Competitive Activity-Based Protein Profiling Identifies Aza-尾-Lactams as a Versatile Chemotype for Serine Hydrolase Inhibition

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• 作者：Andrea M. Zuhl ; Justin T. Mohr ; Daniel A. Bachovchin ; Sherry Niessen ; Ku-Lung Hsu ; Jacob M. Berlin ; Maximilian Dochnahl ; Mar铆a P. L贸pez-Alberca ; Gregory C. Fu ; Benjamin F. Cravatt
• 刊名：The Journal of the American Chemical Society
• 出版年：2012
• 出版时间：March 21, 2012
• 年：2012
• 卷：134
• 期：11
• 页码：5068-5071
• 全文大小：282K
• 年卷期：v.134,no.11(March 21, 2012)
• ISSN：1520-5126

文摘

Serine hydrolases are one of the largest and most diverse enzyme classes in Nature. Most serine hydrolases lack selective inhibitors, which are valuable probes for assigning functions to these enzymes. We recently discovered a set of aza-尾-lactams (ABLs) that act as potent and selective inhibitors of the mammalian serine hydrolase protein-phosphatase methylesterase-1 (PME-1). The ABLs inactivate PME-1 by covalent acylation of the enzyme鈥檚 serine nucleophile, suggesting that they could offer a general scaffold for serine hydrolase inhibitor discovery. Here, we have tested this hypothesis by screening ABLs more broadly against cell and tissue proteomes by competitive activity-based protein profiling (ABPP), leading to the discovery of lead inhibitors for several serine hydrolases, including the uncharacterized enzyme 伪,尾-hydrolase domain-containing 10 (ABHD10). ABPP-guided medicinal chemistry yielded a compound ABL303 that potently (IC₅₀ 鈮?30 nM) and selectively inactivated ABHD10 in vitro and in living cells. A comparison of optimized inhibitors for PME-1 and ABHD10 indicates that modest structural changes that alter steric bulk can tailor the ABL to selectively react with distinct, distantly related serine hydrolases. Our findings, taken together, designate the ABL as a versatile reactive group for creating first-in-class serine hydrolase inhibitors.