bioRxiv · 10.1101/2022.01.05.474995
Cryo-EM structure of human somatostatin receptor 2 complex with its agonist somatostatin delineates the ligand binding specificity
Abstract
Somatostatin is a peptide hormone regulating endocrine systems through binding to G-protein-coupled somatostatin receptors. somatostatin receptor 2 (SSTR2) is one of the human somatostatin receptors and highly implicated in cancers and neurological disorders. Here, we report the high resolution cryo-EM structure of full-length human SSTR2 bound to the agonist somatostatin (SST-14) complex with inhibitory G (Gi) proteins. Our structure shows that seven transmembrane helices form a deep pocket for ligand binding and that the highly conserved Trp-Lys motif of SST-14 positions at the bottom of the pocket. Furthermore, our sequence analysis combined with AlphaFold modeled structures of other SSTR isoforms provide how SSTR family proteins specifically interact with their cognate ligands. This work provides the first glimpse into the molecular recognition of somatostatin receptor and crucial resource to develop therapeutics targeting somatostatin receptors.
Source connections
Explore related subjects
Keep this discovery
Explore connections, maps & timelines
Heo, Y., Yoon, E., Jeon, Y.-E., Yun, J.-H., Ishimoto, N., Woo, H., Park, S.-Y., Song, J.-J., Lee, W.. 2022-01-05. Cryo-EM structure of human somatostatin receptor 2 complex with its agonist somatostatin delineates the ligand binding specificity. https://doi.org/10.1101/2022.01.05.474995
Cite the original work for its findings. Save a collection to share your selection of sources.