7TM0

SARS-CoV-2 S B.1.1.529 Omicron variant + S309 + S2L20 Global Refinement

7TM0 の概要

• エントリーDOI: 10.2210/pdb7tm0/pdb
• 関連するPDBエントリー: 7TLY 7TLZ 7TM0 7TN0
• EMDBエントリー: 25990 25991 25992 25993
• 分子名称: Spike glycoprotein, S2L20 Fab light chain, S2L20 Fab heavy chain, ... (7 entities in total)
• 機能のキーワード: omicron, sars-cov-2, covid, b.1.529, antibody, fab, s309, sotrovimab, s2l20, virus, structural genomics, seattle structural genomics center for infectious disease, ssgcid
• 由来する生物種: Severe acute respiratory syndrome coronavirus 2; 詳細
• タンパク質・核酸の鎖数: 15
• 化学式量合計: 587632.57

構造登録者

McCallum, M.,Veesler, D.,Seattle Structural Genomics Center for Infectious Disease (SSGCID) (登録日: 2022-01-19, 公開日: 2022-02-02, 最終更新日: 2025-06-04)

主引用文献

McCallum, M.,Czudnochowski, N.,Rosen, L.E.,Zepeda, S.K.,Bowen, J.E.,Walls, A.C.,Hauser, K.,Joshi, A.,Stewart, C.,Dillen, J.R.,Powell, A.E.,Croll, T.I.,Nix, J.,Virgin, H.W.,Corti, D.,Snell, G.,Veesler, D.
Structural basis of SARS-CoV-2 Omicron immune evasion and receptor engagement.
Science, 375:864-868, 2022

PubMed Abstract: The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron variant of concern evades antibody-mediated immunity that comes from vaccination or infection with earlier variants due to accumulation of numerous spike mutations. To understand the Omicron antigenic shift, we determined cryo-electron microscopy and x-ray crystal structures of the spike protein and the receptor-binding domain bound to the broadly neutralizing sarbecovirus monoclonal antibody (mAb) S309 (the parent mAb of sotrovimab) and to the human ACE2 receptor. We provide a blueprint for understanding the marked reduction of binding of other therapeutic mAbs that leads to dampened neutralizing activity. Remodeling of interactions between the Omicron receptor-binding domain and human ACE2 likely explains the enhanced affinity for the host receptor relative to the ancestral virus.

PubMed: 35076256
DOI: 10.1126/science.abn8652

実験手法

ELECTRON MICROSCOPY (3.1 Å)