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Simple Absorbance-Based Assays for Ultra-High Throughput Screening

机译:基于吸光度的简单分析方法,用于超高通量筛选

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In order to accommodate the predicted increase in screening required of successful pharmaceutical companies, miniaturized, high-speed HTS formats are necessary. Much emphasis has been placed on sensitive fluorescence techniques, but some systems, particularly enzymes interconverting small substrates, are likely to be refractory to such approaches. We show here that simple absorbance-based assays can be miniaturized to 10-μl volumes in 1536-well microplates compatible with the requirements for ultra-high throughput screening. We demonstrate that, with low-cost hardware, assay performance is wholly predictable from the 2-fold decrease in pathlength for fully filled 1536-well plates compared to 96- and 384-well microplates. A number of enzyme systems are shown to work in this high-density format, and the inhibition parameters determined are comparable with those in standard assay formats. We also demonstrate the utility of kinetics measurements in miniaturized format with improvements in assay quality and the ability to extract detailed mechanistic information about inhibitors.
机译:为了适应成功制药公司对筛查的预期增加,小型化,高速HTS格式是必要的。人们已经将许多重点放在灵敏的荧光技术上,但是某些系统,特别是将小底物相互转化的酶,可能对这种方法不具吸引力。我们在这里表明,可以在1536孔微孔板中将基于吸光度的简单测定法小型化至10 µl体积,以满足超高通量筛选的要求。我们证明,与96和384孔微孔板相比,完全填充的1536孔板的光程长度降低2倍,使用低成本硬件可以完全预测分析性能。已显示许多酶系统以这种高密度形式工作,并且所确定的抑制参数与标准测定形式中的那些相当。我们还展示了以小型化形式进行动力学测量的实用性,并提高了测定质量,并能够提取有关抑制剂的详细机械信息。

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