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Human antibodies to SARS-CoV-2 with a recurring YYDRxG motif retain binding and neutralization to variants of concern including Omicron

Studying the antibody response to SARS-CoV-2 informs on how the human immune system can respond to antigenic variants as well as other SARS-related viruses. Here, we structurally identified a YYDRxG motif encoded by IGHD3-22 in CDR H3 that facilitates antibody targeting to a functionally conserved e...

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Autores principales: Liu, Hejun, Kaku, Chengzi I., Song, Ge, Yuan, Meng, Andrabi, Raiees, Burton, Dennis R., Walker, Laura M., Wilson, Ian A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9336126/
https://www.ncbi.nlm.nih.gov/pubmed/35906394
http://dx.doi.org/10.1038/s42003-022-03700-6
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author Liu, Hejun
Kaku, Chengzi I.
Song, Ge
Yuan, Meng
Andrabi, Raiees
Burton, Dennis R.
Walker, Laura M.
Wilson, Ian A.
author_facet Liu, Hejun
Kaku, Chengzi I.
Song, Ge
Yuan, Meng
Andrabi, Raiees
Burton, Dennis R.
Walker, Laura M.
Wilson, Ian A.
author_sort Liu, Hejun
collection PubMed
description Studying the antibody response to SARS-CoV-2 informs on how the human immune system can respond to antigenic variants as well as other SARS-related viruses. Here, we structurally identified a YYDRxG motif encoded by IGHD3-22 in CDR H3 that facilitates antibody targeting to a functionally conserved epitope on the SARS-CoV-2 receptor binding domain. A computational search for a YYDRxG pattern in publicly available sequences uncovered 100 such antibodies, many of which can neutralize SARS-CoV-2 variants and SARS-CoV. Thus, the YYDRxG motif represents a common convergent solution for the human humoral immune system to target sarbecoviruses including the Omicron variant. These findings suggest an epitope-targeting strategy to identify potent and broadly neutralizing antibodies for design of pan-sarbecovirus vaccines and antibody therapeutics.
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spelling pubmed-93361262022-07-29 Human antibodies to SARS-CoV-2 with a recurring YYDRxG motif retain binding and neutralization to variants of concern including Omicron Liu, Hejun Kaku, Chengzi I. Song, Ge Yuan, Meng Andrabi, Raiees Burton, Dennis R. Walker, Laura M. Wilson, Ian A. Commun Biol Article Studying the antibody response to SARS-CoV-2 informs on how the human immune system can respond to antigenic variants as well as other SARS-related viruses. Here, we structurally identified a YYDRxG motif encoded by IGHD3-22 in CDR H3 that facilitates antibody targeting to a functionally conserved epitope on the SARS-CoV-2 receptor binding domain. A computational search for a YYDRxG pattern in publicly available sequences uncovered 100 such antibodies, many of which can neutralize SARS-CoV-2 variants and SARS-CoV. Thus, the YYDRxG motif represents a common convergent solution for the human humoral immune system to target sarbecoviruses including the Omicron variant. These findings suggest an epitope-targeting strategy to identify potent and broadly neutralizing antibodies for design of pan-sarbecovirus vaccines and antibody therapeutics. Nature Publishing Group UK 2022-07-29 /pmc/articles/PMC9336126/ /pubmed/35906394 http://dx.doi.org/10.1038/s42003-022-03700-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Liu, Hejun
Kaku, Chengzi I.
Song, Ge
Yuan, Meng
Andrabi, Raiees
Burton, Dennis R.
Walker, Laura M.
Wilson, Ian A.
Human antibodies to SARS-CoV-2 with a recurring YYDRxG motif retain binding and neutralization to variants of concern including Omicron
title Human antibodies to SARS-CoV-2 with a recurring YYDRxG motif retain binding and neutralization to variants of concern including Omicron
title_full Human antibodies to SARS-CoV-2 with a recurring YYDRxG motif retain binding and neutralization to variants of concern including Omicron
title_fullStr Human antibodies to SARS-CoV-2 with a recurring YYDRxG motif retain binding and neutralization to variants of concern including Omicron
title_full_unstemmed Human antibodies to SARS-CoV-2 with a recurring YYDRxG motif retain binding and neutralization to variants of concern including Omicron
title_short Human antibodies to SARS-CoV-2 with a recurring YYDRxG motif retain binding and neutralization to variants of concern including Omicron
title_sort human antibodies to sars-cov-2 with a recurring yydrxg motif retain binding and neutralization to variants of concern including omicron
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9336126/
https://www.ncbi.nlm.nih.gov/pubmed/35906394
http://dx.doi.org/10.1038/s42003-022-03700-6
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