| Literature DB >> 35489332 |
Crystal Sao-Fong Cheung1, Jason Gorman1, Sarah F Andrews1, Reda Rawi1, Mateo Reveiz1, Chen-Hsiang Shen1, Yiran Wang1, Darcy R Harris1, Alexandra F Nazzari1, Adam S Olia1, Julie Raab1, I-Ting Teng1, Raffaello Verardi1, Shuishu Wang1, Yongping Yang1, Gwo-Yu Chuang1, Adrian B McDermott1, Tongqing Zhou1, Peter D Kwong2.
Abstract
Several influenza antibodies with broad group 2 neutralization have recently been isolated. Here, we analyze the structure, class, and binding of one of these antibodies from an H7N9 vaccine trial, 315-19-1D12. The cryo-EM structure of 315-19-1D12 Fab in complex with the hemagglutinin (HA) trimer revealed the antibody to recognize the helix A region of the HA stem, at the supersite of vulnerability recognized by group 1-specific and by cross-group-neutralizing antibodies. 315-19-1D12 was derived from HV1-2 and KV2-28 genes and appeared to form a new antibody class. Bioinformatic analysis indicated its group 2 neutralization specificity to be a consequence of four key residue positions. We specifically tested the impact of the group 1-specific N33 glycan, which decreased but did not abolish group 2 binding of 315-19-1D12. Overall, this study highlights the recognition of a broad group 2-neutralizing antibody, revealing unexpected diversity in neutralization specificity for antibodies that recognize the HA stem supersite. Published by Elsevier Ltd.Entities:
Keywords: antibody class; hemagglutinin; influenza; neutralizing antibodies; stem supersite
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Year: 2022 PMID: 35489332 PMCID: PMC9271601 DOI: 10.1016/j.str.2022.04.003
Source DB: PubMed Journal: Structure ISSN: 0969-2126 Impact factor: 5.871