• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

由寨卡病毒 RNA 聚合酶结构域催化的从头 RNA 合成。

De novo RNA synthesis catalyzed by the Zika Virus RNA polymerase domain.

机构信息

Univ. Bordeaux, CNRS, MFP, UMR 5234, 146 rue Léo Saignat, Bordeaux cedex, 33076, France.

Fédération de Recherche "TransbioMed", Bordeaux, France.

出版信息

Sci Rep. 2017 Jun 2;7(1):2697. doi: 10.1038/s41598-017-03038-8.

DOI:10.1038/s41598-017-03038-8
PMID:28577343
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5457451/
Abstract

Mosquito- and tick-borne pathogens including Chikungunya, Dengue, Japanese encephalitis, West Nile, Yellow fever and Zika virus, represent a new economic and public health challenge. In the absence of effective vaccines and specific therapies, only supportive regimens are administrated for most of these infections. Thus, the development of a targeted therapy is mandatory to stop the rapid progression of these pathogens and preoccupant associated burdens such as Guillain-Barre syndrome, microcephaly. For this, it is essential to develop biochemical tools to help study and target key viral enzymes involved in replication such as helicase complexes, methyl-transferases and RNA-dependent RNA polymerases. Here, we show that a highly purified ZIKV polymerase domain is active in vitro. Importantly, we show that this isolated domain is capable of de novo synthesis of the viral genome and efficient elongation without terminal nucleotide transferase activity. Altogether, this isolated polymerase domain will be a precious tool to screen and optimize specific nucleoside and non-nucleoside inhibitors to fight against Zika infections.

摘要

蚊媒和蜱媒病原体包括基孔肯雅热、登革热、日本脑炎、西尼罗河热、黄热病和寨卡病毒,它们给经济和公共卫生带来了新的挑战。由于缺乏有效的疫苗和特效疗法,对于大多数此类感染,仅能提供支持性治疗方案。因此,必须开发靶向疗法来阻止这些病原体的快速传播,并解决与吉兰-巴雷综合征、小头畸形等相关的负担。为此,开发生化工具来帮助研究和针对参与复制的关键病毒酶(如解旋酶复合物、甲基转移酶和 RNA 依赖性 RNA 聚合酶)至关重要。在这里,我们证明了高度纯化的寨卡病毒聚合酶结构域在体外具有活性。重要的是,我们表明这个分离的结构域能够从头合成病毒基因组并进行有效的延伸,而没有末端核苷酸转移酶活性。总之,这个分离的聚合酶结构域将成为筛选和优化针对寨卡病毒感染的特定核苷和非核苷抑制剂的宝贵工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5151/5457451/c862e0c09b0c/41598_2017_3038_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5151/5457451/922e4a7d4d46/41598_2017_3038_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5151/5457451/b64b666d277e/41598_2017_3038_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5151/5457451/531af413beac/41598_2017_3038_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5151/5457451/c862e0c09b0c/41598_2017_3038_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5151/5457451/922e4a7d4d46/41598_2017_3038_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5151/5457451/b64b666d277e/41598_2017_3038_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5151/5457451/531af413beac/41598_2017_3038_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5151/5457451/c862e0c09b0c/41598_2017_3038_Fig4_HTML.jpg

相似文献

1
De novo RNA synthesis catalyzed by the Zika Virus RNA polymerase domain.由寨卡病毒 RNA 聚合酶结构域催化的从头 RNA 合成。
Sci Rep. 2017 Jun 2;7(1):2697. doi: 10.1038/s41598-017-03038-8.
2
Functional RNA during Zika virus infection.寨卡病毒感染期间的功能性 RNA。
Virus Res. 2018 Aug 2;254:41-53. doi: 10.1016/j.virusres.2017.08.015. Epub 2017 Aug 31.
3
Purification of Zika virus RNA-dependent RNA polymerase and its use to identify small-molecule Zika inhibitors.寨卡病毒RNA依赖性RNA聚合酶的纯化及其在鉴定寨卡小分子抑制剂中的应用。
J Antimicrob Chemother. 2017 Mar 1;72(3):727-734. doi: 10.1093/jac/dkw514.
4
Analysis of Ribonucleotide 5'-Triphosphate Analogs as Potential Inhibitors of Zika Virus RNA-Dependent RNA Polymerase by Using Nonradioactive Polymerase Assays.通过非放射性聚合酶测定法分析核糖核苷酸5'-三磷酸类似物作为寨卡病毒RNA依赖性RNA聚合酶的潜在抑制剂
Antimicrob Agents Chemother. 2017 Feb 23;61(3). doi: 10.1128/AAC.01967-16. Print 2017 Mar.
5
RNA-dependent RNA polymerase: Addressing Zika outbreak by a phylogeny-based drug target study.依赖 RNA 的 RNA 聚合酶:基于系统发育的药物靶点研究应对寨卡疫情。
Chem Biol Drug Des. 2018 Jan;91(1):322-327. doi: 10.1111/cbdd.13054. Epub 2017 Jul 29.
6
Zika virus: An emerging flavivirus.寨卡病毒:一种新出现的黄病毒。
J Microbiol. 2017 Mar;55(3):204-219. doi: 10.1007/s12275-017-7063-6. Epub 2017 Feb 28.
7
Discovery of a non-nucleoside RNA polymerase inhibitor for blocking Zika virus replication through in silico screening.通过计算机筛选发现一种非核苷 RNA 聚合酶抑制剂,可阻断寨卡病毒复制。
Antiviral Res. 2018 Mar;151:78-86. doi: 10.1016/j.antiviral.2017.12.016. Epub 2017 Dec 21.
8
Structure and function of the Zika virus full-length NS5 protein.寨卡病毒全长 NS5 蛋白的结构与功能。
Nat Commun. 2017 Mar 27;8:14762. doi: 10.1038/ncomms14762.
9
A Mutation Identified in Neonatal Microcephaly Destabilizes Zika Virus NS1 Assembly in Vitro.一种在新生儿小头畸形中发现的突变使寨卡病毒 NS1 在体外组装不稳定。
Sci Rep. 2017 Feb 15;7:42580. doi: 10.1038/srep42580.
10
Zika virus and the current outbreak: an overview.寨卡病毒与当前疫情概述
Neth J Med. 2016 Mar;74(3):104-9.

