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研究登革病毒非结构蛋白5(NS5)的核输入。

Investigating dengue virus nonstructural protein 5 (NS5) nuclear import.

作者信息

Fraser Johanna E, Rawlinson Stephen M, Wang Chunxiao, Jans David A, Wagstaff Kylie M

机构信息

Department of Biochemistry and Molecular Biology, Nuclear Signaling Laboratory, Monash University, Clayton, Australia.

出版信息

Methods Mol Biol. 2014;1138:301-28. doi: 10.1007/978-1-4939-0348-1_19.

Abstract

Dengue virus (DENV) nonstructural protein 5 (NS5) plays a central role in viral replication in the cytoplasm of infected cells. Despite this, NS5 is predominantly located in the nucleus of infected cells where it is thought to play a role in suppression of the host antiviral response. We have investigated the nuclear localization of NS5 using immunofluorescent staining for NS5 in infected cells, showing that NS5 nuclear localization is significantly inhibited by Ivermectin, a general inhibitor of nuclear transport mediated by the cellular nuclear transport proteins importin α/β (IMPα/β). Experiments in living mammalian cells transfected to express green fluorescent protein (GFP)-tagged NS5 protein confirm that NS5 is predominantly nuclear and that this localization is inhibited by Ivermectin, demonstrating that NS5 contains an Ivermectin-sensitive IMPα/β-recognized nuclear localization signal [Pryor et al. Traffic 8:795-807, 2007]. Consistent with this observation, mutation of critical residues within the nuclear localization signal (the A2 mutant; [Pryor et al. Traffic 8:795-807, 2007]) results in an 80 % reduction in nuclear localization of NS5. Finally we demonstrate direct, high-affinity binding of NS5 to IMPα/β using an AlphaScreen protein-protein binding assay.

摘要

登革病毒(DENV)非结构蛋白5(NS5)在受感染细胞的细胞质中病毒复制过程中发挥核心作用。尽管如此,NS5主要位于受感染细胞的细胞核中,据认为它在抑制宿主抗病毒反应中发挥作用。我们利用对受感染细胞中NS5进行免疫荧光染色的方法研究了NS5的核定位,结果显示,伊维菌素(一种由细胞核转运蛋白输入蛋白α/β(IMPα/β)介导的核转运的通用抑制剂)可显著抑制NS5的核定位。在转染以表达绿色荧光蛋白(GFP)标记的NS5蛋白的活哺乳动物细胞中进行的实验证实,NS5主要定位于细胞核,且这种定位受伊维菌素抑制,这表明NS5含有一个伊维菌素敏感的、IMPα/β识别的核定位信号[Pryor等人,《Traffic》8:795 - 807,2007年]。与这一观察结果一致,核定位信号内关键残基的突变(A2突变体;[Pryor等人,《Traffic》8:795 - 807,2007年])导致NS5的核定位减少80%。最后,我们使用AlphaScreen蛋白质 - 蛋白质结合测定法证明了NS5与IMPα/β之间存在直接的高亲和力结合。

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