Cryomicroscopy provides structural snapshots of influenza virus membrane fusion

被引:69
|
作者
Calder, Lesley J. [1 ]
Rosenthal, Peter B. [1 ]
机构
[1] Francis Crick Inst, Mill Hill Lab, London, England
基金
英国医学研究理事会; 英国惠康基金;
关键词
A VIRUS; ELECTRON-MICROSCOPY; LOW-PH; CRYOELECTRON TOMOGRAPHY; CONFORMATIONAL-CHANGE; M2; PROTEIN; HEMAGGLUTININ; ARCHITECTURE; COMPLEXES; VIRION;
D O I
10.1038/nsmb.3271
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The lipid-enveloped influenza virus enters host cells during infection by binding cell-surface receptors and, after receptor-mediated endocytosis, fusing with the membrane of the endosome and delivering the viral genome and transcription machinery into the host cell. These events are mediated by the hemagglutinin (HA) surface glycoprotein. At the low pH of the endosome, an irreversible conformational change in the HA, including the exposure of the hydrophobic fusion peptide, activates membrane fusion. Here we used electron cryomicroscopy and cryotomography to image the fusion of influenza virus with target membranes at low pH. We visualized structural intermediates of HA and their interactions with membranes during the course of membrane fusion as well as ultrastructural changes in the virus that accompany membrane fusion. Our observations are relevant to a wide range of protein mediated membrane-fusion processes and demonstrate how dynamic membrane events may be studied by cryomicroscopy.
引用
收藏
页码:853 / 858
页数:6
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