Mechanisms of Coronavirus Cell Entry Mediated by the Viral Spike Protein

Mechanisms of Coronavirus Cell Entry Mediated by the Viral Spike Protein

Gary R. Whittaker, Beth N. Licitra, Sandrine Belouzard, Jean K. Millet

Coronaviruses are enveloped positive-stranded RNA viruses that replicate in the cytoplasm. To deliver their nucleocapsid into the host cell, they rely on the fusion of their envelope with the host cell membrane. The spike glycoprotein (S) mediates virus entry and is a primary determinant of cell tropism and pathogenesis. It is classified as a class I fusion protein, and is responsible for binding to the receptor on the host cell as well as mediating the fusion of host and viral membranes—A process driven by major conformational changes of the S protein. This review discusses coronavirus entry mechanisms focusing on the different triggers used by coronaviruses to initiate the conformational change of the S protein: receptor binding, low pH exposure and proteolytic activation. We also highlight commonalities between coronavirus S proteins and other class I viral fusion proteins, as well as distinctive features that confer distinct tropism, pathogenicity and host interspecies transmission characteristics to coronaviruses.

2012

coronavirus, Spike, viral entry, Fusion, proteolytic activation

DOI: 10.3390/v4061011

Viruses

MDPI AG

Microbiology

EN