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Development of a SARS-CoV-2 nucleocapsid specific monoclonal antibody.
Terry, James S; Anderson, Loran Br; Scherman, Michael S; McAlister, Carley E; Perera, Rushika; Schountz, Tony; Geiss, Brian J.
  • Terry JS; Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, CO, USA.
  • Anderson LB; Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, CO, USA.
  • Scherman MS; Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, CO, USA.
  • McAlister CE; Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, CO, USA; Arthropod-borne and Infectious Diseases Laboratory, Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, CO, USA.
  • Perera R; Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, CO, USA; Arthropod-borne and Infectious Diseases Laboratory, Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, CO, USA.
  • Schountz T; Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, CO, USA; Arthropod-borne and Infectious Diseases Laboratory, Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, CO, USA.
  • Geiss BJ; Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, CO, USA; Arthropod-borne and Infectious Diseases Laboratory, Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, CO, USA; School of Biomedical Engineering, Colora
Virology ; 558: 28-37, 2021 06.
Article in English | MEDLINE | ID: covidwho-1057461
ABSTRACT
To help fight COVID-19, new molecular tools specifically targeting critical components of the causative agent of COVID-19, SARS-Coronavirus-2 (SARS-CoV-2), are desperately needed. The SARS-CoV-2 nucleocapsid protein is critical for viral replication, integral to viral particle assembly, and a major diagnostic marker for infection and immune protection. Currently the limited available antibody reagents targeting the nucleocapsid protein are not specific to SARS-CoV-2 nucleocapsid protein, and sequences for these antibodies are not publicly available. In this work we developed and characterized a series of new mouse monoclonal antibodies against the SARS-CoV-2 nucleocapsid protein, with a specific clone, mBG86, targeting only SARS-CoV-2 nucleocapsid protein. The monoclonal antibodies were validated in ELISA, Western blot, and immunofluorescence analyses. The variable regions from six select clones were cloned and sequenced, and preliminary epitope mapping of the sequenced clones was performed. Overall, these new antibody reagents will be of significant value in the fight against COVID-19.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Coronavirus Nucleocapsid Proteins / SARS-CoV-2 / COVID-19 / Antibodies, Monoclonal / Antibodies, Viral Type of study: Observational study / Prognostic study Limits: Animals / Female / Humans Language: English Journal: Virology Year: 2021 Document Type: Article Affiliation country: J.virol.2021.01.003

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Coronavirus Nucleocapsid Proteins / SARS-CoV-2 / COVID-19 / Antibodies, Monoclonal / Antibodies, Viral Type of study: Observational study / Prognostic study Limits: Animals / Female / Humans Language: English Journal: Virology Year: 2021 Document Type: Article Affiliation country: J.virol.2021.01.003