Ahn Kay, Boehm Markus, Brown Matthew F, Calloway Jessica, Che Ye, Chen Jinshan, Fennell Kimberly F, Geoghegan Kieran F, Gilbert Adam M, Gutierrez Jemy A, Kalgutkar Amit S, Lanba Adhiraj, Limberakis Chris, Magee Thomas V, O'Doherty Inish, Oliver Robert, Pabst Brandon, Pandit Jayvardhan, Parris Kevin, Pfefferkorn Jeffrey A, Rolph Timothy P, Patel Rushi, Schuff Brandon, Shanmugasundaram Veerabahu, Starr Jeremy T, Varghese Alison H, Vera Nicholas B, Vernochet Cecile, Yan Jiangli
Cardiovascular, Metabolic, and Endocrine Diseases (CVMED) Research Unit, Pfizer Inc. , 610 Main Street, Cambridge, Massachusetts 02139, United States.
Worldwide Medicinal Chemistry and §Pharmacokinetics, Dynamics, & Metabolism, Pfizer Inc. , Eastern Point Road, Groton, Connecticut 06340, United States.
ACS Chem Biol. 2016 Sep 16;11(9):2529-40. doi: 10.1021/acschembio.6b00266. Epub 2016 Jul 19.
Lysophospholipase-like 1 (LYPLAL1) is an uncharacterized metabolic serine hydrolase. Human genome-wide association studies link variants of the gene encoding this enzyme to fat distribution, waist-to-hip ratio, and nonalcoholic fatty liver disease. We describe the discovery of potent and selective covalent small-molecule inhibitors of LYPLAL1 and their use to investigate its role in hepatic metabolism. In hepatocytes, selective inhibition of LYPLAL1 increased glucose production supporting the inference that LYPLAL1 is a significant actor in hepatic metabolism. The results provide an example of how a selective chemical tool can contribute to evaluating a hypothetical target for therapeutic intervention, even in the absence of complete biochemical characterization.
溶血磷脂酶样1(LYPLAL1)是一种尚未明确其功能的代谢性丝氨酸水解酶。全基因组关联研究表明,编码该酶的基因变体与脂肪分布、腰臀比及非酒精性脂肪性肝病相关。我们描述了LYPLAL1强效且选择性共价小分子抑制剂的发现及其在研究该酶在肝脏代谢中作用的应用。在肝细胞中,对LYPLAL1的选择性抑制增加了葡萄糖生成,支持了LYPLAL1是肝脏代谢中重要参与者的推断。这些结果提供了一个示例,说明即使在缺乏完整生化特征的情况下,一种选择性化学工具如何有助于评估作为治疗干预的假定靶点。