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A highly conserved cryptic epitope in the receptor-binding domains of SARS-CoV-2 and SARS-CoV

Identifieur interne : 000A34 ( Main/Exploration ); précédent : 000A33; suivant : 000A35

A highly conserved cryptic epitope in the receptor-binding domains of SARS-CoV-2 and SARS-CoV

Auteurs : Meng Yuan [États-Unis] ; Nicholas C. Wu [États-Unis] ; Xueyong Zhu [États-Unis] ; Chang-Chun D. Lee [États-Unis] ; Ray T. Y. So [République populaire de Chine] ; Huibin Lv [République populaire de Chine] ; Chris K. P. Mok [République populaire de Chine] ; Ian A. Wilson [États-Unis]

Source :

RBID : PMC:7164391

Abstract

The outbreak of COVID-19 caused by SARS-CoV-2 virus has now become a pandemic, but there is currently very little understanding of the antigenicity of the virus. We therefore determined the crystal structure of CR3022, a neutralizing antibody previously isolated from a convalescent SARS patient, in complex with the receptor-binding domain (RBD) of the SARS-CoV-2 spike (S) protein to 3.1 Å. CR3022 targets a highly conserved epitope, distal from the receptor-binding site, that enables cross-reactive binding between SARS-CoV-2 and SARS-CoV. Structural modeling further demonstrates that the binding epitope can only be accessed by CR3022 when at least two RBD on the trimeric S protein are in the “up” conformation and slightly rotated. Overall, this study provides molecular insights into antibody recognition of SARS-CoV-2.


Url:
DOI: 10.1126/science.abb7269
PubMed: 32245784
PubMed Central: 7164391


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<p>The outbreak of COVID-19 caused by SARS-CoV-2 virus has now become a pandemic, but there is currently very little understanding of the antigenicity of the virus. We therefore determined the crystal structure of CR3022, a neutralizing antibody previously isolated from a convalescent SARS patient, in complex with the receptor-binding domain (RBD) of the SARS-CoV-2 spike (S) protein to 3.1 Å. CR3022 targets a highly conserved epitope, distal from the receptor-binding site, that enables cross-reactive binding between SARS-CoV-2 and SARS-CoV. Structural modeling further demonstrates that the binding epitope can only be accessed by CR3022 when at least two RBD on the trimeric S protein are in the “up” conformation and slightly rotated. Overall, this study provides molecular insights into antibody recognition of SARS-CoV-2.</p>
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<name sortKey="Read, R J" uniqKey="Read R">R. J. Read</name>
</author>
<author>
<name sortKey="Richardson, D C" uniqKey="Richardson D">D. C. Richardson</name>
</author>
<author>
<name sortKey="Richardson, J S" uniqKey="Richardson J">J. S. Richardson</name>
</author>
<author>
<name sortKey="Terwilliger, T C" uniqKey="Terwilliger T">T. C. Terwilliger</name>
</author>
<author>
<name sortKey="Zwart, P H" uniqKey="Zwart P">P. H. Zwart</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Wu, N C" uniqKey="Wu N">N. C. Wu</name>
</author>
<author>
<name sortKey="Grande, G" uniqKey="Grande G">G. Grande</name>
</author>
<author>
<name sortKey="Turner, H L" uniqKey="Turner H">H. L. Turner</name>
</author>
<author>
<name sortKey="Ward, A B" uniqKey="Ward A">A. B. Ward</name>
</author>
<author>
<name sortKey="Xie, J" uniqKey="Xie J">J. Xie</name>
</author>
<author>
<name sortKey="Lerner, R A" uniqKey="Lerner R">R. A. Lerner</name>
</author>
<author>
<name sortKey="Wilson, I A" uniqKey="Wilson I">I. A. Wilson</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Song, W" uniqKey="Song W">W. Song</name>
</author>
<author>
<name sortKey="Gui, M" uniqKey="Gui M">M. Gui</name>
</author>
<author>
<name sortKey="Wang, X" uniqKey="Wang X">X. Wang</name>
</author>
<author>
<name sortKey="Xiang, Y" uniqKey="Xiang Y">Y. Xiang</name>
</author>
</analytic>
</biblStruct>
</listBibl>
</div1>
</back>
</TEI>
<affiliations>
<list>
<country>
<li>République populaire de Chine</li>
<li>États-Unis</li>
</country>
<region>
<li>Californie</li>
</region>
</list>
<tree>
<country name="États-Unis">
<region name="Californie">
<name sortKey="Yuan, Meng" sort="Yuan, Meng" uniqKey="Yuan M" first="Meng" last="Yuan">Meng Yuan</name>
</region>
<name sortKey="Lee, Chang Chun D" sort="Lee, Chang Chun D" uniqKey="Lee C" first="Chang-Chun D." last="Lee">Chang-Chun D. Lee</name>
<name sortKey="Wilson, Ian A" sort="Wilson, Ian A" uniqKey="Wilson I" first="Ian A." last="Wilson">Ian A. Wilson</name>
<name sortKey="Wilson, Ian A" sort="Wilson, Ian A" uniqKey="Wilson I" first="Ian A." last="Wilson">Ian A. Wilson</name>
<name sortKey="Wu, Nicholas C" sort="Wu, Nicholas C" uniqKey="Wu N" first="Nicholas C." last="Wu">Nicholas C. Wu</name>
<name sortKey="Zhu, Xueyong" sort="Zhu, Xueyong" uniqKey="Zhu X" first="Xueyong" last="Zhu">Xueyong Zhu</name>
</country>
<country name="République populaire de Chine">
<noRegion>
<name sortKey="So, Ray T Y" sort="So, Ray T Y" uniqKey="So R" first="Ray T. Y." last="So">Ray T. Y. So</name>
</noRegion>
<name sortKey="Lv, Huibin" sort="Lv, Huibin" uniqKey="Lv H" first="Huibin" last="Lv">Huibin Lv</name>
<name sortKey="Mok, Chris K P" sort="Mok, Chris K P" uniqKey="Mok C" first="Chris K. P." last="Mok">Chris K. P. Mok</name>
</country>
</tree>
</affiliations>
</record>

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