Journal
BIOORGANIC & MEDICINAL CHEMISTRY
Volume 40, Issue -, Pages -Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bmc.2021.116179
Keywords
Glycogen synthase kinase 3; Cell signaling; Alzheimer's disease; Sepsis; Serine/threonine protein kinase; Enzyme inhibitor; Tideglusib
Funding
- National Institutes of Health [R15GM110602]
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COB-187 inhibits GSK3 beta via a specific, reversible, time and Cys-199-dependent mechanism, demonstrating high selectivity and potent activity against the target enzyme.
Glycogen synthase kinase-3 (GSK-3) has been implicated in numerous pathologies making GSK-3 an attractive therapeutic target. Our group has identified a compound termed COB-187 that is a potent and selective inhibitor of GSK-3. In this study, we probed the mechanism by which COB-187 inhibits GSK-3 beta. Progress curves, generated via real-time monitoring of kinase activity, indicated that COB-187 inhibition of GSK-3 beta is time-dependent and subsequent jump dilution assays revealed that COB-187 binding to GSK-3 beta is reversible. Further, a plot of the kinetic constant (kobs) versus COB-187 concentration suggested that, within the range of concentrations studied, COB-187 binds to GSK-3 beta via an induced-fit mechanism. There is a critical cysteine residue at the entry to the active site of GSK-3 beta (Cys-199). We generated a mutant version of GSK-3 beta wherein Cys-199 was substituted with an alanine. This mutation caused a dramatic decrease in the activity of COB-187; specifically, an IC50 in the nM range for wild type versus >100 mu M for the mutant. A screen of COB-187 against 34 kinases that contain a conserved cysteine in their active site revealed that COB-187 is highly selective for GSK-3 indicating that COB187's inhibition of GSK-3 beta via Cys-199 is specific. Combined, these findings suggest that COB-187 inhibits GSK3 beta via a specific, reversible, time and Cys-199-dependent mechanism.
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