Suppr超能文献

一种基于AlphaScreen®的用于高通量筛选核输入特异性抑制剂的检测方法。

An AlphaScreen®-based assay for high-throughput screening for specific inhibitors of nuclear import.

作者信息

Wagstaff Kylie M, Rawlinson Stephen M, Hearps Anna C, Jans David A

机构信息

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

出版信息

J Biomol Screen. 2011 Feb;16(2):192-200. doi: 10.1177/1087057110390360.

Abstract

Specific viral proteins enter the nucleus of infected cells to perform essential functions, as part of the viral life cycle. The integrase (IN) molecule of human immunodeficiency virus (HIV)-1 is of particular interest in this context due to its integral role in integrating the HIV genome into that of the infected host cell. Most IN-based antiviral compounds target the IN/DNA interaction, but since IN must first enter the nucleus before it can perform these critical functions, nuclear transport of IN is also an attractive target for therapeutic intervention. Here the authors describe a novel high-throughput screening assay for identifying inhibitors of nuclear import, particularly IN, based on amplified luminescent proximity homogeneous assay (AlphaScreen(®)) technology, which is high throughput, requires low amounts of material, and is efficient and cost-effective. The authors use the assay to screen for specific inhibitors of the interaction between IN and its nuclear transport receptor importin α/β, successfully identifying several inhibitors of the IN/importin α/β interaction. Importantly, they demonstrate that one of the identified compounds, mifepristone, is effective in preventing active nuclear transport of IN in transfected cells and hence may represent a useful anti-HIV therapeutic. The screen also identified broad-spectrum importin α/β inhibitors such as ivermectin, which may represent useful tools for nuclear transport research in the future. The authors validate the activity and specificity of mifepristone and ivermectin in inhibiting nuclear protein import in living cells, underlining the utility of the screening approach.

摘要

作为病毒生命周期的一部分,特定的病毒蛋白会进入受感染细胞的细胞核以执行基本功能。在这种情况下,人类免疫缺陷病毒1型(HIV-1)的整合酶(IN)分子特别受关注,因为它在将HIV基因组整合到受感染宿主细胞基因组中起着不可或缺的作用。大多数基于整合酶的抗病毒化合物靶向整合酶与DNA的相互作用,但由于整合酶在执行这些关键功能之前必须先进入细胞核,因此整合酶的核运输也是治疗干预的一个有吸引力的靶点。本文作者描述了一种基于放大发光邻近均相分析(AlphaScreen®)技术的新型高通量筛选方法,用于鉴定核输入抑制剂,特别是整合酶的抑制剂,该技术具有高通量、所需材料量少、高效且经济高效的特点。作者使用该方法筛选整合酶与其核运输受体输入蛋白α/β之间相互作用的特异性抑制剂,成功鉴定出几种整合酶/输入蛋白α/β相互作用的抑制剂。重要的是,他们证明所鉴定的化合物之一米非司酮在转染细胞中可有效阻止整合酶的主动核运输,因此可能是一种有用的抗HIV治疗药物。该筛选还鉴定出了如伊维菌素等广谱输入蛋白α/β抑制剂,它们未来可能是核运输研究的有用工具。作者验证了米非司酮和伊维菌素在抑制活细胞中核蛋白输入方面的活性和特异性,强调了该筛选方法的实用性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验