Unknown

Dataset Information

0

Human antibody BD-218 has broad neutralizing activity against concerning variants of SARS-CoV-2.


ABSTRACT: As SARS-CoV-2 variants of concern (VOC) reduce the effectiveness of existing anti-COVID therapeutics, it is increasingly critical to identify highly potent neutralizing antibodies (nAbs) that bind to conserved regions across multiple variants, especially beta, delta, and omicron variants. Using single-cell sequencing with biochemical methods and pseudo-typed virus neutralization experiments, here we report the characterization of a potent nAb BD-218, identified from an early screen of patients recovering from the original virus. We have determined the cryo-EM structure of the BD-218/spike protein complex to define its epitope in detail, which revealed that BD-218 interacts with a novel epitope on the receptor-binding domain (RBD) of the spike protein. We concluded that BD-218 is a highly effective and broadly active nAb against SARS-CoV-2 variants with promising potential for therapeutic development.

SUBMITTER: Wang B 

PROVIDER: S-EPMC9747686 | biostudies-literature | 2023 Feb

REPOSITORIES: biostudies-literature

altmetric image

Publications

Human antibody BD-218 has broad neutralizing activity against concerning variants of SARS-CoV-2.

Wang Bo B   Xu Hua H   Liang Zi-Teng ZT   Zhao Tian-Ning TN   Zhang Xin X   Peng Tian-Bo TB   Wang You-Chun YC   Su Xiao-Dong XD  

International journal of biological macromolecules 20221214


As SARS-CoV-2 variants of concern (VOC) reduce the effectiveness of existing anti-COVID therapeutics, it is increasingly critical to identify highly potent neutralizing antibodies (nAbs) that bind to conserved regions across multiple variants, especially beta, delta, and omicron variants. Using single-cell sequencing with biochemical methods and pseudo-typed virus neutralization experiments, here we report the characterization of a potent nAb BD-218, identified from an early screen of patients r  ...[more]

Similar Datasets

| S-EPMC10461085 | biostudies-literature
| S-EPMC10749193 | biostudies-literature
| S-EPMC10693169 | biostudies-literature
| S-EPMC8255729 | biostudies-literature
| S-EPMC8765073 | biostudies-literature
| S-EPMC8710476 | biostudies-literature
| S-EPMC8878391 | biostudies-literature
| S-EPMC8371079 | biostudies-literature
| S-EPMC10071473 | biostudies-literature
| S-EPMC9201380 | biostudies-literature