7R6X

SARS-CoV-2 spike receptor-binding domain (RBD) in complex with S2E12 Fab, S309 Fab, and S304 Fab

7R6X の概要

• エントリーDOI: 10.2210/pdb7r6x/pdb
• 関連するPDBエントリー: 7M7W 7R6W
• 分子名称: Monoclonal antibody S304 Fab light chain, Monoclonal antibody S304 Fab heavy chain, Spike protein S1, ... (10 entities in total)
• 機能のキーワード: covid-19, sars-cov-2, neutralizing monoclonal antibody, viral protein-immune system complex, viral protein/immune system
• 由来する生物種: Homo sapiens (Human); 詳細
• タンパク質・核酸の鎖数: 7
• 化学式量合計: 167174.98

構造登録者

Snell, G.,Czudnochowski, N.,Croll, T.I.,Nix, J.C.,Corti, D.,Cameroni, E.,Pinto, D.,Beltramello, M. (登録日: 2021-06-23, 公開日: 2021-07-21, 最終更新日: 2024-10-16)

主引用文献

Starr, T.N.,Czudnochowski, N.,Liu, Z.,Zatta, F.,Park, Y.J.,Addetia, A.,Pinto, D.,Beltramello, M.,Hernandez, P.,Greaney, A.J.,Marzi, R.,Glass, W.G.,Zhang, I.,Dingens, A.S.,Bowen, J.E.,Tortorici, M.A.,Walls, A.C.,Wojcechowskyj, J.A.,De Marco, A.,Rosen, L.E.,Zhou, J.,Montiel-Ruiz, M.,Kaiser, H.,Dillen, J.R.,Tucker, H.,Bassi, J.,Silacci-Fregni, C.,Housley, M.P.,di Iulio, J.,Lombardo, G.,Agostini, M.,Sprugasci, N.,Culap, K.,Jaconi, S.,Meury, M.,Dellota Jr., E.,Abdelnabi, R.,Foo, S.C.,Cameroni, E.,Stumpf, S.,Croll, T.I.,Nix, J.C.,Havenar-Daughton, C.,Piccoli, L.,Benigni, F.,Neyts, J.,Telenti, A.,Lempp, F.A.,Pizzuto, M.S.,Chodera, J.D.,Hebner, C.M.,Virgin, H.W.,Whelan, S.P.J.,Veesler, D.,Corti, D.,Bloom, J.D.,Snell, G.
SARS-CoV-2 RBD antibodies that maximize breadth and resistance to escape.
Nature, 597:97-102, 2021

PubMed Abstract: An ideal therapeutic anti-SARS-CoV-2 antibody would resist viral escape, have activity against diverse sarbecoviruses, and be highly protective through viral neutralization and effector functions. Understanding how these properties relate to each other and vary across epitopes would aid the development of therapeutic antibodies and guide vaccine design. Here we comprehensively characterize escape, breadth and potency across a panel of SARS-CoV-2 antibodies targeting the receptor-binding domain (RBD). Despite a trade-off between in vitro neutralization potency and breadth of sarbecovirus binding, we identify neutralizing antibodies with exceptional sarbecovirus breadth and a corresponding resistance to SARS-CoV-2 escape. One of these antibodies, S2H97, binds with high affinity across all sarbecovirus clades to a cryptic epitope and prophylactically protects hamsters from viral challenge. Antibodies that target the angiotensin-converting enzyme 2 (ACE2) receptor-binding motif (RBM) typically have poor breadth and are readily escaped by mutations despite high neutralization potency. Nevertheless, we also characterize a potent RBM antibody (S2E12) with breadth across sarbecoviruses related to SARS-CoV-2 and a high barrier to viral escape. These data highlight principles underlying variation in escape, breadth and potency among antibodies that target the RBD, and identify epitopes and features to prioritize for therapeutic development against the current and potential future pandemics.

PubMed: 34261126
DOI: 10.1038/s41586-021-03807-6

実験手法

X-RAY DIFFRACTION (2.95 Å)