Rapid development of neutralizing and diagnostic SARS-COV-2 mouse monoclonal antibodies.
The need for high-affinity, SARS-CoV-2-specific monoclonal antibodies (mAbs) is critical in the face of the global COVID-19 pandemic, as such reagents can have important diagnostic, research, and therapeutic applications. Of greatest interest is the?~?300 amino acid receptor binding domain (RBD) within the S1 subunit of the spike protein because of ... its key interaction with the human angiotensin converting enzyme 2 (hACE2) receptor present on many cell types, especially lung epithelial cells. We report here the development and functional characterization of 29 nM-affinity mouse SARS-CoV-2 mAbs created by an accelerated immunization and hybridoma screening process. Differing functions, including binding of diverse protein epitopes, viral neutralization, impact on RBD-hACE2 binding, and immunohistochemical staining of infected lung tissue, were correlated with variable gene usage and sequence.
Mesh Terms:
Animals, Antibodies, Monoclonal, Antibodies, Neutralizing, Antibodies, Viral, COVID-19, COVID-19 Serological Testing, Epitopes, Female, Humans, Immunization, Mice, Mice, Inbred BALB C, Models, Molecular, SARS-CoV-2, Spike Glycoprotein, Coronavirus
Animals, Antibodies, Monoclonal, Antibodies, Neutralizing, Antibodies, Viral, COVID-19, COVID-19 Serological Testing, Epitopes, Female, Humans, Immunization, Mice, Mice, Inbred BALB C, Models, Molecular, SARS-CoV-2, Spike Glycoprotein, Coronavirus
Sci Rep
Date: May. 06, 2021
PubMed ID: 33958613
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