引用本文的文献

1
Development of a fluorescence-based method for the rapid determination of Zika virus polymerase activity and the screening of antiviral drugs.建立一种基于荧光的方法,用于快速测定寨卡病毒聚合酶的活性和筛选抗病毒药物。
Sci Rep. 2019 Apr 1;9(1):5397. doi: 10.1038/s41598-019-41998-1.
2
Identification of a Small Interface between the Methyltransferase and RNA Polymerase of NS5 that is Essential for Zika Virus Replication.鉴定 NS5 甲基转移酶和 RNA 聚合酶之间的一个小界面,该界面对于寨卡病毒复制是必需的。
Sci Rep. 2018 Nov 26;8(1):17384. doi: 10.1038/s41598-018-35511-3.

本文引用的文献

1
The clinically approved antiviral drug sofosbuvir inhibits Zika virus replication.临床批准的抗病毒药物索非布韦抑制寨卡病毒复制。
Sci Rep. 2017 Jan 18;7:40920. doi: 10.1038/srep40920.
2
Purification of Zika virus RNA-dependent RNA polymerase and its use to identify small-molecule Zika inhibitors.寨卡病毒RNA依赖性RNA聚合酶的纯化及其在鉴定寨卡小分子抑制剂中的应用。
J Antimicrob Chemother. 2017 Mar 1;72(3):727-734. doi: 10.1093/jac/dkw514.
3
Substrate selectivity of Dengue and Zika virus NS5 polymerase towards 2'-modified nucleotide analogues.
登革热病毒和寨卡病毒NS5聚合酶对2'-修饰核苷酸类似物的底物选择性
Antiviral Res. 2017 Apr;140:25-36. doi: 10.1016/j.antiviral.2016.12.021. Epub 2016 Dec 30.
4
Analysis of Ribonucleotide 5'-Triphosphate Analogs as Potential Inhibitors of Zika Virus RNA-Dependent RNA Polymerase by Using Nonradioactive Polymerase Assays.通过非放射性聚合酶测定法分析核糖核苷酸5'-三磷酸类似物作为寨卡病毒RNA依赖性RNA聚合酶的潜在抑制剂
Antimicrob Agents Chemother. 2017 Feb 23;61(3). doi: 10.1128/AAC.01967-16. Print 2017 Mar.
5
Crystal structure of unlinked NS2B-NS3 protease from Zika virus.寨卡病毒非连接型 NS2B-NS3 蛋白酶的晶体结构。
Science. 2016 Dec 23;354(6319):1597-1600. doi: 10.1126/science.aai9309. Epub 2016 Dec 8.
6
Zika virus produces noncoding RNAs using a multi-pseudoknot structure that confounds a cellular exonuclease.寨卡病毒利用一种能使细胞外切核酸酶失效的多假结结构来产生非编码RNA。
Science. 2016 Dec 2;354(6316):1148-1152. doi: 10.1126/science.aah3963. Epub 2016 Nov 10.
7
The FDA-approved drug sofosbuvir inhibits Zika virus infection.美国食品药品监督管理局(FDA)批准的药物索非布韦可抑制寨卡病毒感染。
Antiviral Res. 2017 Jan;137:134-140. doi: 10.1016/j.antiviral.2016.11.023. Epub 2016 Nov 27.
8
Adenosine triphosphate analogs can efficiently inhibit the Zika virus RNA-dependent RNA polymerase.三磷酸腺苷类似物可有效抑制寨卡病毒的RNA依赖性RNA聚合酶。
Antiviral Res. 2017 Jan;137:131-133. doi: 10.1016/j.antiviral.2016.11.020. Epub 2016 Nov 27.
9
Zika Virus-Associated Micrencephaly: A Thorough Description of Neuropathologic Findings in the Fetal Central Nervous System.寨卡病毒相关小头畸形:胎儿中枢神经系统神经病理学发现的详尽描述
Arch Pathol Lab Med. 2017 Jan;141(1):73-81. doi: 10.5858/arpa.2016-0341-SA. Epub 2016 Oct 11.
10
Structures of NS5 Methyltransferase from Zika Virus.寨卡病毒NS5甲基转移酶的结构
Cell Rep. 2016 Sep 20;16(12):3097-3102. doi: 10.1016/j.celrep.2016.08.091. Epub 2016 Sep 12.