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A non-RBM targeted RBD specific antibody neutralizes SARS-CoV-2 inducing S1 shedding.


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.

SUBMITTER: Long Y 

PROVIDER: S-EPMC8289697 | biostudies-literature | 2021 Sep

REPOSITORIES: biostudies-literature

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A non-RBM targeted RBD specific antibody neutralizes SARS-CoV-2 inducing S1 shedding.

Long Yingyi Y   Song Shuyi S   Luo Feiyang F   Han Xiaojian X   Hu Chao C   Wang Yingming Y   Li Shenglong S   Wang Wang W   Zhang Huajun H   Zhang Bo B   Li Tingting T   Jin Aishun A  

Biochemical and biophysical research communications 20210720


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 partic  ...[more]

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