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Potent mouse monoclonal antibodies that block SARS-CoV-2 infection
Coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has developed into a global pandemic since its first outbreak in the winter of 2019. An extensive investigation of SARS-CoV-2 is critical for disease control. Various recombinant monoclonal a...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Biochemistry and Molecular Biology
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7846482/ https://www.ncbi.nlm.nih.gov/pubmed/33524396 http://dx.doi.org/10.1016/j.jbc.2021.100346 |
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author | Guo, Youjia Kawaguchi, Atsushi Takeshita, Masaru Sekiya, Takeshi Hirohama, Mikako Yamashita, Akio Siomi, Haruhiko Murano, Kensaku |
author_facet | Guo, Youjia Kawaguchi, Atsushi Takeshita, Masaru Sekiya, Takeshi Hirohama, Mikako Yamashita, Akio Siomi, Haruhiko Murano, Kensaku |
author_sort | Guo, Youjia |
collection | PubMed |
description | Coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has developed into a global pandemic since its first outbreak in the winter of 2019. An extensive investigation of SARS-CoV-2 is critical for disease control. Various recombinant monoclonal antibodies of human origin that neutralize SARS-CoV-2 infection have been isolated from convalescent patients and will be applied as therapies and prophylaxis. However, the need for dedicated monoclonal antibodies suitable for molecular pathology research is not fully addressed. Here, we produced six mouse anti-SARS-CoV-2 spike monoclonal antibodies that not only exhibit robust performance in immunoassays including western blotting, ELISA, immunofluorescence, and immunoprecipitation, but also demonstrate neutralizing activity against SARS-CoV-2 infection to VeroE6/TMPRSS2 cells. Due to their mouse origin, our monoclonal antibodies are compatible with the experimental immunoassay setups commonly used in basic molecular biology research laboratories, providing a useful tool for future research. Furthermore, in the hope of applying the antibodies of clinical setting, we determined the variable regions of the antibodies and used them to produce recombinant human/mouse chimeric antibodies. |
format | Online Article Text |
id | pubmed-7846482 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Society for Biochemistry and Molecular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-78464822021-02-01 Potent mouse monoclonal antibodies that block SARS-CoV-2 infection Guo, Youjia Kawaguchi, Atsushi Takeshita, Masaru Sekiya, Takeshi Hirohama, Mikako Yamashita, Akio Siomi, Haruhiko Murano, Kensaku J Biol Chem Accelerated Communication Coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has developed into a global pandemic since its first outbreak in the winter of 2019. An extensive investigation of SARS-CoV-2 is critical for disease control. Various recombinant monoclonal antibodies of human origin that neutralize SARS-CoV-2 infection have been isolated from convalescent patients and will be applied as therapies and prophylaxis. However, the need for dedicated monoclonal antibodies suitable for molecular pathology research is not fully addressed. Here, we produced six mouse anti-SARS-CoV-2 spike monoclonal antibodies that not only exhibit robust performance in immunoassays including western blotting, ELISA, immunofluorescence, and immunoprecipitation, but also demonstrate neutralizing activity against SARS-CoV-2 infection to VeroE6/TMPRSS2 cells. Due to their mouse origin, our monoclonal antibodies are compatible with the experimental immunoassay setups commonly used in basic molecular biology research laboratories, providing a useful tool for future research. Furthermore, in the hope of applying the antibodies of clinical setting, we determined the variable regions of the antibodies and used them to produce recombinant human/mouse chimeric antibodies. American Society for Biochemistry and Molecular Biology 2021-01-30 /pmc/articles/PMC7846482/ /pubmed/33524396 http://dx.doi.org/10.1016/j.jbc.2021.100346 Text en © 2021 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Accelerated Communication Guo, Youjia Kawaguchi, Atsushi Takeshita, Masaru Sekiya, Takeshi Hirohama, Mikako Yamashita, Akio Siomi, Haruhiko Murano, Kensaku Potent mouse monoclonal antibodies that block SARS-CoV-2 infection |
title | Potent mouse monoclonal antibodies that block SARS-CoV-2 infection |
title_full | Potent mouse monoclonal antibodies that block SARS-CoV-2 infection |
title_fullStr | Potent mouse monoclonal antibodies that block SARS-CoV-2 infection |
title_full_unstemmed | Potent mouse monoclonal antibodies that block SARS-CoV-2 infection |
title_short | Potent mouse monoclonal antibodies that block SARS-CoV-2 infection |
title_sort | potent mouse monoclonal antibodies that block sars-cov-2 infection |
topic | Accelerated Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7846482/ https://www.ncbi.nlm.nih.gov/pubmed/33524396 http://dx.doi.org/10.1016/j.jbc.2021.100346 |
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