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Antigenic mapping reveals sites of vulnerability on α-HCoV spike protein.


ABSTRACT: Understanding the antigenic signatures of all human coronaviruses (HCoVs) Spike (S) proteins is imperative for pan-HCoV epitopes identification and broadly effective vaccine development. To depict the currently elusive antigenic signatures of α-HCoVs S proteins, we isolated a panel of antibodies against the HCoV-229E S protein and characterized their epitopes and neutralizing potential. We found that the N-terminal domain of HCoV-229E S protein is antigenically dominant wherein an antigenic supersite is present and appears conserved in HCoV-NL63, which holds potential to serve as a pan-α-HCoVs epitope. In the receptor binding domain, a neutralizing epitope is captured in the end distal to the receptor binding site, reminiscent of the locations of the SARS-CoV-2 RBD cryptic epitopes. We also identified a neutralizing antibody that recognizes the connector domain, thus representing the first S2-directed neutralizing antibody against α-HCoVs. The unraveled HCoVs S proteins antigenic similarities and variances among genera highlight the challenges faced by pan-HCoV vaccine design while supporting the feasibility of broadly effective vaccine development against a subset of HCoVs.

SUBMITTER: Xiang J 

PROVIDER: S-EPMC9636267 | biostudies-literature | 2022 Nov

REPOSITORIES: biostudies-literature

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Antigenic mapping reveals sites of vulnerability on α-HCoV spike protein.

Xiang Jiangchao J   Su Jie J   Lan Qiaoshuai Q   Zhao Wenwen W   Zhou Yu Y   Xu Youwei Y   Niu Jun J   Xia Shuai S   Qi Qilian Q   Sidhu Sachdev S   Lu Lu L   Miersch Shane S   Yang Bei B  

Communications biology 20221104 1


Understanding the antigenic signatures of all human coronaviruses (HCoVs) Spike (S) proteins is imperative for pan-HCoV epitopes identification and broadly effective vaccine development. To depict the currently elusive antigenic signatures of α-HCoVs S proteins, we isolated a panel of antibodies against the HCoV-229E S protein and characterized their epitopes and neutralizing potential. We found that the N-terminal domain of HCoV-229E S protein is antigenically dominant wherein an antigenic supe  ...[more]

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