5WTH
Cryo-EM structure for Hepatitis A virus complexed with FAB
5WTH の概要
| エントリーDOI | 10.2210/pdb5wth/pdb |
| 関連するPDBエントリー | 5WTE 5WTF |
| EMDBエントリー | 6686 6687 6688 |
| 分子名称 | Polyprotein, VP2, VP3, ... (5 entities in total) |
| 機能のキーワード | hav, neutralizing mechanism, receptor recognition, viral entry, virus |
| 由来する生物種 | Hepatovirus A 詳細 |
| タンパク質・核酸の鎖数 | 5 |
| 化学式量合計 | 130512.68 |
| 構造登録者 | |
| 主引用文献 | Wang, X.,Zhu, L.,Dang, M.,Hu, Z.,Gao, Q.,Yuan, S.,Sun, Y.,Zhang, B.,Ren, J.,Kotecha, A.,Walter, T.S.,Wang, J.,Fry, E.E.,Stuart, D.I.,Rao, Z. Potent neutralization of hepatitis A virus reveals a receptor mimic mechanism and the receptor recognition site Proc. Natl. Acad. Sci. U.S.A., 114:770-775, 2017 Cited by PubMed Abstract: Hepatitis A virus (HAV) infects ∼1.4 million people annually and, although there is a vaccine, there are no licensed therapeutic drugs. HAV is unusually stable (making disinfection problematic) and little is known of how it enters cells and releases its RNA. Here we report a potent HAV-specific monoclonal antibody, R10, which neutralizes HAV infection by blocking attachment to the host cell. High-resolution cryo-EM structures of HAV full and empty particles and of the complex of HAV with R10 Fab reveal the atomic details of antibody binding and point to a receptor recognition site at the pentamer interface. These results, together with our observation that the R10 Fab destabilizes the capsid, suggest the use of a receptor mimic mechanism to neutralize virus infection, providing new opportunities for therapeutic intervention. PubMed: 28074040DOI: 10.1073/pnas.1616502114 主引用文献が同じPDBエントリー |
| 実験手法 | ELECTRON MICROSCOPY (4.2 Å) |
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