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基于复制子细胞系的高通量抗寨卡病毒药物筛选方法的建立。

Development of a replicon cell line-based high throughput antiviral assay for screening inhibitors of Zika virus.

机构信息

Key Laboratory of Special Pathogens and Biosafety, Wuhan Institute of Virology, Chinese Academy of Science, Wuhan 430071, China; University of Chinese Academy of Sciences, Beijing 100049, China.

Key Laboratory of Special Pathogens and Biosafety, Wuhan Institute of Virology, Chinese Academy of Science, Wuhan 430071, China.

出版信息

Antiviral Res. 2018 Feb;150:148-154. doi: 10.1016/j.antiviral.2017.12.017. Epub 2017 Dec 27.

Abstract

Zika virus (ZIKV) is an important emerging human pathogen associated with microcephaly, Guillain-Barré syndrome and meningoencephalitis. Developing rapid and reliable HTS assay is important for ZIKV drug discovery. Here, we constructed a dicistronic ZIKV replicon (ZIKV-Pac-Rluc-Rep) that contained the Renilla luciferase (Rluc) reporter gene separated from the puromycin N-acetyl-transferase (Pac) selectable marker by a short peptide cleavage site. A clonal replicon cell line stably expressing high level of ZIKV replicon was established by selection with puromycin. By optimizing cell number, compound concentration and incubation time, a robust replicon cell-based HTS assay was developed with a calculated Z' value of >0.5. The fully optimized assay was further validated using several known flavivirus replication inhibitors. Altogether, the replicon cell-based HTS assay developed in this study will facilitate the discovery of antiviral compounds against ZIKV.

摘要

寨卡病毒(ZIKV)是一种重要的新兴人类病原体,与小头畸形、格林-巴利综合征和脑膜脑炎有关。开发快速可靠的高通量筛选(HTS)测定法对于寨卡病毒药物发现很重要。本研究构建了一种包含海肾荧光素酶(Rluc)报告基因的双顺反子寨卡病毒复制子(ZIKV-Pac-Rluc-Rep),该报告基因通过短肽切割位点与嘌呤霉素 N-乙酰转移酶(Pac)选择标记基因分开。通过嘌呤霉素选择,建立了稳定表达高水平寨卡病毒复制子的克隆复制子细胞系。通过优化细胞数量、化合物浓度和孵育时间,建立了一种稳健的基于复制子细胞的 HTS 测定法,其 Z' 值>0.5。使用几种已知的黄病毒复制抑制剂进一步验证了完全优化的测定法。总之,本研究中开发的基于复制子细胞的 HTS 测定法将有助于发现针对寨卡病毒的抗病毒化合物。

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