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Mechanisms of SARS-CoV-2 neutralization by shark variable new antigen receptors elucidated through X-ray crystallography
Single-domain Variable New Antigen Receptors (VNARs) from the immune system of sharks are the smallest naturally occurring binding domains found in nature. Possessing flexible paratopes that can recognize protein motifs inaccessible to classical antibodies, VNARs have yet to be exploited for the dev...
Autores principales: | , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8677774/ https://www.ncbi.nlm.nih.gov/pubmed/34916516 http://dx.doi.org/10.1038/s41467-021-27611-y |
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author | Ubah, Obinna C. Lake, Eric W. Gunaratne, Gihan S. Gallant, Joseph P. Fernie, Marie Robertson, Austin J. Marchant, Jonathan S. Bold, Tyler D. Langlois, Ryan A. Matchett, William E. Thiede, Joshua M. Shi, Ke Yin, Lulu Moeller, Nicholas H. Banerjee, Surajit Ferguson, Laura Kovaleva, Marina Porter, Andrew J. Aihara, Hideki LeBeau, Aaron M. Barelle, Caroline J. |
author_facet | Ubah, Obinna C. Lake, Eric W. Gunaratne, Gihan S. Gallant, Joseph P. Fernie, Marie Robertson, Austin J. Marchant, Jonathan S. Bold, Tyler D. Langlois, Ryan A. Matchett, William E. Thiede, Joshua M. Shi, Ke Yin, Lulu Moeller, Nicholas H. Banerjee, Surajit Ferguson, Laura Kovaleva, Marina Porter, Andrew J. Aihara, Hideki LeBeau, Aaron M. Barelle, Caroline J. |
author_sort | Ubah, Obinna C. |
collection | PubMed |
description | Single-domain Variable New Antigen Receptors (VNARs) from the immune system of sharks are the smallest naturally occurring binding domains found in nature. Possessing flexible paratopes that can recognize protein motifs inaccessible to classical antibodies, VNARs have yet to be exploited for the development of SARS-CoV-2 therapeutics. Here, we detail the identification of a series of VNARs from a VNAR phage display library screened against the SARS-CoV-2 receptor binding domain (RBD). The ability of the VNARs to neutralize pseudotype and authentic live SARS-CoV-2 virus rivalled or exceeded that of full-length immunoglobulins and other single-domain antibodies. Crystallographic analysis of two VNARs found that they recognized separate epitopes on the RBD and had distinctly different mechanisms of virus neutralization unique to VNARs. Structural and biochemical data suggest that VNARs would be effective therapeutic agents against emerging SARS-CoV-2 mutants, including the Delta variant, and coronaviruses across multiple phylogenetic lineages. This study highlights the utility of VNARs as effective therapeutics against coronaviruses and may serve as a critical milestone for nearing a paradigm shift of the greater biologic landscape. |
format | Online Article Text |
id | pubmed-8677774 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-86777742022-01-04 Mechanisms of SARS-CoV-2 neutralization by shark variable new antigen receptors elucidated through X-ray crystallography Ubah, Obinna C. Lake, Eric W. Gunaratne, Gihan S. Gallant, Joseph P. Fernie, Marie Robertson, Austin J. Marchant, Jonathan S. Bold, Tyler D. Langlois, Ryan A. Matchett, William E. Thiede, Joshua M. Shi, Ke Yin, Lulu Moeller, Nicholas H. Banerjee, Surajit Ferguson, Laura Kovaleva, Marina Porter, Andrew J. Aihara, Hideki LeBeau, Aaron M. Barelle, Caroline J. Nat Commun Article Single-domain Variable New Antigen Receptors (VNARs) from the immune system of sharks are the smallest naturally occurring binding domains found in nature. Possessing flexible paratopes that can recognize protein motifs inaccessible to classical antibodies, VNARs have yet to be exploited for the development of SARS-CoV-2 therapeutics. Here, we detail the identification of a series of VNARs from a VNAR phage display library screened against the SARS-CoV-2 receptor binding domain (RBD). The ability of the VNARs to neutralize pseudotype and authentic live SARS-CoV-2 virus rivalled or exceeded that of full-length immunoglobulins and other single-domain antibodies. Crystallographic analysis of two VNARs found that they recognized separate epitopes on the RBD and had distinctly different mechanisms of virus neutralization unique to VNARs. Structural and biochemical data suggest that VNARs would be effective therapeutic agents against emerging SARS-CoV-2 mutants, including the Delta variant, and coronaviruses across multiple phylogenetic lineages. This study highlights the utility of VNARs as effective therapeutics against coronaviruses and may serve as a critical milestone for nearing a paradigm shift of the greater biologic landscape. Nature Publishing Group UK 2021-12-16 /pmc/articles/PMC8677774/ /pubmed/34916516 http://dx.doi.org/10.1038/s41467-021-27611-y Text en © The Author(s) 2021 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 Ubah, Obinna C. Lake, Eric W. Gunaratne, Gihan S. Gallant, Joseph P. Fernie, Marie Robertson, Austin J. Marchant, Jonathan S. Bold, Tyler D. Langlois, Ryan A. Matchett, William E. Thiede, Joshua M. Shi, Ke Yin, Lulu Moeller, Nicholas H. Banerjee, Surajit Ferguson, Laura Kovaleva, Marina Porter, Andrew J. Aihara, Hideki LeBeau, Aaron M. Barelle, Caroline J. Mechanisms of SARS-CoV-2 neutralization by shark variable new antigen receptors elucidated through X-ray crystallography |
title | Mechanisms of SARS-CoV-2 neutralization by shark variable new antigen receptors elucidated through X-ray crystallography |
title_full | Mechanisms of SARS-CoV-2 neutralization by shark variable new antigen receptors elucidated through X-ray crystallography |
title_fullStr | Mechanisms of SARS-CoV-2 neutralization by shark variable new antigen receptors elucidated through X-ray crystallography |
title_full_unstemmed | Mechanisms of SARS-CoV-2 neutralization by shark variable new antigen receptors elucidated through X-ray crystallography |
title_short | Mechanisms of SARS-CoV-2 neutralization by shark variable new antigen receptors elucidated through X-ray crystallography |
title_sort | mechanisms of sars-cov-2 neutralization by shark variable new antigen receptors elucidated through x-ray crystallography |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8677774/ https://www.ncbi.nlm.nih.gov/pubmed/34916516 http://dx.doi.org/10.1038/s41467-021-27611-y |
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