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8EAY

HMPV F complex with 4I3 Fab

8EAY の概要
エントリーDOI10.2210/pdb8eay/pdb
EMDBエントリー27808 27990
分子名称Fusion glycoprotein F0, 4I3 heavy chain protein, 4I3 light chain protein (3 entities in total)
機能のキーワードhuman antibodies, rsv and mpv fusion protein, complex cryo-em structure, viral protein and antiviral protein, biosynthetic protein
由来する生物種Human metapneumovirus A (human)
詳細
タンパク質・核酸の鎖数3
化学式量合計69859.11
構造登録者
Wen, X.,Jardetzky, T.S. (登録日: 2022-08-30, 公開日: 2023-08-16, 最終更新日: 2024-11-13)
主引用文献Wen, X.,Suryadevara, N.,Kose, N.,Liu, J.,Zhan, X.,Handal, L.S.,Williamson, L.E.,Trivette, A.,Carnahan, R.H.,Jardetzky, T.S.,Crowe Jr., J.E.
Potent cross-neutralization of respiratory syncytial virus and human metapneumovirus through a structurally conserved antibody recognition mode.
Cell Host Microbe, 31:1288-1300.e6, 2023
Cited by
PubMed Abstract: Respiratory syncytial virus (RSV) and human metapneumovirus (hMPV) infections pose a significant health burden. Using pre-fusion conformation fusion (F) proteins, we isolated a panel of anti-F antibodies from a human donor. One antibody (RSV-199) potently cross-neutralized 8 RSV and hMPV strains by recognizing antigenic site III, which is partially conserved in RSV and hMPV F. Next, we determined the cryoelectron microscopy (cryo-EM) structures of RSV-199 bound to RSV F trimers, hMPV F monomers, and an unexpected dimeric form of hMPV F. These structures revealed how RSV-199 engages both RSV and hMPV F proteins through conserved interactions of the antibody heavy-chain variable region and how variability within heavy-chain complementarity-determining region 3 (HCDR3) can be accommodated at the F protein interface in site-III-directed antibodies. Furthermore, RSV-199 offered enhanced protection against RSV A and B strains and hMPV in cotton rats. These findings highlight the mechanisms of broad neutralization and therapeutic potential of RSV-199.
PubMed: 37516111
DOI: 10.1016/j.chom.2023.07.002
主引用文献が同じPDBエントリー
実験手法
ELECTRON MICROSCOPY (3.33 Å)
構造検証レポート
Validation report summary of 8eay
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2026-02-04に公開中

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