8E1G
SARS-CoV-2 RBD in complex with Omicron-neutralizing antibody 2A10
8E1G の概要
エントリーDOI | 10.2210/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: 37083327DOI: 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) |
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