化学
酶
DNA
生物化学
血清素
DNA修复
立体化学
受体
作者
Marek Varga,Florian Ortis,Alicia del Prado,Alice Eddershaw,Emma Rose Scaletti,Emily C. Hank,Kaixin Zhou,Natálie Rudolfová,Alessia Dodaro,Elisée Wiita,Ingrid Almlöf,Stella Karsten,Kirill Mamonov,Sabbir Ahmed,Kirsty Bentley,Olov Wallner,Evert Homan,Martin Scobie,Thomas Helleday,Mario Prejanò
标识
DOI:10.1021/acs.jmedchem.5c01454
摘要
The base excision repair enzyme 8-oxoguanine DNA glycosylase 1 (OGG1) plays a central role in maintaining genome integrity and mediating cellular responses to oxidative stress. As such, it represents an attractive target for pharmaceutical modulation. Small-molecule organocatalytic switches (ORCAs) greatly enhance the rate of OGG1-catalyzed cleavage of DNA abasic sites, thereby accelerating DNA repair. Here, we present the discovery and hit-to-lead optimization of a novel class of highly potent serotonin-derived ORCAs with greatly improved pharmacokinetic properties. Biochemical assays, X-ray crystallography, and molecular dynamics simulations point toward a water-mediated mechanism of activation, distinct from previously proposed Brønsted base-assisted models. These findings establish serotonin-based ORCAs as promising chemical probes and potential leads for therapeutic modulation of OGG1 in oxidative stress-driven diseases.
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