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用于黄病毒药物研发的分子靶点。

Molecular targets for flavivirus drug discovery.

作者信息

Sampath Aruna, Padmanabhan R

机构信息

National Center for Natural Product Research, Research Institute of Pharmaceutical Sciences, School of Pharmacy, University of Mississippi, University, MS 38677, USA.

出版信息

Antiviral Res. 2009 Jan;81(1):6-15. doi: 10.1016/j.antiviral.2008.08.004. Epub 2008 Sep 15.

DOI:10.1016/j.antiviral.2008.08.004
PMID:18796313
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2647018/
Abstract

Flaviviruses are a major cause of infectious disease in humans. Dengue virus causes an estimated 50 million cases of febrile illness each year, including an increasing number of cases of hemorrhagic fever. West Nile virus, which recently spread from the Mediterranean basin to the Western Hemisphere, now causes thousands of sporadic cases of encephalitis annually. Despite the existence of licensed vaccines, yellow fever, Japanese encephalitis and tick-borne encephalitis also claim many thousands of victims each year across their vast endemic areas. Antiviral therapy could potentially reduce morbidity and mortality from flavivirus infections, but no effective drugs are currently available. This article introduces a collection of papers in Antiviral Research on molecular targets for flavivirus antiviral drug design and murine models of dengue virus disease that aims to encourage drug development efforts. After reviewing the flavivirus replication cycle, we discuss the envelope glycoprotein, NS3 protease, NS3 helicase, NS5 methyltransferase and NS5 RNA-dependent RNA polymerase as potential drug targets, with special attention being given to the viral protease. The other viral proteins are the subject of individual articles in the journal. Together, these papers highlight current status of drug discovery efforts for flavivirus diseases and suggest promising areas for further research.

摘要

黄病毒是人类传染病的主要病因。登革病毒每年估计导致5000万例发热性疾病,其中出血热病例数不断增加。西尼罗河病毒最近从地中海盆地传播到西半球,现在每年导致数千例散发性脑炎病例。尽管有已获许可的疫苗,但黄热病、日本脑炎和蜱传脑炎每年在其广阔的流行地区也夺去数千人的生命。抗病毒疗法有可能降低黄病毒感染的发病率和死亡率,但目前尚无有效的药物。本文介绍了《抗病毒研究》上发表的一系列论文,这些论文涉及黄病毒抗病毒药物设计的分子靶点以及登革病毒疾病的小鼠模型,旨在鼓励药物研发工作。在回顾了黄病毒复制周期后,我们讨论了包膜糖蛋白、NS3蛋白酶、NS3解旋酶、NS5甲基转移酶和NS5 RNA依赖性RNA聚合酶作为潜在的药物靶点,特别关注了病毒蛋白酶。其他病毒蛋白是该期刊上各篇文章的主题。这些论文共同突出了黄病毒疾病药物研发工作的现状,并指出了有前景的进一步研究领域。

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Molecular targets for flavivirus drug discovery.用于黄病毒药物研发的分子靶点。
Antiviral Res. 2009 Jan;81(1):6-15. doi: 10.1016/j.antiviral.2008.08.004. Epub 2008 Sep 15.
2
Recent advances in flavivirus antiviral drug discovery and vaccine development.黄病毒抗病毒药物研发与疫苗开发的最新进展。
Recent Pat Antiinfect Drug Discov. 2006 Jan;1(1):45-55. doi: 10.2174/157489106775244055.
3
Potential Role of Flavivirus NS2B-NS3 Proteases in Viral Pathogenesis and Anti-flavivirus Drug Discovery Employing Animal Cells and Models: A Review.黄病毒 NS2B-NS3 蛋白酶在病毒发病机制和利用动物细胞及模型的抗黄病毒药物研发中的潜在作用:综述。
Viruses. 2021 Dec 28;14(1):44. doi: 10.3390/v14010044.
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The Many Faces of the Flavivirus NS5 Protein in Antagonism of Type I Interferon Signaling.黄病毒NS5蛋白在拮抗I型干扰素信号传导中的多种作用
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Inhibition of Flaviviruses by Targeting a Conserved Pocket on the Viral Envelope Protein.靶向病毒包膜蛋白保守口袋抑制黄病毒。
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Cellular NONO protein binds to the flavivirus replication complex and promotes positive-strand RNA synthesis.细胞中的 NONO 蛋白与黄病毒复制复合体结合并促进正链 RNA 合成。
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Lipids and flaviviruses, present and future perspectives for the control of dengue, Zika, and West Nile viruses.脂类与黄病毒:登革热、寨卡病毒和西尼罗河病毒防控的现状与未来展望。
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Small-Molecule Inhibitor of Flaviviral NS3-NS5 Interaction with Broad-Spectrum Activity and Efficacy .小分子抑制剂抑制黄病毒 NS3-NS5 相互作用,具有广谱活性和疗效。
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引用本文的文献

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In silico fragment-based design and pharmacophore modelling of therapeutics against dengue virus envelope protein.基于计算机模拟的登革病毒包膜蛋白治疗药物的片段设计与药效团建模
In Silico Pharmacol. 2024 Sep 20;12(2):87. doi: 10.1007/s40203-024-00262-9. eCollection 2024.
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Dengue Fever as a Re-emergent Priority of Public Health; a Letter to Editor.登革热作为公共卫生领域重新出现的优先事项;致编辑的一封信
Arch Acad Emerg Med. 2024 Aug 19;12(1):e62. doi: 10.22037/aaem.v12i1.2268. eCollection 2024.
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Japanese encephalitis virus NS5 protein interacts with nucleolin to enhance the virus replication.

