutations of some amino acids in this PND could affect syncytium formation, virus infectivity and neutralization. Knowing the structural characteristics and biological functions of the V3 region could help us to understand mechanism of HIV infection and to develop new strategy against HIV-1. In this review, the structural characteristics, variation and biological functions of the V3 loop as well as immunological responses to the V3 loop are discussed.</abstract><pub>Protein Science Laboratory of the Ministry of Education, Beijing 100084, China%Lindsley F.Kimball Research Institute,New York Blood Center,USA</pub><tpages>5</tpages></addata></record> |
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subjects | biological epitope function HIV-1 loop neutralizing structure |
title | Structural characteristics and biological functions of the HIV-1 gp120 V3 region |
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