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.

Coronavirus nucleocapsid (N) protein is important for viral genome packaging and virion assembly. Here the authors show that natural chemical (-)-gallocatechin gallate (GCG) disrupts the liquid–liquid phase separation of N and inhibits SARS-CoV-2 replication.

Details

Title
GCG inhibits SARS-CoV-2 replication by disrupting the liquid phase condensation of its nucleocapsid protein
Author
Zhao, Ming 1   VIAFID ORCID Logo  ; Yu, Yu 2   VIAFID ORCID Logo  ; Li-Ming, Sun 3   VIAFID ORCID Logo  ; Jia-Qing, Xing 3 ; Li, Tingting 3 ; Zhu Yunkai 4 ; Wang, Miao 3 ; Yin, Yu 4 ; Xue Wen 3 ; Tian, Xia 3 ; Cai, Hong 3 ; Qiu-Ying, Han 3 ; Yin Xiaoyao 3 ; Wei-Hua, Li 3 ; Ai-Ling, Li 3 ; Cui Jiuwei 5 ; Yuan Zhenghong 4   VIAFID ORCID Logo  ; Zhang, Rong 4   VIAFID ORCID Logo  ; Zhou, Tao 6   VIAFID ORCID Logo  ; Xue-Min, Zhang 7   VIAFID ORCID Logo  ; Li, Tao 7   VIAFID ORCID Logo 

 National Center of Biomedical Analysis, State Key Laboratory of Proteomics, Beijing, China (GRID:grid.410601.2) (ISNI:0000 0004 0427 6573); Nanhu Laboratory, Jiaxing, China (GRID:grid.410601.2) 
 National Center of Biomedical Analysis, State Key Laboratory of Proteomics, Beijing, China (GRID:grid.410601.2) (ISNI:0000 0004 0427 6573); The First Hospital of Jilin University, Cancer Research Institute of Jilin University, Changchun, China (GRID:grid.430605.4) 
 National Center of Biomedical Analysis, State Key Laboratory of Proteomics, Beijing, China (GRID:grid.410601.2) (ISNI:0000 0004 0427 6573) 
 Fudan University, School of Basic Medical Sciences, Shanghai, China (GRID:grid.8547.e) (ISNI:0000 0001 0125 2443) 
 The First Hospital of Jilin University, Cancer Research Institute of Jilin University, Changchun, China (GRID:grid.430605.4) 
 Nanhu Laboratory, Jiaxing, China (GRID:grid.8547.e) 
 National Center of Biomedical Analysis, State Key Laboratory of Proteomics, Beijing, China (GRID:grid.410601.2) (ISNI:0000 0004 0427 6573); Fudan University, School of Basic Medical Sciences, Shanghai, China (GRID:grid.8547.e) (ISNI:0000 0001 0125 2443) 
Publication year
2021
Publication date
2021
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2510491891
Copyright
© The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.