Genick Christine C, Wright S Kirk
a Novartis Pharma AG, Novartis Institutes for BioMedical Research, Chemical Biology and Therapeutics , Protein Sciences , Basel , Switzerland.
b Protein Sciences, Research Parkway Meriden , Cambridge , MA , USA.
Expert Opin Drug Discov. 2017 Sep;12(9):897-907. doi: 10.1080/17460441.2017.1349096. Epub 2017 Jul 6.
There are many challenges to the drug discovery process, including the complexity of the target, its interactions, and how these factors play a role in causing the disease. Traditionally, biophysics has been used for hit validation and chemical lead optimization. With its increased throughput and sensitivity, biophysics is now being applied earlier in this process to empower target characterization and hit finding. Areas covered: In this article, the authors provide an overview of how biophysics can be utilized to assess the quality of the reagents used in screening assays, to validate potential tool compounds, to test the integrity of screening assays, and to create follow-up strategies for compound characterization. They also briefly discuss the utilization of different biophysical methods in hit validation to help avoid the resource consuming pitfalls caused by the lack of hit overlap between biophysical methods. Expert opinion: The use of biophysics early on in the drug discovery process has proven crucial to identifying and characterizing targets of complex nature. It also has enabled the identification and classification of small molecules which interact in an allosteric or covalent manner with the target. By applying biophysics in this manner and at the early stages of this process, the chances of finding chemical leads with novel mechanisms of action are increased. In the future, focused screens with biophysics as a primary readout will become increasingly common.
药物研发过程面临诸多挑战,包括靶点的复杂性、其相互作用以及这些因素在致病过程中如何发挥作用。传统上,生物物理学一直用于活性筛选验证和化学先导物优化。随着其通量和灵敏度的提高,生物物理学现在在此过程中更早地得到应用,以助力靶点表征和活性筛选。涵盖领域:在本文中,作者概述了生物物理学如何用于评估筛选试验中所用试剂的质量、验证潜在的工具化合物、测试筛选试验的完整性以及制定化合物表征的后续策略。他们还简要讨论了不同生物物理方法在活性筛选验证中的应用,以帮助避免因生物物理方法之间缺乏活性重叠而导致的资源消耗陷阱。专家观点:在药物研发过程早期使用生物物理学已被证明对于识别和表征复杂性质的靶点至关重要。它还能够识别和分类以变构或共价方式与靶点相互作用的小分子。通过以这种方式并在此过程的早期阶段应用生物物理学,发现具有新作用机制的化学先导物的机会增加。未来,以生物物理学作为主要读数的聚焦筛选将变得越来越普遍。