糖皮质激素受体
计算生物学
药物发现
糖皮质激素
蛋白质-蛋白质相互作用
受体
化学
计算机科学
生物
生物化学
内分泌学
作者
Matthew W. D. Perry,Claire C. Munier,João Augusto de Castro Neves,Anders Gunnarsson,Fredrik Edfeldt,Isabelle Landrieu,Christian Ottmann
标识
DOI:10.26434/chemrxiv-2024-g85dm
摘要
Given the importance of glucocorticoid receptor (GR) agonists in medicine, despite their numerous adverse side effects, it is of great interest to fully delineate the regulatory network of GR. Post-translational modifications form part of this regulatory network including phosphorylation. After phosphorylation GR interacts with 14-3-3, adding another layer of regulation beyond the ligand-driven activation. Here, we use a screening strategy inspired from traditional hit-finding methods for prospective identification of the first de novo molecular glues of the GR–14-3-3 protein-protein interactions (PPI). Screening 8,000 compounds led to the discovery of one hit. To foster confidence in its stabilisation activity, this hit was further investigated in an array of experiments using biophysical assays, 1D and 2D NMR spectroscopy, and analysis of near neighbours outlined initial structure activity relationships. In addition, those early chemical probes provide starting points for future development into potent tool compounds which could contribute to answer the long-standing question of the physiological role of the GR–14-3-3 PPI.
科研通智能强力驱动
Strongly Powered by AbleSci AI