Model-Based Discovery of Synthetic Agonists for the Zn-Sensing G-Protein-Coupled Receptor 39 (GPR39) Reveals Novel Biological Functions.

The G-protein-coupled receptor 39 (GPR39) is a G-protein-coupled receptor activated by Zn. We used a homology model-based approach to identify small-molecule pharmacological tool compounds for the receptor. The method focused on a putative binding site in GPR39 for synthetic ligands and knowledge of ligand binding to other receptors with similar binding pockets to select iterative series of minilibraries. These libraries were cherry-picked from all commercially available synthetic compounds. A total of only 520 compounds were tested in vitro, making this method broadly applicable for tool compound development. The compounds of the initial library were inactive when tested alone, but lead compounds were identified using Zn as an allosteric enhancer. Highly selective, highly potent Zn-independent GPR39 agonists were found in subsequent minilibraries. These agonists identified GPR39 as a novel regulator of gastric somatostatin secretion.