<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Long Y</submitter><funding>Chongqing Medical University</funding><pagination>152-158</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8289697</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>571</volume><pubmed_abstract>Potent neutralizing antibodies (Abs) have been proven with therapeutic efficacy for the intervention against SARS-CoV-2. Majority of these Abs function by directly interfering with the virus entry to host cells. Here, we identified a receptor binding domain (RBD) specific monoclonal Ab (mAb) 82A6 with efficient neutralizing potency against authentic SARS-CoV-2 virus. As most Abs targeting the non-receptor binding motif (RBM) region, 82A6 was incapable to block the RBD-ACE2 interaction. In particular, it actively promoted the S1 subunit shedding from the S protein, which may lead to effective reduction of intact SARS-CoV-2 viruses. Importantly, it could block potential syncytia formation associated with post-infectious cell surface expression of S proteins. Our study evidenced a RBD specific Ab with unique beneficial efficacy against SARS-CoV-2 infection, which might bring informative significance to understand the collective effects of neutralizing Abs elicited in COVID-19 patients.</pubmed_abstract><journal>Biochemical and biophysical research communications</journal><pubmed_title>A non-RBM targeted RBD specific antibody neutralizes SARS-CoV-2 inducing S1 shedding.</pubmed_title><pmcid>PMC8289697</pmcid><funding_grant_id>X4457</funding_grant_id><pubmed_authors>Hu C</pubmed_authors><pubmed_authors>Li S</pubmed_authors><pubmed_authors>Jin A</pubmed_authors><pubmed_authors>Long Y</pubmed_authors><pubmed_authors>Li T</pubmed_authors><pubmed_authors>Zhang H</pubmed_authors><pubmed_authors>Song S</pubmed_authors><pubmed_authors>Luo F</pubmed_authors><pubmed_authors>Han X</pubmed_authors><pubmed_authors>Wang W</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Zhang B</pubmed_authors></additional><is_claimable>false</is_claimable><name>A non-RBM targeted RBD specific antibody neutralizes SARS-CoV-2 inducing S1 shedding.</name><description>Potent neutralizing antibodies (Abs) have been proven with therapeutic efficacy for the intervention against SARS-CoV-2. Majority of these Abs function by directly interfering with the virus entry to host cells. Here, we identified a receptor binding domain (RBD) specific monoclonal Ab (mAb) 82A6 with efficient neutralizing potency against authentic SARS-CoV-2 virus. As most Abs targeting the non-receptor binding motif (RBM) region, 82A6 was incapable to block the RBD-ACE2 interaction. In particular, it actively promoted the S1 subunit shedding from the S protein, which may lead to effective reduction of intact SARS-CoV-2 viruses. Importantly, it could block potential syncytia formation associated with post-infectious cell surface expression of S proteins. Our study evidenced a RBD specific Ab with unique beneficial efficacy against SARS-CoV-2 infection, which might bring informative significance to understand the collective effects of neutralizing Abs elicited in COVID-19 patients.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Sep</publication><modification>2025-04-26T00:30:34.785Z</modification><creation>2025-04-06T09:40:45.931Z</creation></dates><accession>S-EPMC8289697</accession><cross_references><pubmed>34325131</pubmed><doi>10.1016/j.bbrc.2021.07.062</doi></cross_references></HashMap>