吞吐量
计算机科学
高通量筛选
可靠性(半导体)
生物信息学
生物
物理
操作系统
量子力学
功率(物理)
无线
作者
Hannah Rowlands,Kirsten Tschapalda,Carolyn Blackett,Delyan P. Ivanov,Darren Plant,Joseph Shaw,Andrew P. Thomas,Martin J. Packer,Laurence Arnold,Geoffrey A. Holdgate
标识
DOI:10.1016/j.slasd.2023.01.006
摘要
The cellular thermal shift assay (CETSA®) has increasingly been used in early drug discovery to provide a measure of cellular target engagement. Traditionally, CETSA has been employed for bespoke questions with small to medium throughput and has predominantly been applied during hit validation rather than in hit identification. Using a CETSA screen versus the kinase CRAF, we assessed 3 key questions: (1) technical feasibility - could the CETSA methodology technically be applied at truly high throughput scale? (2) relevance - could hits suitable for further optimisation be identified? (3) reliability - would the approach identify known chemical equity. Here, we describe the first large scale AlphaLISA SureFire based CETSA (Alpha CETSA) approach allowing us to screen a large library of almost 0.5 million compounds. We discuss the issues overcome in automating and executing the screen and describe the resulting screen output.
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