501Y.V2 and 501Y.V3 variants of SARS-CoV-2 lose binding to bamlanivimab in vitro

The newly emerging variants of SARS-CoV-2 from South Africa (B.1.351/501Y.V2) and Brazil (P.1/501Y.V3) have led to a higher infection rate and reinfection of COVID-19 patients. We found that the mutations K417N, E484K, and N501Y within the receptor-binding domains (RBDs) of the virus could confer ~2...

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Bibliografiske detaljer
Main Authors: Haolin Liu, Pengcheng Wei, Qianqian Zhang, Zhongzhou Chen, Katja Aviszus, Walter Downing, Shelley Peterson, Lyndon Reynoso, Gregory P. Downey, Stephen K. Frankel, John Kappler, Philippa Marrack, Gongyi Zhang
Format: Artigo
Sprog:Inglês
Udgivet: Taylor & Francis Group 2021-01-01
Serier:mAbs
Fag:
SARS-COV-2
COVID-19
B.1.1.7/501Y.V1
B.1.351/501Y.V2
P.1/501Y.V3
ACE2
Online adgang:https://www.tandfonline.com/doi/10.1080/19420862.2021.1919285
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