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6ws6
From Proteopedia
(Difference between revisions)
(New page: '''Unreleased structure''' The entry 6ws6 is ON HOLD Authors: Description: Category: Unreleased Structures) |
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| - | '''Unreleased structure''' | ||
| - | The entry | + | ==Structural and functional analysis of a potent sarbecovirus neutralizing antibody== |
| + | <StructureSection load='6ws6' size='340' side='right'caption='[[6ws6]], [[Resolution|resolution]] 3.30Å' scene=''> | ||
| + | == Structural highlights == | ||
| + | <table><tr><td colspan='2'>[[6ws6]] is a 6 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6WS6 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6WS6 FirstGlance]. <br> | ||
| + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 3.3Å</td></tr> | ||
| + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=JEF:O-(O-(2-AMINOPROPYL)-O-(2-METHOXYETHYL)POLYPROPYLENE+GLYCOL+500)'>JEF</scene></td></tr> | ||
| + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=6ws6 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6ws6 OCA], [https://pdbe.org/6ws6 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6ws6 RCSB], [https://www.ebi.ac.uk/pdbsum/6ws6 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6ws6 ProSAT]</span></td></tr> | ||
| + | </table> | ||
| + | <div style="background-color:#fffaf0;"> | ||
| + | == Publication Abstract from PubMed == | ||
| + | Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a newly emerged coronavirus that is responsible for the current pandemic of coronavirus disease 2019 (COVID-19), which has resulted in more than 3.7 million infections and 260,000 deaths as of 6 May 2020(1,2). Vaccine and therapeutic discovery efforts are paramount to curb the pandemic spread of this zoonotic virus. The SARS-CoV-2 spike (S) glycoprotein promotes entry into host cells and is the main target of neutralizing antibodies. Here we describe several monoclonal antibodies that target the S glycoprotein of SARS-CoV-2, which we identified from memory B cells of an individual who was infected with severe acute respiratory syndrome coronavirus (SARS-CoV) in 2003. One antibody (named S309) potently neutralizes SARS-CoV-2 and SARS-CoV pseudoviruses as well as authentic SARS-CoV-2, by engaging the receptor-binding domain of the S glycoprotein. Using cryo-electron microscopy and binding assays, we show that S309 recognizes an epitope containing a glycan that is conserved within the Sarbecovirus subgenus, without competing with receptor attachment. Antibody cocktails that include S309 in combination with other antibodies that we identified further enhanced SARS-CoV-2 neutralization, and may limit the emergence of neutralization-escape mutants. These results pave the way for using S309 and antibody cocktails containing S309 for prophylaxis in individuals at a high risk of exposure or as a post-exposure therapy to limit or treat severe disease. | ||
| - | + | Cross-neutralization of SARS-CoV-2 by a human monoclonal SARS-CoV antibody.,Pinto D, Park YJ, Beltramello M, Walls AC, Tortorici MA, Bianchi S, Jaconi S, Culap K, Zatta F, De Marco A, Peter A, Guarino B, Spreafico R, Cameroni E, Case JB, Chen RE, Havenar-Daughton C, Snell G, Telenti A, Virgin HW, Lanzavecchia A, Diamond MS, Fink K, Veesler D, Corti D Nature. 2020 Jul;583(7815):290-295. doi: 10.1038/s41586-020-2349-y. Epub 2020 May, 18. PMID:32422645<ref>PMID:32422645</ref> | |
| - | + | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | |
| - | [[Category: | + | </div> |
| + | <div class="pdbe-citations 6ws6" style="background-color:#fffaf0;"></div> | ||
| + | |||
| + | ==See Also== | ||
| + | *[[Antibody 3D structures|Antibody 3D structures]] | ||
| + | == References == | ||
| + | <references/> | ||
| + | __TOC__ | ||
| + | </StructureSection> | ||
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Large Structures]] | ||
| + | [[Category: Beltramello M]] | ||
| + | [[Category: Bianchi S]] | ||
| + | [[Category: Cameroni E]] | ||
| + | [[Category: Case JB]] | ||
| + | [[Category: Chen RE]] | ||
| + | [[Category: Corti D]] | ||
| + | [[Category: Culap K]] | ||
| + | [[Category: Diamond MS]] | ||
| + | [[Category: Fink K]] | ||
| + | [[Category: Guarino B]] | ||
| + | [[Category: Havenar-Daughton C]] | ||
| + | [[Category: Jaconi S]] | ||
| + | [[Category: Lanzavecchia A]] | ||
| + | [[Category: Marco AD]] | ||
| + | [[Category: Park YJ]] | ||
| + | [[Category: Peter A]] | ||
| + | [[Category: Pinto D]] | ||
| + | [[Category: Snell G]] | ||
| + | [[Category: Spreafico R]] | ||
| + | [[Category: Telenti A]] | ||
| + | [[Category: Tortorici MA]] | ||
| + | [[Category: Veesler D]] | ||
| + | [[Category: Virgin HW]] | ||
| + | [[Category: Walls AC]] | ||
| + | [[Category: Zatta F]] | ||
Current revision
Structural and functional analysis of a potent sarbecovirus neutralizing antibody
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Categories: Homo sapiens | Large Structures | Beltramello M | Bianchi S | Cameroni E | Case JB | Chen RE | Corti D | Culap K | Diamond MS | Fink K | Guarino B | Havenar-Daughton C | Jaconi S | Lanzavecchia A | Marco AD | Park YJ | Peter A | Pinto D | Snell G | Spreafico R | Telenti A | Tortorici MA | Veesler D | Virgin HW | Walls AC | Zatta F
