Crucial steps in the structure determination of a coronavirus spike glycoprotein using cryo-electron microscopy

被引:26
|
作者
Walls, Alexandra [1 ]
Tortorici, M. Alejandra [2 ,3 ]
Bosch, Berend-Jan [4 ]
Frenz, Brandon [1 ]
Rottier, Peter J. M. [4 ]
DiMaio, Frank [1 ]
Rey, Felix A. [2 ,3 ]
Veesler, David [1 ]
机构
[1] Univ Washington, Dept Biochem, Seattle, WA 98195 USA
[2] Inst Pasteur, Unite Virol Struct, Dept Virol, Paris, France
[3] CNRS, UMR 3569, Virol, Paris, France
[4] Univ Utrecht, Div Virol, Dept Infect Dis & Immunol, Fac Vet Med, NL-3584 CL Utrecht, Netherlands
基金
美国国家卫生研究院;
关键词
coronavirus spike protein; cryo-electron microscopy; rational vaccine design; rosetta; relion; RESPIRATORY SYNDROME CORONAVIRUS; EM STRUCTURE DETERMINATION; PARTICLE CRYO-EM; CRYSTAL-STRUCTURE; ELECTRON CRYOMICROSCOPY; MEMBRANE-FUSION; NEUTRALIZING ANTIBODY; PROTEIN; RESOLUTION; RECEPTOR;
D O I
10.1002/pro.3048
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 tremendous pandemic potential of coronaviruses was demonstrated twice in the last 15 years by two global outbreaks of deadly pneumonia. Entry of coronaviruses into cells is mediated by the transmembrane spike glycoprotein S, which forms a trimer carrying receptor-binding and membrane fusion functions. Despite their biomedical importance, coronavirus S glycoproteins have proven difficult targets for structural characterization, precluding high-resolution studies of the biologically relevant trimer. Recent technological developments in single particle cryo-electron microscopy allowed us to determine the first structure of a coronavirus S glycoprotein trimer which provided a framework to understand the mechanisms of viral entry and suggested potential inhibition strategies for this family of viruses. Here, we describe the key factors that enabled this breakthrough.
引用
收藏
页码:113 / 121
页数:9
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