Suppr超能文献

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。

相似文献

3
Flavivirus NS4B protein: Structure, function, and antiviral discovery.黄病毒 NS4B 蛋白:结构、功能与抗病毒药物研发。
Antiviral Res. 2022 Nov;207:105423. doi: 10.1016/j.antiviral.2022.105423. Epub 2022 Sep 27.
6
Flavivirus enzymes and their inhibitors.黄病毒酶及其抑制剂。
Enzymes. 2021;49:265-303. doi: 10.1016/bs.enz.2021.07.006. Epub 2021 Sep 1.
7
Establishment and Application of Flavivirus Replicons.黄病毒复制子的建立与应用。
Adv Exp Med Biol. 2018;1062:165-173. doi: 10.1007/978-981-10-8727-1_12.

引用本文的文献

本文引用的文献

4
Investigating the conformational dynamics of Zika virus NS4B protein.研究寨卡病毒 NS4B 蛋白的构象动态。
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.ColabFold:让蛋白质折叠变得人人可用。
Nat Methods. 2022 Jun;19(6):679-682. doi: 10.1038/s41592-022-01488-1. Epub 2022 May 30.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验