Structural Basis of Protection against H7N9 Influenza Virus by Human Anti-N9 Neuraminidase Antibodies

被引:55
作者
Zhu, Xueyong [1 ]
Turner, Hannah L. [1 ]
Lang, Shanshan [1 ]
McBride, Ryan [2 ,3 ]
Bangaru, Sandhya [4 ]
Gilchuk, Iuliia M. [4 ]
Yu, Wenli [1 ]
Paulson, James C. [2 ,3 ]
Crowe, James E., Jr. [4 ,5 ,6 ]
Ward, Andrew B. [1 ]
Wilson, Ian A. [1 ,7 ]
机构
[1] Scripps Res Inst, Dept Integrat Struct & Computat Biol, La Jolla, CA 92037 USA
[2] Scripps Res Inst, Dept Mol Med, La Jolla, CA 92037 USA
[3] Scripps Res Inst, Dept Immunol & Microbiol, La Jolla, CA 92037 USA
[4] Vanderbilt Univ, Vanderbilt Vaccine Ctr, Med Ctr, Nashville, TN 37232 USA
[5] Vanderbilt Univ, Dept Pathol Microbiol & Immunol, Med Ctr, Nashville, TN 37232 USA
[6] Vanderbilt Univ, Med Ctr, Dept Pediat, Nashville, TN 37232 USA
[7] Scripps Res Inst, Skaggs Inst Chem Biol, La Jolla, CA 92037 USA
基金
美国国家卫生研究院;
关键词
COMPUTATIONAL DESIGN; BINDING-SITE; HEMAGGLUTININ; INFECTION; PROTEINS; VALIDATION; MICROSCOPY;
D O I
10.1016/j.chom.2019.10.002
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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.
引用
收藏
页码:729 / +
页数:14
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