变构调节
蛋白质酪氨酸磷酸酶
磷酸酶
活动站点
化学
生物化学
药物发现
结合位点
酪氨酸
变构酶
生物
酶
作者
Christian Wiesmann,Kenneth J. Barr,Jenny Kung,Jiang Zhu,Daniel A. Erlanson,Shen Wang,Bruce J Fahr,Min Zhong,Lisa J. Taylor,Mike Randal,Robert S. McDowell,Steven G. Hansen
摘要
Obesity and type II diabetes are closely linked metabolic syndromes that afflict >100 million people worldwide. Although protein tyrosine phosphatase 1B (PTP1B) has emerged as a promising target for the treatment of both syndromes, the discovery of pharmaceutically acceptable inhibitors that bind at the active site remains a substantial challenge. Here we describe the discovery of an allosteric site in PTP1B. Crystal structures of PTP1B in complex with allosteric inhibitors reveal a novel site located approximately 20 A from the catalytic site. We show that allosteric inhibitors prevent formation of the active form of the enzyme by blocking mobility of the catalytic loop, thereby exploiting a general mechanism used by tyrosine phosphatases. Notably, these inhibitors exhibit selectivity for PTP1B and enhance insulin signaling in cells. Allosteric inhibition is a promising strategy for targeting PTP1B and constitutes a mechanism that may be applicable to other tyrosine phosphatases.
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