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8E1G

SARS-CoV-2 RBD in complex with Omicron-neutralizing antibody 2A10

8E1G の概要
エントリーDOI10.2210/pdb8e1g/pdb
分子名称2A10 Fab, heavy chain, 2A10 Fab, light chain, Spike protein S1, ... (4 entities in total)
機能のキーワードsars-cov-2, omicron, antibody, neutralizing, viral protein
由来する生物種Homo sapiens (human)
詳細
タンパク質・核酸の鎖数6
化学式量合計158344.71
構造登録者
Wasserman, H.,Hastie, K.M.,Buck, T.K.,Saphire, E.O. (登録日: 2022-08-10, 公開日: 2023-06-28, 最終更新日: 2024-11-13)
主引用文献Hastie, K.M.,Yu, X.,Ana-Sosa-Batiz, F.,Zyla, D.S.,Harkins, S.S.,Hariharan, C.,Wasserman, H.,Zandonatti, M.A.,Miller, R.,Maule, E.,Kim, K.,Valentine, K.M.,Shresta, S.,Saphire, E.O.
Potent Omicron-neutralizing antibodies isolated from a patient vaccinated 6 months before Omicron emergence.
Cell Rep, 42:112421-112421, 2023
Cited by
PubMed Abstract: Therapeutic antibodies are an important tool in the arsenal against coronavirus infection. However, most antibodies developed early in the pandemic have lost most or all efficacy against newly emergent strains of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), particularly those of the Omicron lineage. Here, we report the identification of a panel of vaccinee-derived antibodies that have broad-spectrum neutralization activity. Structural and biochemical characterization of the three broadest-spectrum antibodies reveal complementary footprints and differing requirements for avidity to overcome variant-associated mutations in their binding footprints. In the K18 mouse model of infection, these three antibodies exhibit protective efficacy against BA.1 and BA.2 infection. This study highlights the resilience and vulnerabilities of SARS-CoV-2 antibodies and provides road maps for further development of broad-spectrum therapeutics.
PubMed: 37083327
DOI: 10.1016/j.celrep.2023.112421
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.57 Å)
構造検証レポート
Validation report summary of 8e1g
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2025-04-02に公開中

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