Lavis, Trento, Italy.
Bio Structure and Biophysics, Integrated Drug Discovery, Sanofi R&D, 13, Quai Jules Guesde-BP 14, 94403, Vitry sur Seine Cedex, France.
ChemMedChem. 2019 Jun 5;14(11):1115-1127. doi: 10.1002/cmdc.201900152. Epub 2019 May 14.
Ligand-based NMR screening represents a powerful method in fragment-based drug discovery for the identification of chemical matter interacting with the receptor of interest. The large dynamic range of these methods allows the detection of weakly binding ligands. However, the methodology has not been extensively used for quantifying the strength of these interactions. This knowledge is important for ranking fragments according to their binding strength and for prioritizing structure-based and medicinal chemistry activities. Rapid NMR methods for measuring the dissociation constant in direct and competition modes are presented here. The theory underpinning these methods are presented, along with their application to the measurement of the binding affinities of several ligands of the heat shock protein 90.
基于配体的 NMR 筛选代表了一种在基于片段的药物发现中用于鉴定与靶受体相互作用的化学物质的强大方法。这些方法的动态范围很大,可以检测到弱结合的配体。然而,该方法尚未广泛用于定量这些相互作用的强度。这种知识对于根据结合强度对片段进行排序以及对基于结构和药物化学的活性进行优先级排序非常重要。本文介绍了用于直接和竞争模式测量离解常数的快速 NMR 方法。本文介绍了这些方法的理论基础及其在测量热休克蛋白 90 的几种配体的结合亲和力中的应用。