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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...

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Autores principales: Guo, Youjia, Kawaguchi, Atsushi, Takeshita, Masaru, Sekiya, Takeshi, Hirohama, Mikako, Yamashita, Akio, Siomi, Haruhiko, Murano, Kensaku
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2021
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.
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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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