a Department of Biosciences and Centre for Global Infectious Disease , Durham University , Durham , UK.
Expert Opin Drug Discov. 2018 Dec;13(12):1153-1160. doi: 10.1080/17460441.2018.1534826. Epub 2018 Oct 16.
: Both biochemical and phenotypic assay platforms have clear limitations in high throughput screening (HTS) for drug discovery. The use of genetically tractable model yeast as a vehicle for target-based HTS overcomes many of these by allowing the identification of on-target compounds that function within a eukaryotic cellular context. : In this special report, the use of yeast-based assays in HTS is discussed with reference to the various platforms that have been utilized over the past 20 years. The specific issues considered are the necessity to employ counter and secondary screening approaches to ensure the on-target activity of hits, and the recent developments in detection systems that have facilitated miniaturization and ultra-HTS. : It is difficult at present to predict the future. That being said, the demonstrable possibilities of optimizing yeast-based HTS, coupled with the demonstration of utility in an industrial setting, shows that these platforms have the potential to bridge the gap between phenotypic and biochemical assays for HTS.
: 在药物发现的高通量筛选(HTS)中,生化和表型测定平台都有明显的局限性。利用遗传上可操作的模式酵母作为基于靶标的 HTS 的载体,可以克服许多这些局限性,从而可以识别在真核细胞环境中起作用的靶标化合物。在本专题报告中,将讨论在 HTS 中使用酵母测定法,并参考过去 20 年来使用的各种平台。考虑的具体问题是有必要采用对照和辅助筛选方法来确保命中的靶标活性,以及最近在检测系统方面的发展,这些发展促进了微型化和超 HTS。目前很难预测未来。话虽如此,酵母基 HTS 的优化的可能性已经得到了证明,并且在工业环境中的实用性也得到了证明,这表明这些平台有可能弥合 HTS 中表型和生化测定之间的差距。