Arimont Marta, Sun Shan-Liang, Leurs Rob, Smit Martine, de Esch Iwan J P, de Graaf Chris
Division of Medicinal Chemistry, Faculty of Sciences, Amsterdam Institute of Molecules, Medicines and Systems (AIMMS), Vrije Universiteit Amsterdam , De Boelelaan 1108, 1081 HZ Amsterdam, The Netherlands.
J Med Chem. 2017 Jun 22;60(12):4735-4779. doi: 10.1021/acs.jmedchem.6b01309. Epub 2017 Mar 10.
This review focuses on the construction and application of structural chemokine receptor models for the elucidation of molecular determinants of chemokine receptor modulation and the structure-based discovery and design of chemokine receptor ligands. A comparative analysis of ligand binding pockets in chemokine receptors is presented, including a detailed description of the CXCR4, CCR2, CCR5, CCR9, and US28 X-ray structures, and their implication for modeling molecular interactions of chemokine receptors with small-molecule ligands, peptide ligands, and large antibodies and chemokines. These studies demonstrate how the integration of new structural information on chemokine receptors with extensive structure-activity relationship and site-directed mutagenesis data facilitates the prediction of the structure of chemokine receptor-ligand complexes that have not been crystallized. Finally, a review of structure-based ligand discovery and design studies based on chemokine receptor crystal structures and homology models illustrates the possibilities and challenges to find novel ligands for chemokine receptors.
本综述聚焦于构建和应用结构趋化因子受体模型,以阐明趋化因子受体调控的分子决定因素,以及基于结构发现和设计趋化因子受体配体。文中对趋化因子受体中配体结合口袋进行了比较分析,包括对CXCR4、CCR2、CCR5、CCR9和US28的X射线结构的详细描述,及其对模拟趋化因子受体与小分子配体、肽配体、大型抗体和趋化因子分子相互作用的意义。这些研究表明,将趋化因子受体新的结构信息与广泛的构效关系和定点诱变数据相结合,如何有助于预测尚未结晶的趋化因子受体-配体复合物的结构。最后,对基于趋化因子受体晶体结构和同源模型的基于结构的配体发现和设计研究的综述,阐明了寻找趋化因子受体新配体的可能性和挑战。