Weirath Nicholas A, Haskell-Luevano Carrie
Department of Medicinal Chemistry & Institute for Translational Neuroscience, University of Minnesota, Minneapolis, Minnesota 55455, United States.
ACS Pharmacol Transl Sci. 2024 Aug 26;7(9):2706-2724. doi: 10.1021/acsptsci.4c00129. eCollection 2024 Sep 13.
The melanocortin receptors are a centrally and peripherally expressed family of Class A GPCRs with physiological roles, including pigmentation, steroidogenesis, energy homeostasis, and others yet to be fully characterized. There are five melanocortin receptor subtypes that, apart from the melanocortin-2 receptor (MC2R), are stimulated by a shared set of endogenous agonists. Until 2020, X-ray crystallographic and cryo-electron microscopic (cryo-EM) structures of these receptors were unavailable, and the investigation of their mechanisms of action and putative ligand-receptor interactions was driven by site-directed mutagenesis studies of the receptors and targeted structure-activity relationship (SAR) studies of the endogenous and derivative synthetic ligands. Synthetic derivatives of the endogenous agonist ligand α-MSH have evolved into a suite of powerful ligands such as NDP-MSH (melanotan I), melanotan II (MTII), and SHU9119. This suite of tool compounds now enables the study of the melanocortin receptors and serves as scaffolds for FDA-approved drugs, means of validating stably expressing melanocortin receptor cell lines, core ligands in assessing cryo-EM structures of active and inactive receptor complexes, and essential references for high-throughput discovery and mechanism of action studies. Herein, we review the history and significance of a finite set of these essential tool compounds and discuss how they are being utilized to further the field's understanding of melanocortin receptor physiology and greater druggability.
黑皮质素受体是一类在中枢和外周表达的A类G蛋白偶联受体家族,具有多种生理作用,包括色素沉着、类固醇生成、能量稳态等,还有一些作用尚未完全明确。黑皮质素受体有五种亚型,除黑皮质素-2受体(MC2R)外,其余亚型均由一组共同的内源性激动剂激活。直到2020年,这些受体的X射线晶体学和冷冻电子显微镜(cryo-EM)结构仍未获得,对其作用机制和假定的配体-受体相互作用的研究主要基于受体的定点诱变研究以及内源性和衍生合成配体的靶向构效关系(SAR)研究。内源性激动剂配体α-MSH的合成衍生物已发展成为一系列强大的配体,如NDP-MSH(黑素皮质素I)、黑素皮质素II(MTII)和SHU9119。这一系列工具化合物现在可用于研究黑皮质素受体,并作为FDA批准药物的支架,用于验证稳定表达黑皮质素受体的细胞系,评估活性和非活性受体复合物冷冻电镜结构的核心配体,以及高通量发现和作用机制研究的重要参考。在此,我们回顾了这些重要工具化合物中的一组的历史和意义,并讨论了它们如何被用于加深该领域对黑皮质素受体生理学的理解以及提高药物可及性。