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

https://doi.org/10.1016/j.bbrc.2021.07.062Get rights and content

Highlights

  • 82A6 could efficiently neutralize authentic SARS-CoV-2 virus with high binding affinity.

  • S334-353 might represent an essential site within the non-RBM region for the recognition of 82A6.

  • 82A6 triggered S1 shedding with high efficiency.

  • 82A6 could significantly block syncytia formation.

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.

Keywords

COVID-19
SARS-CoV-2
Receptor binding motif
Neutralizing antibody
S1 shedding
Syncytia

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1

The two co-first authors contributed equally to this work.

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