6bzy

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<StructureSection load='6bzy' size='340' side='right' caption='[[6bzy]], [[Resolution|resolution]] 1.60&Aring;' scene=''>
<StructureSection load='6bzy' size='340' side='right' caption='[[6bzy]], [[Resolution|resolution]] 1.60&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
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<table><tr><td colspan='2'>[[6bzy]] is a 3 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6BZY OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6BZY FirstGlance]. <br>
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<table><tr><td colspan='2'>[[6bzy]] is a 3 chain structure with sequence from [http://en.wikipedia.org/wiki/9hepc 9hepc] and [http://en.wikipedia.org/wiki/Lk3_transgenic_mice Lk3 transgenic mice]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6BZY OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6BZY FirstGlance]. <br>
</td></tr><tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6bzy FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6bzy OCA], [http://pdbe.org/6bzy PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6bzy RCSB], [http://www.ebi.ac.uk/pdbsum/6bzy PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6bzy ProSAT]</span></td></tr>
</td></tr><tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6bzy FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6bzy OCA], [http://pdbe.org/6bzy PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6bzy RCSB], [http://www.ebi.ac.uk/pdbsum/6bzy PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6bzy ProSAT]</span></td></tr>
</table>
</table>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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Elicitation of broadly neutralizing antibodies (bnAbs) is a leading strategy in rational vaccine design against antigenically diverse pathogens. Here, we studied a panel of monoclonal antibodies (mAbs) from mice immunized with the hepatitis C virus (HCV) envelope glycoproteins E1E2. Six of the mAbs recognize the conserved E2 antigenic site 412-423 (AS412) and cross-neutralize diverse HCV genotypes. Immunogenetic and structural analysis revealed that the antibodies originated from two different germline (GL) precursors and bind AS412 in a beta-hairpin conformation. Intriguingly, the anti-HCV activity of one antibody lineage is associated with maturation of the light chain (LC), whereas the other lineage is dependent on heavy-chain (HC) maturation. Crystal structures of GL precursors of the LC-dependent lineage in complex with AS412 offer critical insights into the maturation process of bnAbs to HCV, providing a scientific foundation for utilizing the mouse model to study AS412-targeting vaccine candidates.
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Immunogenetic and structural analysis of a class of HCV broadly neutralizing antibodies and their precursors.,Aleman F, Tzarum N, Kong L, Nagy K, Zhu J, Wilson IA, Law M Proc Natl Acad Sci U S A. 2018 Jun 28. pii: 1802378115. doi:, 10.1073/pnas.1802378115. PMID:29954862<ref>PMID:29954862</ref>
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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</div>
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<div class="pdbe-citations 6bzy" style="background-color:#fffaf0;"></div>
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== References ==
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<references/>
__TOC__
__TOC__
</StructureSection>
</StructureSection>
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[[Category: Lk3 transgenic mice]]
[[Category: Alemn, F]]
[[Category: Alemn, F]]
[[Category: Law, M]]
[[Category: Law, M]]

Revision as of 06:12, 11 July 2018

Structure of the Hepatitis C virus envelope glycoprotein E2 antigenic region 412-423 bound to the 22D11 broadly neutralizing antibody

6bzy, resolution 1.60Å

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