8E6J

3H03 Fab in complex with influenza virus neuraminidase from A/Brevig Mission/1/1918 (H1N1)

8E6J の概要

• エントリーDOI: 10.2210/pdb8e6j/pdb
• EMDBエントリー: 27920
• 分子名称: Neuraminidase, 3H03 fragment antigen binding light chain, 3H03 fragment antigen binding heavy chain (3 entities in total)
• 機能のキーワード: influenza, monoclonal antibody, na, h1n1, cross-reactive antibody, viral protein
• 由来する生物種: Influenza A virus (A/Brevig Mission/1/1918(H1N1)); 詳細
• タンパク質・核酸の鎖数: 12
• 化学式量合計: 390290.30

構造登録者

Turner, H.L.,Ozorowski, G.,Ward, A.B. (登録日: 2022-08-22, 公開日: 2023-08-09, 最終更新日: 2024-10-09)

主引用文献

Hansen, L.,McMahon, M.,Turner, H.L.,Zhu, X.,Turner, J.S.,Ozorowski, G.,Stadlbauer, D.,Vahokoski, J.,Schmitz, A.J.,Rizk, A.A.,Alsoussi, W.B.,Strohmeier, S.,Yu, W.,Choreno-Parra, J.A.,Jimenez-Alvarez, L.,Cruz-Lagunas, A.,Zuniga, J.,Mudd, P.A.,Cox, R.J.,Wilson, I.A.,Ward, A.B.,Ellebedy, A.H.,Krammer, F.
Human anti-N1 monoclonal antibodies elicited by pandemic H1N1 virus infection broadly inhibit HxN1 viruses in vitro and in vivo.
Immunity, 56:1927-1938.e8, 2023

PubMed Abstract: Neuraminidase (NA) is one of the two influenza virus surface glycoproteins, and antibodies that target it are an independent correlate of protection. However, our current understanding of NA antigenicity is incomplete. Here, we describe human monoclonal antibodies (mAbs) from a patient with a pandemic H1N1 virus infection in 2009. Two mAbs exhibited broad reactivity and inhibited NA enzyme activity of seasonal H1N1 viruses circulating before and after 2009, as well as viruses with avian or swine N1s. The mAbs provided robust protection from lethal challenge with human H1N1 and avian H5N1 viruses in mice, and both target an epitope on the lateral face of NA. In summary, we identified two broadly protective NA antibodies that share a novel epitope, inhibited NA activity, and provide protection against virus challenge in mice. Our work reaffirms that NA should be included as a target in future broadly protective or universal influenza virus vaccines.

PubMed: 37506693
DOI: 10.1016/j.immuni.2023.07.004

実験手法

ELECTRON MICROSCOPY (2.7 Å)