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4FQH

Crystal Structure of Fab CR9114

4FQH の概要
エントリーDOI10.2210/pdb4fqh/pdb
関連するPDBエントリー4FNK 4FQI 4FQJ 4FQK 4FQL 4FQM 4FQV 4FQY
分子名称antibody CR9114 heavy chain, antibody CR9114 light chain, 1,2-ETHANEDIOL, ... (5 entities in total)
機能のキーワードneutralizing antibodies, antibody affinity, antigens, epitope, glycosylation, hemagglutinin glycoproteins, immunoglobulin fab fragment, influenza virus, influenza vaccines, membrane fusion, immune system
由来する生物種Homo sapiens (human)
詳細
タンパク質・核酸の鎖数4
化学式量合計95085.21
構造登録者
Dreyfus, C.,Wilson, I.A. (登録日: 2012-06-25, 公開日: 2012-08-22, 最終更新日: 2024-11-27)
主引用文献Dreyfus, C.,Laursen, N.S.,Kwaks, T.,Zuijdgeest, D.,Khayat, R.,Ekiert, D.C.,Lee, J.H.,Metlagel, Z.,Bujny, M.V.,Jongeneelen, M.,van der Vlugt, R.,Lamrani, M.,Korse, H.J.,Geelen, E.,Sahin, O.,Sieuwerts, M.,Brakenhoff, J.P.,Vogels, R.,Li, O.T.,Poon, L.L.,Peiris, M.,Koudstaal, W.,Ward, A.B.,Wilson, I.A.,Goudsmit, J.,Friesen, R.H.
Highly conserved protective epitopes on influenza B viruses.
Science, 337:1343-1348, 2012
Cited by
PubMed Abstract: Identification of broadly neutralizing antibodies against influenza A viruses has raised hopes for the development of monoclonal antibody-based immunotherapy and "universal" vaccines for influenza. However, a substantial part of the annual flu burden is caused by two cocirculating, antigenically distinct lineages of influenza B viruses. Here, we report human monoclonal antibodies, CR8033, CR8071, and CR9114, that protect mice against lethal challenge from both lineages. Antibodies CR8033 and CR8071 recognize distinct conserved epitopes in the head region of the influenza B hemagglutinin (HA), whereas CR9114 binds a conserved epitope in the HA stem and protects against lethal challenge with influenza A and B viruses. These antibodies may inform on development of monoclonal antibody-based treatments and a universal flu vaccine for all influenza A and B viruses.
PubMed: 22878502
DOI: 10.1126/science.1222908
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.05 Å)
構造検証レポート
Validation report summary of 4fqh
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2025-07-30に公開中

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