Integrative structural studies of the SARS-CoV-2 spike protein during the fusion process (2022)

被引:1
作者
Miner, Jacob C. [1 ]
Fenimore, Paul W. [1 ]
Fischer, William M. [1 ]
McMahon, Benjamin H. [1 ]
Sanbonmatsu, Karissa Y. [1 ,2 ]
Tung, Chang-Shung [1 ]
机构
[1] Alamos Natl Lab, Theoret Div, Theoret Biol & Biophys Grp, Los Alamos, NM 87545 USA
[2] New Mexico Consortium, Los Alamos, NM 87544 USA
来源
CURRENT RESEARCH IN STRUCTURAL BIOLOGY | 2022年 / 4卷
关键词
MERS-COV; INFLUENZA HEMAGGLUTININ; CRYSTAL-STRUCTURE; COILED-COILS; CELL ENTRY; CORONAVIRUS; BINDING; CLEAVAGE; TRANSLOCATION; GLYCOPROTEIN;
D O I
10.1016/j.crstbi.2022.06.004
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
SARS-CoV-2 is the virus responsible for the COVID-19 pandemic and catastrophic, worldwide health and eco-nomic impacts. The spike protein on the viral surface is responsible for viral entry into the host cell. The binding of spike protein to the host cell receptor ACE2 is the first step leading to fusion of the host and viral membranes. Despite the vast amount of structure data that has been generated for the spike protein of SARS-CoV-2, many of the detailed structures of the spike protein in different stages of the fusion pathway are unknown, leaving a wealth of potential drug-target space unexplored. The atomic-scale structure of the complete S2 segment, as well as the complete fusion intermediate are also unknown and represent major gaps in our knowledge of the infectious pathway of SAR-CoV-2. The conformational changes of the spike protein during this process are similarly not well understood. Here we present structures of the spike protein at different stages of the fusion process. With the transitions being a necessary step before the receptor binding, we propose sites along the transition pathways as potential targets for drug development.
引用
收藏
页码:220 / 230
页数:11
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