Josiah Serene
Cambridge, MA, USA.
Methods Mol Biol. 2009;486:177-92. doi: 10.1007/978-1-60327-545-3_13.
High-throughput screening (HTS) covers a range of measurements, from primary screens of either large libraries (>250 K) or small, focused collections (100-1,000 s) of test compounds, to secondary screens used to characterize the mechanism of action of a relatively small number of compounds. Data analysis of assay results from HTS relies upon assay performance and the control wells used to define the assay system. This chapter discusses parameters that must be considered when defining controls and plate maps for primary and secondary assays in HTS. Control wells and plate maps are suggested, which can gene-rally be applied toward a variety of biochemical and cellular assays. The controls and plate-map options can be matched to the scale of the screening campaign; examples are primary screens with % inhibition or % activation as endpoints or secondary screens with IC(50) or EC(50) values as endpoints.
高通量筛选(HTS)涵盖一系列测量方法,从对大型文库(>250,000)或小型、针对性强的测试化合物集合(100 - 1,000种)进行的初筛,到用于表征相对少量化合物作用机制的复筛。高通量筛选分析结果的数据分析依赖于分析性能以及用于定义分析系统的对照孔。本章讨论在为高通量筛选中的初筛和复筛定义对照和板图时必须考虑的参数。文中给出了对照孔和板图建议,这些建议通常可应用于各种生化和细胞分析。对照和板图选项可与筛选活动的规模相匹配;例如,以抑制率或激活率为终点的初筛,或以IC(50)或EC(50)值为终点的复筛。