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Impact of the N501Y substitution of SARS-CoV-2 Spike on neutralizing monoclonal antibodies targeting diverse epitopes

The emergence and rapid spread of the B.1.1.7 lineage (VOC-202012/01) SARS-CoV-2 variant has aroused global concern. The N501Y substitution is the only mutation in the interface between the RBD of B.1.1.7 and ACE2, raising concerns that its recognition by neutralizing antibodies may be affected. Her...

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Autores principales: Cheng, Lin, Song, Shuo, Zhou, Bing, Ge, Xiangyang, Yu, Jiazhen, Zhang, Mingxia, Ju, Bin, Zhang, Zheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8081001/
https://www.ncbi.nlm.nih.gov/pubmed/33910569
http://dx.doi.org/10.1186/s12985-021-01554-8
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author Cheng, Lin
Song, Shuo
Zhou, Bing
Ge, Xiangyang
Yu, Jiazhen
Zhang, Mingxia
Ju, Bin
Zhang, Zheng
author_facet Cheng, Lin
Song, Shuo
Zhou, Bing
Ge, Xiangyang
Yu, Jiazhen
Zhang, Mingxia
Ju, Bin
Zhang, Zheng
author_sort Cheng, Lin
collection PubMed
description The emergence and rapid spread of the B.1.1.7 lineage (VOC-202012/01) SARS-CoV-2 variant has aroused global concern. The N501Y substitution is the only mutation in the interface between the RBD of B.1.1.7 and ACE2, raising concerns that its recognition by neutralizing antibodies may be affected. Here, we assessed the neutralizing activity and binding affinity of a panel of 12 monoclonal antibodies against the wild type and N501Y mutant SARS-CoV-2 pseudovirus and RBD protein, respectively. We found that the neutralization activity and binding affinity of most detected antibodies (10 out of 12) were unaffected, although the N501Y substitution decreased the neutralizing and binding activities of CB6 and increased that of BD-23. These findings could be of value in the development of therapeutic antibodies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12985-021-01554-8.
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spelling pubmed-80810012021-04-29 Impact of the N501Y substitution of SARS-CoV-2 Spike on neutralizing monoclonal antibodies targeting diverse epitopes Cheng, Lin Song, Shuo Zhou, Bing Ge, Xiangyang Yu, Jiazhen Zhang, Mingxia Ju, Bin Zhang, Zheng Virol J Short Report The emergence and rapid spread of the B.1.1.7 lineage (VOC-202012/01) SARS-CoV-2 variant has aroused global concern. The N501Y substitution is the only mutation in the interface between the RBD of B.1.1.7 and ACE2, raising concerns that its recognition by neutralizing antibodies may be affected. Here, we assessed the neutralizing activity and binding affinity of a panel of 12 monoclonal antibodies against the wild type and N501Y mutant SARS-CoV-2 pseudovirus and RBD protein, respectively. We found that the neutralization activity and binding affinity of most detected antibodies (10 out of 12) were unaffected, although the N501Y substitution decreased the neutralizing and binding activities of CB6 and increased that of BD-23. These findings could be of value in the development of therapeutic antibodies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12985-021-01554-8. BioMed Central 2021-04-28 /pmc/articles/PMC8081001/ /pubmed/33910569 http://dx.doi.org/10.1186/s12985-021-01554-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Short Report
Cheng, Lin
Song, Shuo
Zhou, Bing
Ge, Xiangyang
Yu, Jiazhen
Zhang, Mingxia
Ju, Bin
Zhang, Zheng
Impact of the N501Y substitution of SARS-CoV-2 Spike on neutralizing monoclonal antibodies targeting diverse epitopes
title Impact of the N501Y substitution of SARS-CoV-2 Spike on neutralizing monoclonal antibodies targeting diverse epitopes
title_full Impact of the N501Y substitution of SARS-CoV-2 Spike on neutralizing monoclonal antibodies targeting diverse epitopes
title_fullStr Impact of the N501Y substitution of SARS-CoV-2 Spike on neutralizing monoclonal antibodies targeting diverse epitopes
title_full_unstemmed Impact of the N501Y substitution of SARS-CoV-2 Spike on neutralizing monoclonal antibodies targeting diverse epitopes
title_short Impact of the N501Y substitution of SARS-CoV-2 Spike on neutralizing monoclonal antibodies targeting diverse epitopes
title_sort impact of the n501y substitution of sars-cov-2 spike on neutralizing monoclonal antibodies targeting diverse epitopes
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8081001/
https://www.ncbi.nlm.nih.gov/pubmed/33910569
http://dx.doi.org/10.1186/s12985-021-01554-8
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