6PZH

Crystal structure of human NA-22 Fab

6PZH の概要

• エントリーDOI: 10.2210/pdb6pzh/pdb
• 分子名称: NA-22 Fab light chain, NA-22 Fab heavy chain (3 entities in total)
• 機能のキーワード: antibody, inhibition mechanism, 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: 96415.09

構造登録者

Zhu, X.,Wilson, I.A. (登録日: 2019-07-31, 公開日: 2019-12-04, 最終更新日: 2024-11-20)

主引用文献

Zhu, X.,Turner, H.L.,Lang, S.,McBride, R.,Bangaru, S.,Gilchuk, I.M.,Yu, W.,Paulson, J.C.,Crowe Jr., J.E.,Ward, A.B.,Wilson, I.A.
Structural Basis of Protection against H7N9 Influenza Virus by Human Anti-N9 Neuraminidase Antibodies.
Cell Host Microbe, 26:729-, 2019

PubMed Abstract: Influenza virus neuraminidase (NA) is a major target for small-molecule antiviral drugs. Antibodies targeting the NA surface antigen could also inhibit virus entry and egress to provide host protection. However, our understanding of the nature and range of target epitopes is limited because of a lack of human antibody structures with influenza neuraminidase. Here, we describe crystal and cryogenic electron microscopy (cryo-EM) structures of NAs from human-infecting avian H7N9 viruses in complex with five human anti-N9 antibodies, systematically defining several antigenic sites and antibody epitope footprints. These antibodies either fully or partially block the NA active site or bind to epitopes distant from the active site while still showing neuraminidase inhibition. The inhibition of antibodies to NAs was further analyzed by glycan array and solution-based NA activity assays. Together, these structural studies provide insights into protection by anti-NA antibodies and templates for the development of NA-based influenza virus vaccines and therapeutics.

PubMed: 31757767
DOI: 10.1016/j.chom.2019.10.002

実験手法

X-RAY DIFFRACTION (2.3 Å)