Molecular mechanism of resveratrol inhibition of Zika virus NS3 helicase: behind the scenes

被引:4
作者
Devnarain, Nikita [1 ]
Soliman, Mahmoud E. S. [1 ]
机构
[1] Univ KwaZulu Natal, Sch Hlth Sci, Mol Biocomputat & Drug Design Lab, ZA-4001 Durban, South Africa
基金
新加坡国家研究基金会;
关键词
antiviral therapy; flavivirus; molecular dynamics; NS3; helicase; resveratrol; Zika virus; STRUCTURAL FEATURES; NS2B-NS3; PROTEASE; CRYSTAL-STRUCTURE; SIMULATIONS; DOCKING; AMBER; BINDING;
D O I
10.2217/fvl-2018-0170
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Aim: Zika virus (ZIKV) still poses a health risk to women and their babies without US FDA-approved vaccines or treatments. Experimentation has proved resveratrol inhibition of ZIKV NS3 helicase without specifying the molecular events during inhibition. Materials & methods: Herein, we leaped forward to study the molecular dynamics of the bound and unbound enzyme, identifying precise binding residues and interactions, and the enzyme's adaptation to support binding, since loop dynamics affect viral RNA replication. Results: Resveratrol stabilizes the P-loop and causes the RNA-binding loop to block the RNA-binding pocket for 200ns, which is concurrent with experimental evidence that resveratrol binding significantly reduces ATP hydrolysis activity. Conclusion: This study illuminates the structural dynamics of ZIKV helicase and druglikeness of resveratrol, which will advance anti-ZIKV drug development.
引用
收藏
页码:73 / 84
页数:12
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