4.6 Article

Neutralizing Monoclonal Antibodies Inhibit SARS-CoV-2 Infection through Blocking Membrane Fusion

期刊

MICROBIOLOGY SPECTRUM
卷 10, 期 2, 页码 -

出版社

AMER SOC MICROBIOLOGY
DOI: 10.1128/spectrum.01814-21

关键词

neutralizing antibodies; SARS-CoV-2; spike (S) protein; S2 subunit; membrane fusion

资金

  1. Ministry of Science and Technology, Taiwan [MOST-110-2311-B-002-010, MOST109-2327-B-002-009]
  2. National Taiwan University [109L883703, 110L880802]

向作者/读者索取更多资源

This study identified four S2-specific neutralizing antibodies (nAbs) that inhibit SARS-CoV-2 infection by blocking S protein-mediated membrane fusion. These nAbs exhibited broad neutralizing activity against different variants of SARS-CoV-2. The discovery of these nAbs and their unique antigenic epitopes provides new opportunities for the development of COVID-19 therapeutics and vaccines.
Most of SARS-CoV-2 neutralizing antibodies (nAbs) targeted the receptor binding domain (RBD) of the SARS-CoV-2 spike (S) protein. However, mutations at RBD sequences found in the emerging SARS-CoV-2 variants greatly reduced the effectiveness of nAbs. Here we showed that four nAbs, S2-4D, S2-5D, S2-8D, and S24A, which recognized a conserved epitope in the S2 subunit of the S protein, can inhibit SARS-CoV-2 infection through blocking the S protein-mediated membrane fusion. Notably, these four nAbs exhibited broadly neutralizing activity against SARS-CoV-2 Alpha, Gamma, Delta, and Epsilon variants. Antisera collected from mice immunized with the identified epitope peptides of these four nAbs also exhibited potent virus neutralizing activity. Discovery of the 52-specific nAbs and their unique antigenic epitopes paves a new path for development of COVID-19 therapeutics and vaccines. IMPORTANCE The spike (S) protein on the surface of SARS-CoV-2 mediates receptor binding and virus-host cell membrane fusion during virus entry. Many neutralizing antibodies (nAbs), which targeted the receptor binding domain (RBD) of S protein, lost the neutralizing activity against the newly emerging SARS-CoV-2 variants with sequence mutations at the RBD. In contrast, the nAb against the highly conserved S2 subunit, which plays the key role in virus-host cell membrane fusion, was poorly discovered. We showed that four S2-specific nAbs, S2-4D, S2-SD, S2-8D, and S2-4A, inhibited SARS-CoV-2 infection through blocking the S protein-mediated membrane fusion. These nAbs exhibited broadly neutralizing activity against Alpha, Gamma, Delta, and Epsilon variants. Antisera induced by the identified epitope peptides also possessed potent neutralizing activity. This work not only unveiled the S2-specific nAbs but also discovered an immunodominant epitope in the S2 subunit that can be rationally designed as the broad-spectrum vaccine against the SARS-like coronaviruses.

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