Hevener Kirk E, Pesavento Russell, Ren JinHong, Lee Hyun, Ratia Kiira, Johnson Michael E
Department of Pharmaceutical Sciences, University of Tennessee Health Science Center, Memphis, TN, United States.
Center for Biomolecular Sciences, University of Illinois at Chicago, Chicago, IL, United States; College of Dentistry, University of Illinois at Chicago, Chicago, IL, United States.
Methods Enzymol. 2018;610:265-309. doi: 10.1016/bs.mie.2018.09.022. Epub 2018 Oct 25.
High-throughput screening assays have become nearly ubiquitous in the search for small compounds or peptides that can modulate biological processes for therapeutic purposes. While many assays have become quite robust, with well-established protocols, the subsequent steps of validating the hits and choosing the best ones to take forward into leads for further chemical development are less established. In this chapter, we describe a variety of approaches, including chemical assessment, the use of various computational approaches, a variety of counter-screens, and "orthogonal" biophysical assays using nuclear magnetic resonance, surface plasmon resonance, isothermal titration calorimetry or thermal shift assays as methods for validating and assessing the quality of hits.
高通量筛选分析在寻找可调节生物过程以用于治疗目的的小分子化合物或肽的过程中几乎无处不在。虽然许多分析已经相当成熟,有完善的方案,但后续验证筛选出的活性物质并选择最佳的物质以推进到先导物进行进一步化学开发的步骤却不太成熟。在本章中,我们描述了多种方法,包括化学评估、使用各种计算方法、各种反筛选,以及使用核磁共振、表面等离子体共振、等温滴定量热法或热位移分析等“正交”生物物理分析作为验证和评估筛选出的活性物质质量的方法。