Käck H, Sjögren T
Protein Sciences, Structure and Biophysics, Discovery Sciences, BioPharmaceuticals R&D, AstraZeneca, Pepparedsleden 1, SE-431 50 Gothenburg, Sweden.
J Synchrotron Radiat. 2025 Mar 1;32(Pt 2):294-303. doi: 10.1107/S1600577524012281. Epub 2025 Feb 6.
Structure-based drug design has been an integral part of drug discovery for over three decades, contributing to the development of numerous approved drugs. Here we discuss the evolution, as well as the current state, of structure-based drug design within the pharmaceutical industry, using data from AstraZeneca's internal repository for crystal structures to provide additional context. Over the past 20 years, the company has transitioned from a mixed in-house and synchrotron data collection model to a `synchrotron-only' approach, enabled by technological advancements at synchrotron facilities. We provide real-world examples of structure delivery to projects, including a high-throughput project and a case where a single structure was pivotal for discovering a candidate drug. We conclude that, despite recent developments in single-particle cryo-EM and deep-learning structure prediction methods, macromolecular crystallography remains a critical tool for drug discovery.
基于结构的药物设计在过去三十多年里一直是药物研发不可或缺的一部分,推动了众多获批药物的开发。在此,我们利用阿斯利康内部晶体结构数据库的数据,探讨制药行业中基于结构的药物设计的发展历程以及现状,以提供更多背景信息。在过去20年里,由于同步辐射设施的技术进步,该公司已从内部和同步辐射混合数据收集模式转变为“仅使用同步辐射”的方法。我们提供了向项目交付结构的实际案例,包括一个高通量项目以及一个单一结构对发现候选药物起关键作用的案例。我们得出结论,尽管单颗粒冷冻电镜和深度学习结构预测方法最近有所发展,但大分子晶体学仍然是药物研发的关键工具。