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6NB7

SARS-CoV complex with human neutralizing S230 antibody Fab fragment (state 2)

6NB7 の概要
エントリーDOI10.2210/pdb6nb7/pdb
関連するPDBエントリー6NB3 6NB4 6NB5 6NB6 6NB8
EMDBエントリー0401 0402 0403 0404
分子名称Spike glycoprotein, S230 heavy chain, S230 light chain, ... (9 entities in total)
機能のキーワードcoronavirus spike glycoprotein, mers-cov, sars-cov, human neutralizing antibodies, structural genomics, seattle structural genomics center for infectious disease, ssgcid, virus
由来する生物種SARS coronavirus (SARS-CoV)
詳細
タンパク質・核酸の鎖数9
化学式量合計526244.38
構造登録者
主引用文献Walls, A.C.,Xiong, X.,Park, Y.J.,Tortorici, M.A.,Snijder, J.,Quispe, J.,Cameroni, E.,Gopal, R.,Dai, M.,Lanzavecchia, A.,Zambon, M.,Rey, F.A.,Corti, D.,Veesler, D.
Unexpected Receptor Functional Mimicry Elucidates Activation of Coronavirus Fusion.
Cell, 176:1026-1039.e15, 2019
Cited by
PubMed Abstract: Recent outbreaks of severe acute respiratory syndrome and Middle East respiratory syndrome, along with the threat of a future coronavirus-mediated pandemic, underscore the importance of finding ways to combat these viruses. The trimeric spike transmembrane glycoprotein S mediates entry into host cells and is the major target of neutralizing antibodies. To understand the humoral immune response elicited upon natural infections with coronaviruses, we structurally characterized the SARS-CoV and MERS-CoV S glycoproteins in complex with neutralizing antibodies isolated from human survivors. Although the two antibodies studied blocked attachment to the host cell receptor, only the anti-SARS-CoV S antibody triggered fusogenic conformational changes via receptor functional mimicry. These results provide a structural framework for understanding coronavirus neutralization by human antibodies and shed light on activation of coronavirus membrane fusion, which takes place through a receptor-driven ratcheting mechanism.
PubMed: 30712865
DOI: 10.1016/j.cell.2018.12.028
主引用文献が同じPDBエントリー
実験手法
ELECTRON MICROSCOPY (4.5 Å)
構造検証レポート
Validation report summary of 6nb7
検証レポート(詳細版)ダウンロードをダウンロード

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件を2026-03-04に公開中

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