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A novel cell-based 384-well, label-free assay for discovery of inhibitors of influenza A virus

机译:一种新型的基于细胞的384孔无标记测定法,用于发现甲型流感病毒的抑制剂

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Abstract: Resonance wave-guide (RWG) biosensor technology allows label-free measurements of global cellular responses of the dynamic mass redistribution (DMR). We hypothesized that the DMR signals to extracellular stimulations occurring upon entry of a virus, could provide a new approach for the development of physiologically relevant cell-based assays for screening of small molecules. We explored this technology with influenza virus (A/Udorn/72, H3N2) using MDCK and Vero E6 cell lines in a 384-well format. The MDCK cell line assay was optimized with a fibronectin-coated surface microplate with 6000 cells per well that were infected at a multiplicity of infection (MOI) of 1. Under this set of optimized conditions, for the vero E6 cells, an assay window of 1130 pm shift were obtained at 24 hours. The Vero E6 cell line assay was optimized using a poly-D-lysine-coated surface with seeding density of 6000 cells per well that were infected at a MOI of 5. Under this set of optimized conditions for the MDCK cells, an assay window of >600 units and Z values of 0.6–0.7 were obtained at 24 h. A small library of 1120 compounds was screened using the MDCK, which demonstrates the feasibility of the approach for high-throughput screening.
机译:摘要:共振波导(RWG)生物传感器技术可对动态质量重新分布(DMR)的整体细胞反应进行无标签测量。我们假设DMR信号进入病毒后会发生细胞外刺激,可以为筛选小分子的生理相关的基于细胞的测定方法的开发提供新的方法。我们使用384孔格式的MDCK和Vero E6细胞系探索了这种技术与流感病毒(A / Udorn / 72,H3N2)。 MDCK细胞系分析用纤连蛋白包被的表面微孔板优化,每孔6000个细胞,感染复数(MOI)为1。在这组优化条件下,对于vero E6细胞,其检测窗口为在24小时获得了1130 pm的班次。使用聚-D-赖氨酸包被的表面优化了Vero E6细胞系的测定,接种密度为每孔6000个细胞,以MOI为5感染。在MDCK细胞的这组优化条件下,测定窗口为在24小时内获得了> 600个单位,Z值为0.6-0.7。使用MDCK筛选了1120个化合物的小型文库,这证明了该方法用于高通量筛选的可行性。

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