本文引用的文献

1
Towards the design of antiviral inhibitors against flaviviruses: the case for the multifunctional NS3 protein from Dengue virus as a target.针对黄病毒的抗病毒抑制剂设计:以登革病毒多功能NS3蛋白为靶点的案例
Antiviral Res. 2008 Nov;80(2):94-101. doi: 10.1016/j.antiviral.2008.07.001. Epub 2008 Jul 30.
2
Mouse models of dengue virus infection and disease.登革病毒感染与疾病的小鼠模型。
Antiviral Res. 2008 Nov;80(2):87-93. doi: 10.1016/j.antiviral.2008.06.010. Epub 2008 Jul 9.
3
The flavivirus polymerase as a target for drug discovery.
日本脑炎病毒 NS5 蛋白与核仁素相互作用以增强病毒复制。
J Virol. 2024 Aug 20;98(8):e0085824. doi: 10.1128/jvi.00858-24. Epub 2024 Jul 30.
4
Implementation of IFPTML Computational Models in Drug Discovery Against Flaviviridae Family.实施 IFPTML 计算模型在抗黄病毒科药物发现中的应用。
J Chem Inf Model. 2024 Mar 25;64(6):1841-1852. doi: 10.1021/acs.jcim.3c01796. Epub 2024 Mar 11.
5
Japanese encephlu emergence in Australia: the potential population at risk.日本脑炎在澳大利亚的出现:潜在的风险人群。 (注:encephlu应改为encephalitis,可能是拼写错误)
Ann Med Surg (Lond). 2024 Jan 22;86(3):1540-1549. doi: 10.1097/MS9.0000000000001739. eCollection 2024 Mar.
6
Shift in dominant genotypes of Japanese encephalitis virus and its impact on current vaccination strategies.日本脑炎病毒优势基因型的转变及其对当前疫苗接种策略的影响。
Front Microbiol. 2023 Nov 17;14:1302101. doi: 10.3389/fmicb.2023.1302101. eCollection 2023.
7
Structural Modifications Introduced by NS2B Cofactor Binding to the NS3 Protease of the Kyasanur Forest Disease Virus.NS2B 共因子结合到 Kyasanur 森林病病毒 NS3 蛋白酶引起的结构修饰。
Int J Mol Sci. 2023 Jun 30;24(13):10907. doi: 10.3390/ijms241310907.
8
Recent Advances in Antivirals for Japanese Encephalitis Virus.日本脑炎病毒抗病毒药物的最新进展。
Viruses. 2023 Apr 23;15(5):1033. doi: 10.3390/v15051033.
9
Japanese Encephalitis Virus: An Update on the Potential Antivirals and Vaccines.日本脑炎病毒:潜在抗病毒药物和疫苗的最新情况
Vaccines (Basel). 2023 Mar 27;11(4):742. doi: 10.3390/vaccines11040742.
10
Significance of Conserved Regions in Coronavirus Spike Protein for Developing a Novel Vaccine against SARS-CoV-2 Infection.冠状病毒刺突蛋白中保守区域对研发抗SARS-CoV-2感染新型疫苗的意义
Vaccines (Basel). 2023 Feb 24;11(3):545. doi: 10.3390/vaccines11030545.
黄病毒聚合酶作为药物研发的靶点。
Antiviral Res. 2008 Oct;80(1):23-35. doi: 10.1016/j.antiviral.2008.06.007. Epub 2008 Jul 9.
4
Identification and biochemical characterization of small-molecule inhibitors of west nile virus serine protease by a high-throughput screen.通过高通量筛选鉴定西尼罗河病毒丝氨酸蛋白酶的小分子抑制剂并进行生化特性分析。
Antimicrob Agents Chemother. 2008 Sep;52(9):3385-93. doi: 10.1128/AAC.01508-07. Epub 2008 Jul 7.
5
Closing the door on flaviviruses: entry as a target for antiviral drug design.对黄病毒关上大门:将病毒进入作为抗病毒药物设计的靶点
Antiviral Res. 2008 Oct;80(1):11-22. doi: 10.1016/j.antiviral.2008.05.004. Epub 2008 Jun 11.
6
Flavivirus methyltransferase: a novel antiviral target.黄病毒甲基转移酶:一种新型抗病毒靶点。
Antiviral Res. 2008 Oct;80(1):1-10. doi: 10.1016/j.antiviral.2008.05.003. Epub 2008 Jun 5.
7
Hepatitis C protease and polymerase inhibitors in development.正在研发的丙型肝炎蛋白酶和聚合酶抑制剂。
AIDS Patient Care STDS. 2008 Jun;22(6):449-57. doi: 10.1089/apc.2007.0199.
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Genetic interactions among the West Nile virus methyltransferase, the RNA-dependent RNA polymerase, and the 5' stem-loop of genomic RNA.西尼罗河病毒甲基转移酶、RNA 依赖性 RNA 聚合酶与基因组 RNA 的 5' 茎环之间的遗传相互作用。
J Virol. 2008 Jul;82(14):7047-58. doi: 10.1128/JVI.00654-08. Epub 2008 Apr 30.
9
Future directions in therapy for chronic hepatitis C.慢性丙型肝炎治疗的未来方向
Antivir Ther. 2008;13 Suppl 1:31-6.
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Structure of the immature dengue virus at low pH primes proteolytic maturation.低pH值下未成熟登革病毒的结构引发蛋白水解成熟。
Science. 2008 Mar 28;319(5871):1834-7. doi: 10.1126/science.1153264.