Recent progress in fragment-based drug discovery facilitated by NMR spectroscopy

Lei Wang , Jia Gao , Rongsheng Ma , Yaqian Liu , Mingqing Liu , Fumei Zhong , Jie Hu , Shuju Li , Jihui Wu , Hualiang Jiang , Jiahai Zhang , Ke Ruan
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引用次数: 3

Abstract

Considerable developments have been observed in fragment-based lead/drug discovery (FBLD/FBDD) recently, with four drugs approved and many others under investigation. Nuclear magnetic resonance (NMR) has gained increasing popularity in FBLD due to its intrinsic capability in characterizing protein-ligand interactions in a large dynamic range of affinity, from weak hits to highly potent drugs. Here, we summarize NMR applications in fragment-based hit-to-lead evolution, including the construction of a fragment library, screening methods, spectra processing, and the delineation of the protein-ligand binding modes. These state-of-the-art NMR techniques have been exemplified in the discovery of inhibitors against multiple targets over the past five years, and they are expected to continue to provide new insights in the future.

Abstract Image

核磁共振波谱促进基于片段的药物发现的最新进展
最近,在基于片段的先导物/药物发现(FBLD/FBDD)方面取得了相当大的进展,有四种药物获得批准,其他许多药物正在研究中。核磁共振(NMR)在FBLD中越来越受欢迎,因为它具有在大动态亲和力范围内表征蛋白质-配体相互作用的内在能力,从弱撞击到强效药物。在这里,我们总结了核磁共振在基于片段的hit-to-lead进化中的应用,包括片段库的构建、筛选方法、光谱处理以及蛋白质-配体结合模式的描述。在过去的五年中,这些最先进的核磁共振技术已经在发现针对多个目标的抑制剂中得到了证明,并且预计它们将在未来继续提供新的见解。
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来源期刊
Magnetic Resonance Letters
Magnetic Resonance Letters Analytical Chemistry, Spectroscopy, Radiology and Imaging, Biochemistry, Genetics and Molecular Biology (General)
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