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Identification of SARS-CoV-2 S RBD escape mutants using yeast screening and deep mutational scanning

Here, we describe a protocol to identify escape mutants on the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike (S) receptor-binding domain (RBD) using a yeast screen combined with deep mutational scanning. Over 90% of all potential single S RBD escape mutants can be identified for...

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Autores principales: Haas, Cyrus M., Francino-Urdaniz, Irene M., Steiner, Paul J., Whitehead, Timothy A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8455247/
https://www.ncbi.nlm.nih.gov/pubmed/34568839
http://dx.doi.org/10.1016/j.xpro.2021.100869
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author Haas, Cyrus M.
Francino-Urdaniz, Irene M.
Steiner, Paul J.
Whitehead, Timothy A.
author_facet Haas, Cyrus M.
Francino-Urdaniz, Irene M.
Steiner, Paul J.
Whitehead, Timothy A.
author_sort Haas, Cyrus M.
collection PubMed
description Here, we describe a protocol to identify escape mutants on the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike (S) receptor-binding domain (RBD) using a yeast screen combined with deep mutational scanning. Over 90% of all potential single S RBD escape mutants can be identified for monoclonal antibodies that directly compete with angiotensin-converting enzyme 2 for binding. Six to 10 antibodies can be assessed in parallel. This approach has been shown to determine escape mutants that are consistent with more laborious SARS-CoV-2 pseudoneutralization assays. For complete details on the use and execution of this protocol, please refer to Francino-Urdaniz et al. (2021).
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spelling pubmed-84552472021-09-22 Identification of SARS-CoV-2 S RBD escape mutants using yeast screening and deep mutational scanning Haas, Cyrus M. Francino-Urdaniz, Irene M. Steiner, Paul J. Whitehead, Timothy A. STAR Protoc Protocol Here, we describe a protocol to identify escape mutants on the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike (S) receptor-binding domain (RBD) using a yeast screen combined with deep mutational scanning. Over 90% of all potential single S RBD escape mutants can be identified for monoclonal antibodies that directly compete with angiotensin-converting enzyme 2 for binding. Six to 10 antibodies can be assessed in parallel. This approach has been shown to determine escape mutants that are consistent with more laborious SARS-CoV-2 pseudoneutralization assays. For complete details on the use and execution of this protocol, please refer to Francino-Urdaniz et al. (2021). Elsevier 2021-09-22 /pmc/articles/PMC8455247/ /pubmed/34568839 http://dx.doi.org/10.1016/j.xpro.2021.100869 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Haas, Cyrus M.
Francino-Urdaniz, Irene M.
Steiner, Paul J.
Whitehead, Timothy A.
Identification of SARS-CoV-2 S RBD escape mutants using yeast screening and deep mutational scanning
title Identification of SARS-CoV-2 S RBD escape mutants using yeast screening and deep mutational scanning
title_full Identification of SARS-CoV-2 S RBD escape mutants using yeast screening and deep mutational scanning
title_fullStr Identification of SARS-CoV-2 S RBD escape mutants using yeast screening and deep mutational scanning
title_full_unstemmed Identification of SARS-CoV-2 S RBD escape mutants using yeast screening and deep mutational scanning
title_short Identification of SARS-CoV-2 S RBD escape mutants using yeast screening and deep mutational scanning
title_sort identification of sars-cov-2 s rbd escape mutants using yeast screening and deep mutational scanning
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8455247/
https://www.ncbi.nlm.nih.gov/pubmed/34568839
http://dx.doi.org/10.1016/j.xpro.2021.100869
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