| Literature DB >> 23863939 |
Kaspar Hollenstein1, James Kean, Andrea Bortolato, Robert K Y Cheng, Andrew S Doré, Ali Jazayeri, Robert M Cooke, Malcolm Weir, Fiona H Marshall.
Abstract
Structural analysis of class B G-protein-coupled receptors (GPCRs), cell-surface proteins that respond to peptide hormones, has been restricted to the amino-terminal extracellular domain, thus providing little understanding of the membrane-spanning signal transduction domain. The corticotropin-releasing factor receptor type 1 is a class B receptor which mediates the response to stress and has been considered a drug target for depression and anxiety. Here we report the crystal structure of the transmembrane domain of the human corticotropin-releasing factor receptor type 1 in complex with the small-molecule antagonist CP-376395. The structure provides detailed insight into the architecture of class B receptors. Atomic details of the interactions of the receptor with the non-peptide ligand that binds deep within the receptor are described. This structure provides a model for all class B GPCRs and may aid in the design of new small-molecule drugs for diseases of brain and metabolism.Entities:
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Year: 2013 PMID: 23863939 DOI: 10.1038/nature12357
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 49.962