Small molecule stabilization of non-native protein-protein interactions of SARS-CoV-2 N protein as a mechanism of action against COVID-19

被引:4
作者
Fernandez, Julian F. [1 ,2 ]
Lavecchia, Martin J. [3 ]
机构
[1] Univ Buenos Aires, Fac Ciencias Exactas & Nat, Dept Quim Organ, Buenos Aires, DF, Argentina
[2] Univ Buenos Aires, CONICET, Unidad Microanal & Metodos Fis Quim Organ UMYMFOR, Buenos Aires, DF, Argentina
[3] Univ Nacl La Plata, Fac Ciencias Exactas, Associated CIC PBA, CEQUINOR,UNLP CONICET,CCT La Plata,Dept Quim, Blvd 120 1465, RA-1900 La Plata, Argentina
关键词
Molecular dynamics; docking; coronavirus; virtual screening;
D O I
10.1080/07391102.2020.1860828
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The outbreak of COVID-19, the disease caused by SARS-CoV-2, continues to affect millions of people around the world. The absence of a globally distributed effective treatment makes the exploration of new mechanisms of action a key step to address this situation. Stabilization of non-native Protein-Protein Interactions (PPIs) of the nucleocapsid protein of MERS-CoV has been reported as a valid strategy to inhibit viral replication. In this study, the applicability of this unexplored mechanism of action against SARS-CoV-2 is analyzed. During our research, we were able to find three inducible interfaces of SARS-CoV-2 N protein NTD, compare them to the previously reported MERS-CoV stabilized dimers, and identify those residues that are responsible for their formation. A drug discovery protocol implemented consisting of docking, molecular dynamics and MM-GBSA enabled us to find several compounds that might be able to exploit this mechanism of action. In addition, a common catechin skeleton was found among many of these molecules, which might be useful for further drug design. We consider that our findings could motivate future research in the fields of drug discovery and design towards the exploitation of this previously unexplored mechanism of action against COVID-19. Communicated by Ramaswamy H. Sarma
引用
收藏
页码:4488 / 4495
页数:8
相关论文
共 31 条
[1]   Stabilization of protein-protein interactions in drug discovery [J].
Andrei, Sebastian A. ;
Sijbesma, Eline ;
Hann, Michael ;
Davis, Jeremy ;
O'Mahony, Gavin ;
Perry, Matthew W. D. ;
Karawajczyk, Anna ;
Eickhoff, Jan ;
Brunsveld, Luc ;
Doveston, Richard G. ;
Milroy, Lech-Gustav ;
Ottmann, Christian .
EXPERT OPINION ON DRUG DISCOVERY, 2017, 12 (09) :925-940
[2]  
[Anonymous], Quacpac
[3]  
[Anonymous], 2004, Gaussian03
[4]  
[Anonymous], DATABASE J BIOL DATA
[5]  
BOSC N, 2017, J CHEM INF MODEL, V57
[6]  
Case D., 2019, AMBERTOOLS19
[7]   p15PAF Is an Rb/E2F-Regulated S-Phase Protein Essential for DNA Synthesis and Cell Cycle Progression [J].
Chang, Chih-Ning ;
Feng, Mow-Jung ;
Chen, Yu-Ling ;
Yuan, Ray-Hwang ;
Jeng, Yung-Ming .
PLOS ONE, 2013, 8 (04)
[8]   The SARS coronavirus nucleocapsid protein - Forms and functions [J].
Chang, Chung-ke ;
Hou, Ming-Hon ;
Chang, Chi-Fon ;
Hsiao, Chwan-Deng ;
Huang, Tai-huang .
ANTIVIRAL RESEARCH, 2014, 103 :39-50
[9]   Does zinc supplementation enhance the clinical efficacy of chloroquine/hydroxychloroquine to win today's battle against COVID-19? [J].
Derwand, R. ;
Scholz, M. .
MEDICAL HYPOTHESES, 2020, 142
[10]   A guideline for homology modeling of the proteins from newly discovered betacoronavirus, 2019 novel coronavirus (2019-nCoV) [J].
Dong, Shengjie ;
Sun, Jiachen ;
Mao, Zhuo ;
Wang, Lu ;
Lu, Yi-Lin ;
Li, Jiesen .
JOURNAL OF MEDICAL VIROLOGY, 2020, 92 (09) :1542-1548