7RW2
Cryo-EM structure of NTD-directed neutralizing antibody 5-7 in complex with prefusion SARS-CoV-2 spike glycoprotein
「7N01」から置き換えられました7RW2 の概要
| エントリーDOI | 10.2210/pdb7rw2/pdb |
| EMDBエントリー | 24708 |
| 分子名称 | Spike glycoprotein, 5-7 heavy chain, 5-7 light chain, ... (5 entities in total) |
| 機能のキーワード | neutralizing antibody, fusion protein, spike glycoprotein, covid-19, n-terminal domain, ntd, 5-7, viral protein-immune system complex, viral protein/immune system |
| 由来する生物種 | Severe acute respiratory syndrome coronavirus 2 (2019-nCoV) 詳細 |
| タンパク質・核酸の鎖数 | 9 |
| 化学式量合計 | 591078.99 |
| 構造登録者 | |
| 主引用文献 | Cerutti, G.,Guo, Y.,Wang, P.,Nair, M.S.,Wang, M.,Huang, Y.,Yu, J.,Liu, L.,Katsamba, P.S.,Bahna, F.,Reddem, E.R.,Kwong, P.D.,Ho, D.D.,Sheng, Z.,Shapiro, L. Neutralizing antibody 5-7 defines a distinct site of vulnerability in SARS-CoV-2 spike N-terminal domain. Cell Rep, 37:109928-109928, 2021 Cited by PubMed Abstract: Antibodies that potently neutralize SARS-CoV-2 target mainly the receptor-binding domain or the N-terminal domain (NTD). Over a dozen potently neutralizing NTD-directed antibodies have been studied structurally, and all target a single antigenic supersite in NTD (site 1). Here, we report the cryo-EM structure of a potent NTD-directed neutralizing antibody 5-7, which recognizes a site distinct from other potently neutralizing antibodies, inserting a binding loop into an exposed hydrophobic pocket between the two sheets of the NTD β sandwich. Interestingly, this pocket was previously identified as the binding site for hydrophobic molecules, including heme metabolites, but we observe that their presence does not substantially impede 5-7 recognition. Mirroring its distinctive binding, antibody 5-7 retains neutralization potency with many variants of concern (VOCs). Overall, we reveal that a hydrophobic pocket in NTD proposed for immune evasion can be used by the immune system for recognition. PubMed: 34706271DOI: 10.1016/j.celrep.2021.109928 主引用文献が同じPDBエントリー |
| 実験手法 | ELECTRON MICROSCOPY (3.5 Å) |
構造検証レポート
検証レポート(詳細版)
をダウンロード






