Cryptococcal Protease(s) and the Activation of SARS-CoV-2 Spike (S) Protein

Cells. 2022 Jan 27;11(3):437. doi: 10.3390/cells11030437.

Abstract

In this contribution, we report on the possibility that cryptococcal protease(s) could activate the SARS-CoV-2 spike (S) protein. The S protein is documented to have a unique four-amino-acid sequence (underlined, SPRRAR↓S) at the interface between the S1 and S2 sites, that serves as a cleavage site for the human protease, furin. We compared the biochemical efficiency of cryptococcal protease(s) and furin to mediate the proteolytic cleavage of the S1/S2 site in a fluorogenic peptide. We show that cryptococcal protease(s) processes this site in a manner comparable to the efficiency of furin (p > 0.581). We conclude the paper by discussing the impact of these findings in the context of a SARS-CoV-2 disease manifesting while there is an underlying cryptococcal infection.

Keywords: Cryptococcus; Cryptococcus neoformans; S1/S2 cleavage site; SARS-CoV-2; cryptococcal infection; fluorogenic peptide; furin; protease; proteolytic cleavage; spike (S) protein.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Aspartic Acid Proteases / genetics
  • Aspartic Acid Proteases / metabolism*
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism*
  • Binding Sites
  • COVID-19 / epidemiology
  • COVID-19 / prevention & control
  • COVID-19 / virology
  • Cryptococcus neoformans / enzymology*
  • Cryptococcus neoformans / genetics
  • Fluorescent Dyes / chemistry
  • Furin / genetics
  • Furin / metabolism
  • Humans
  • Pandemics
  • Peptides / chemistry
  • Peptides / metabolism
  • Proteolysis
  • SARS-CoV-2 / metabolism*
  • SARS-CoV-2 / physiology
  • Spike Glycoprotein, Coronavirus / metabolism*

Substances

  • Bacterial Proteins
  • Fluorescent Dyes
  • Peptides
  • Spike Glycoprotein, Coronavirus
  • spike protein, SARS-CoV-2
  • Aspartic Acid Proteases
  • Furin