Ready, Set, Fuse! The Coronavirus Spike Protein and Acquisition of Fusion Competence

被引：252

作者：

Heald-Sargent, Taylor ^{[1
]}

Gallagher, Tom ^{[1
]}

机构：

[1] Loyola Univ, Med Ctr, Dept Microbiol & Immunol, Maywood, IL 60153 USA

来源：

VIRUSES-BASEL | 2012年 / 4卷 / 04期

关键词：

coronavirus; virus entry; viral pathogenesis; spike protein; carcinoembryonic antigen; angiotensin converting enzyme 2; endocytosis; cathepsin; transmembrane protease; membrane fusion; ACUTE RESPIRATORY SYNDROME; TRANSMISSIBLE GASTROENTERITIS CORONAVIRUS; HEPTAD-REPEAT REGIONS; INDUCED CELL-FUSION; TRANSMEMBRANE SERINE PROTEASES; INFECTIOUS-BRONCHITIS VIRUS; PROTEOLYTIC CLEAVAGE SITE; SYNDROME SARS CORONAVIRUS; EXTENDED HOST-RANGE; AMINO-ACID CHANGES;

D O I：

10.3390/v4040557

中图分类号：

Q93 [微生物学];

学科分类号：

071005 ; 100705 ;

摘要：

Coronavirus-cell entry programs involve virus-cell membrane fusions mediated by viral spike (S) proteins. Coronavirus S proteins acquire membrane fusion competence by receptor interactions, proteolysis, and acidification in endosomes. This review describes our current understanding of the S proteins, their interactions with and their responses to these entry triggers. We focus on receptors and proteases in prompting entry and highlight the type II transmembrane serine proteases (TTSPs) known to activate several virus fusion proteins. These and other proteases are essential cofactors permitting coronavirus infection, conceivably being in proximity to cell-surface receptors and thus poised to split entering spike proteins into the fragments that refold to mediate membrane fusion. The review concludes by noting how understanding of coronavirus entry informs antiviral therapies.

引用

页码：557 / 580

页数：24

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