| Literature DB >> 30625326 |
Xishan Lu1, Haixia Xiao1, Shihua Li2, Xuefei Pang1, Jian Song2, Sheng Liu2, Huijun Cheng3, Yan Li2, Xiangxi Wang4, Chaobin Huang1, Tianling Guo1, Jan Ter Meulen5, Stephane Daffis5, Jinghua Yan6, Lianpan Dai3, Zihe Rao4, Hans-Dieter Klenk5, Jianxun Qi2, Yi Shi2, George F Gao7.
Abstract
Yellow fever virus (YFV), a deadly human pathogen, is the prototype of the genus Flavivirus. Recently, YFV re-emerged in Africa and Brazil, leading to hundreds of deaths, with some cases imported to China. Prophylactic or therapeutic countermeasures are urgently needed. Previously, several human monoclonal antibodies against YFV were screened out by phage display. Here, we find that one of them, 5A, exhibits high neutralizing potency and good protection. Crystallographic analysis of the YFV envelope (E) protein in its pre- and post-fusion states shows conformations similar to those observed in other E proteins of flaviviruses. Furthermore, the structures of 5A in complex with the E protein in both states are resolved, revealing an invariant recognition site. Structural analysis and functional data suggest that 5A has high neutralization potency because it interferes with virus entry by preventing both virus attachment and fusion. These findings will be instrumental for immunogen or inhibitor design.Entities:
Keywords: crystal structure; envelope protein; epitope; flavivirus; neutralizing monoclonal antibody; postfusion; prefusion; yellow fever virus
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Year: 2019 PMID: 30625326 DOI: 10.1016/j.celrep.2018.12.065
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423