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Potent neutralization of SARS-CoV-2 variants of concern by an antibody with an uncommon genetic signature and structural mode of spike recognition

The emergence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) lineages that are more transmissible and resistant to currently approved antibody therapies poses a considerable challenge to the clinical treatment of coronavirus disease (COVID-19). Therefore, the need for ongoing discov...

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Autores principales: Kramer, Kevin J., Johnson, Nicole V., Shiakolas, Andrea R., Suryadevara, Naveenchandra, Periasamy, Sivakumar, Raju, Nagarajan, Williams, Jazmean K., Wrapp, Daniel, Zost, Seth J., Walker, Lauren M., Wall, Steven C., Holt, Clinton M., Hsieh, Ching-Lin, Sutton, Rachel E., Paulo, Ariana, Nargi, Rachel S., Davidson, Edgar, Doranz, Benjamin J., Crowe, James E., Bukreyev, Alexander, Carnahan, Robert H., McLellan, Jason S., Georgiev, Ivelin S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Author(s). 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8443366/
https://www.ncbi.nlm.nih.gov/pubmed/34592170
http://dx.doi.org/10.1016/j.celrep.2021.109784
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author Kramer, Kevin J.
Johnson, Nicole V.
Shiakolas, Andrea R.
Suryadevara, Naveenchandra
Periasamy, Sivakumar
Raju, Nagarajan
Williams, Jazmean K.
Wrapp, Daniel
Zost, Seth J.
Walker, Lauren M.
Wall, Steven C.
Holt, Clinton M.
Hsieh, Ching-Lin
Sutton, Rachel E.
Paulo, Ariana
Nargi, Rachel S.
Davidson, Edgar
Doranz, Benjamin J.
Crowe, James E.
Bukreyev, Alexander
Carnahan, Robert H.
McLellan, Jason S.
Georgiev, Ivelin S.
author_facet Kramer, Kevin J.
Johnson, Nicole V.
Shiakolas, Andrea R.
Suryadevara, Naveenchandra
Periasamy, Sivakumar
Raju, Nagarajan
Williams, Jazmean K.
Wrapp, Daniel
Zost, Seth J.
Walker, Lauren M.
Wall, Steven C.
Holt, Clinton M.
Hsieh, Ching-Lin
Sutton, Rachel E.
Paulo, Ariana
Nargi, Rachel S.
Davidson, Edgar
Doranz, Benjamin J.
Crowe, James E.
Bukreyev, Alexander
Carnahan, Robert H.
McLellan, Jason S.
Georgiev, Ivelin S.
author_sort Kramer, Kevin J.
collection PubMed
description The emergence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) lineages that are more transmissible and resistant to currently approved antibody therapies poses a considerable challenge to the clinical treatment of coronavirus disease (COVID-19). Therefore, the need for ongoing discovery efforts to identify broadly reactive monoclonal antibodies to SARS-CoV-2 is of utmost importance. Here, we report a panel of SARS-CoV-2 antibodies isolated using the linking B cell receptor to antigen specificity through sequencing (LIBRA-seq) technology from an individual who recovered from COVID-19. Of these antibodies, 54042-4 shows potent neutralization against authentic SARS-CoV-2 viruses, including variants of concern (VOCs). A cryoelectron microscopy (cryo-EM) structure of 54042-4 in complex with the SARS-CoV-2 spike reveals an epitope composed of residues that are highly conserved in currently circulating SARS-CoV-2 lineages. Further, 54042-4 possesses uncommon genetic and structural characteristics that distinguish it from other potently neutralizing SARS-CoV-2 antibodies. Together, these findings provide motivation for the development of 54042-4 as a lead candidate to counteract current and future SARS-CoV-2 VOCs.
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spelling pubmed-84433662021-09-16 Potent neutralization of SARS-CoV-2 variants of concern by an antibody with an uncommon genetic signature and structural mode of spike recognition Kramer, Kevin J. Johnson, Nicole V. Shiakolas, Andrea R. Suryadevara, Naveenchandra Periasamy, Sivakumar Raju, Nagarajan Williams, Jazmean K. Wrapp, Daniel Zost, Seth J. Walker, Lauren M. Wall, Steven C. Holt, Clinton M. Hsieh, Ching-Lin Sutton, Rachel E. Paulo, Ariana Nargi, Rachel S. Davidson, Edgar Doranz, Benjamin J. Crowe, James E. Bukreyev, Alexander Carnahan, Robert H. McLellan, Jason S. Georgiev, Ivelin S. Cell Rep Article The emergence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) lineages that are more transmissible and resistant to currently approved antibody therapies poses a considerable challenge to the clinical treatment of coronavirus disease (COVID-19). Therefore, the need for ongoing discovery efforts to identify broadly reactive monoclonal antibodies to SARS-CoV-2 is of utmost importance. Here, we report a panel of SARS-CoV-2 antibodies isolated using the linking B cell receptor to antigen specificity through sequencing (LIBRA-seq) technology from an individual who recovered from COVID-19. Of these antibodies, 54042-4 shows potent neutralization against authentic SARS-CoV-2 viruses, including variants of concern (VOCs). A cryoelectron microscopy (cryo-EM) structure of 54042-4 in complex with the SARS-CoV-2 spike reveals an epitope composed of residues that are highly conserved in currently circulating SARS-CoV-2 lineages. Further, 54042-4 possesses uncommon genetic and structural characteristics that distinguish it from other potently neutralizing SARS-CoV-2 antibodies. Together, these findings provide motivation for the development of 54042-4 as a lead candidate to counteract current and future SARS-CoV-2 VOCs. The Author(s). 2021-10-05 2021-09-16 /pmc/articles/PMC8443366/ /pubmed/34592170 http://dx.doi.org/10.1016/j.celrep.2021.109784 Text en © 2021 The Author(s) Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Kramer, Kevin J.
Johnson, Nicole V.
Shiakolas, Andrea R.
Suryadevara, Naveenchandra
Periasamy, Sivakumar
Raju, Nagarajan
Williams, Jazmean K.
Wrapp, Daniel
Zost, Seth J.
Walker, Lauren M.
Wall, Steven C.
Holt, Clinton M.
Hsieh, Ching-Lin
Sutton, Rachel E.
Paulo, Ariana
Nargi, Rachel S.
Davidson, Edgar
Doranz, Benjamin J.
Crowe, James E.
Bukreyev, Alexander
Carnahan, Robert H.
McLellan, Jason S.
Georgiev, Ivelin S.
Potent neutralization of SARS-CoV-2 variants of concern by an antibody with an uncommon genetic signature and structural mode of spike recognition
title Potent neutralization of SARS-CoV-2 variants of concern by an antibody with an uncommon genetic signature and structural mode of spike recognition
title_full Potent neutralization of SARS-CoV-2 variants of concern by an antibody with an uncommon genetic signature and structural mode of spike recognition
title_fullStr Potent neutralization of SARS-CoV-2 variants of concern by an antibody with an uncommon genetic signature and structural mode of spike recognition
title_full_unstemmed Potent neutralization of SARS-CoV-2 variants of concern by an antibody with an uncommon genetic signature and structural mode of spike recognition
title_short Potent neutralization of SARS-CoV-2 variants of concern by an antibody with an uncommon genetic signature and structural mode of spike recognition
title_sort potent neutralization of sars-cov-2 variants of concern by an antibody with an uncommon genetic signature and structural mode of spike recognition
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8443366/
https://www.ncbi.nlm.nih.gov/pubmed/34592170
http://dx.doi.org/10.1016/j.celrep.2021.109784
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