GCG inhibits SARS-CoV-2 replication by disrupting the liquid phase condensation of its nucleocapsid protein

Nat Commun. 2021 Apr 9;12(1):2114. doi: 10.1038/s41467-021-22297-8.

Abstract

Lack of detailed knowledge of SARS-CoV-2 infection has been hampering the development of treatments for coronavirus disease 2019 (COVID-19). Here, we report that RNA triggers the liquid-liquid phase separation (LLPS) of the SARS-CoV-2 nucleocapsid protein, N. By analyzing all 29 proteins of SARS-CoV-2, we find that only N is predicted as an LLPS protein. We further confirm the LLPS of N during SARS-CoV-2 infection. Among the 100,849 genome variants of SARS-CoV-2 in the GISAID database, we identify that ~37% (36,941) of the genomes contain a specific trio-nucleotide polymorphism (GGG-to-AAC) in the coding sequence of N, which leads to the amino acid substitutions, R203K/G204R. Interestingly, NR203K/G204R exhibits a higher propensity to undergo LLPS and a greater effect on IFN inhibition. By screening the chemicals known to interfere with N-RNA binding in other viruses, we find that (-)-gallocatechin gallate (GCG), a polyphenol from green tea, disrupts the LLPS of N and inhibits SARS-CoV-2 replication. Thus, our study reveals that targeting N-RNA condensation with GCG could be a potential treatment for COVID-19.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Substitution / drug effects*
  • COVID-19 / prevention & control*
  • COVID-19 / virology
  • Catechin / analogs & derivatives*
  • Catechin / pharmacology
  • Genome, Viral / genetics
  • Humans
  • Liquid-Liquid Extraction
  • Nucleocapsid Proteins / genetics*
  • Nucleocapsid Proteins / metabolism
  • RNA, Viral / genetics
  • RNA, Viral / metabolism
  • SARS-CoV-2 / drug effects*
  • SARS-CoV-2 / genetics
  • Virus Replication / drug effects*
  • Virus Replication / genetics

Substances

  • Nucleocapsid Proteins
  • RNA, Viral
  • gallocatechin gallate
  • Catechin