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黄病毒非结构蛋白和复制复合物作为抗病毒药物靶点。

Flavivirus nonstructural proteins and replication complexes as antiviral drug targets.

机构信息

Lee Kong Chian School of Medicine, Nanyang Technological University, EMB 03-07, 59 Nanyang Drive, Singapore 636921, Singapore; NTU Institute of Structural Biology, Nanyang Technological University, EMB 06-01, 59 Nanyang Drive, Singapore 636921, Singapore; Living Systems Institute, University of Exeter, Exeter EX4 4QD, UK.

Lee Kong Chian School of Medicine, Nanyang Technological University, EMB 03-07, 59 Nanyang Drive, Singapore 636921, Singapore; NTU Institute of Structural Biology, Nanyang Technological University, EMB 06-01, 59 Nanyang Drive, Singapore 636921, Singapore.

出版信息

Curr Opin Virol. 2023 Apr;59:101305. doi: 10.1016/j.coviro.2023.101305. Epub 2023 Mar 2.

Abstract

Many flaviviruses are well-known pathogens, such as dengue, Zika, Japanese encephalitis, and yellow fever viruses. Among them, dengue viruses cause global epidemics and threaten billions of people. Effective vaccines and antivirals are in desperate need. In this review, we focus on the recent advances in understanding viral nonstructural (NS) proteins as antiviral drug targets. We briefly summarize the experimental structures and predicted models of flaviviral NS proteins and their functions. We highlight a few well-characterized inhibitors targeting these NS proteins and provide an update about the latest development. NS4B emerges as one of the most promising drug targets as novel inhibitors targeting NS4B and its interaction network are entering clinical studies. Studies aiming to elucidate the architecture and molecular basis of viral replication will offer new opportunities for novel antiviral discovery. Direct-acting agents against dengue and other pathogenic flaviviruses may be available very soon.

摘要

许多黄病毒都是众所周知的病原体,例如登革热、寨卡、日本脑炎和黄热病病毒。其中,登革热病毒会引起全球流行,威胁着数十亿人的生命。目前急需有效的疫苗和抗病毒药物。在这篇综述中,我们重点介绍了近年来在理解病毒非结构 (NS) 蛋白作为抗病毒药物靶点方面的最新进展。我们简要总结了黄病毒 NS 蛋白的实验结构和预测模型及其功能。我们重点介绍了几种针对这些 NS 蛋白的已充分表征的抑制剂,并提供了最新进展的更新。NS4B 作为最有前途的药物靶点之一脱颖而出,因为针对 NS4B 及其相互作用网络的新型抑制剂已进入临床研究阶段。旨在阐明病毒复制结构和分子基础的研究将为新型抗病毒药物的发现提供新的机会。针对登革热和其他致病性黄病毒的直接作用药物可能很快就会问世。

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Nat Commun. 2022 Nov 9;13(1):6756. doi: 10.1038/s41467-022-34415-1.
3
Molecular Determinants of Tissue Specificity of Flavivirus Nonstructural Protein 1 Interaction with Endothelial Cells.
J Virol. 2022 Oct 12;96(19):e0066122. doi: 10.1128/jvi.00661-22. Epub 2022 Sep 15.
4
Investigating the conformational dynamics of Zika virus NS4B protein.
Virology. 2022 Oct;575:20-35. doi: 10.1016/j.virol.2022.08.005. Epub 2022 Aug 21.
5
ColabFold: making protein folding accessible to all.
Nat Methods. 2022 Jun;19(6):679-682. doi: 10.1038/s41592-022-01488-1. Epub 2022 May 30.
6
Dengue virus NS1 protein conveys pro-inflammatory signals by docking onto high-density lipoproteins.
EMBO Rep. 2022 Jul 5;23(7):e53600. doi: 10.15252/embr.202153600. Epub 2022 May 24.
7
Structure-Based Optimization and Characterization of Macrocyclic Zika Virus NS2B-NS3 Protease Inhibitors.
J Med Chem. 2022 May 12;65(9):6555-6572. doi: 10.1021/acs.jmedchem.1c01860. Epub 2022 Apr 27.
9
Dengue Virus NS1 Uses Scavenger Receptor B1 as a Cell Receptor in Cultured Cells.
J Virol. 2022 Mar 9;96(5):e0166421. doi: 10.1128/JVI.01664-21. Epub 2022 Jan 5.
10
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