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Automated cell-based luminescence assay for profiling antiviral compound activity against enteroviruses

机译:基于细胞的自动发光测定法可分析抗肠道病毒的抗病毒化合物活性

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We describe the development, optimisation, and validation of an automated, cell-based and high-throughput screening assay using existing luminescence-based ATPlite reagents for identifying antiviral compounds that inhibit enterovirus replication. Antiviral efficacy was determined by measuring the ATP levels in cells that were protected from the viral cytopathic effect (CPE) by the antiviral compounds pleconaril and rupintrivir. CPE-based assay conditions were optimised at a cell density of 5000 cells/well and a viral infection dose of 100 CCIDsub50/sub in 384-well plates. The assay exhibited excellent robustness, with Z'-factor values between 0.75 and 0.82, coefficients of variation between 0.33% and 1.45%, and signal-to-background ratios ranging from 6.92 to 22.6 when testing three enterovirus A71 isolates circulating in China. The assay was also suitable for screening other picornaviruses, such as poliovirus, coxsackievirus, echovirus, and parechovirus.
机译:我们描述了使用现有的基于发光的ATPlite试剂来鉴定抑制肠病毒复制的抗病毒化合物的自动化,基于细胞和高通量筛选测定的开发,优化和验证。通过测量被抗病毒化合物pleconaril和rupintrivir保护免受病毒细胞病作用(CPE)的细胞中的ATP水平,确定抗病毒效力。在384孔板中以5000个细胞/孔的细胞密度和100 CCID 50 的病毒感染剂量优化了基于CPE的测定条件。该测定法显示出出色的鲁棒性,当测试在中国流通的三种肠病毒A71分离株时,Z'因子值在0.75至0.82之间,变异系数在0.33%至1.45%之间,信噪比在6.92至22.6之间。该测定法还适用于筛选其他小核糖核酸病毒,例如脊髓灰质炎病毒,柯萨奇病毒,回声病毒和副猪病毒。

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