Application of an Integrated GPCR SAR-Modeling Platform To Explain the Activation Selectivity of Human 5‑HT2C over 5‑HT2B

• Published in: ACS chemical biology Vol. 11; no. 5; pp. 1372 - 1382
• Main Authors: Heifetz, Alexander, Storer, R. Ian, McMurray, Gordon, James, Tim, Morao, Inaki, Aldeghi, Matteo, Bodkin, Mike J, Biggin, Philip C
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 20.05.2016
• Subjects: Amino Acid Sequence; Azepines - chemistry; Azepines - pharmacology; Crystallography, X-Ray; Drug Design; Humans; Protein Conformation; Receptor, Serotonin, 5-HT2B - chemistry; Receptor, Serotonin, 5-HT2B - metabolism; Receptor, Serotonin, 5-HT2C - chemistry; Receptor, Serotonin, 5-HT2C - metabolism; Serotonin Receptor Agonists - chemistry; Serotonin Receptor Agonists - pharmacology; Structure-Activity Relationship
• ISSN: 1554-8929; 1554-8937
• DOI: 10.1021/acschembio.5b01045

Agonism of the 5-HT2C serotonin receptor has been associated with the treatment of a number of diseases including obesity, psychiatric disorders, sexual health, and urology. However, the development of effective 5-HT2C agonists has been hampered by the difficulty in obtaining selectivity over the closely related 5-HT2B receptor, agonism of which is associated with irreversible cardiac valvulopathy. Understanding how to design selective agonists requires exploration of the structural features governing the functional uniqueness of the target receptor relative to related off targets. X-ray crystallography, the major experimental source of structural information, is a slow and challenging process for integral membrane proteins, and so is currently not feasible for every GPCR or GPCR–ligand complex. Therefore, the integration of existing ligand SAR data with GPCR modeling can be a practical alternative to provide this essential structural insight. To demonstrate this, we integrated SAR data from 39 azepine series 5-HT2C agonists, comprising both selective and unselective examples, with our hierarchical GPCR modeling protocol (HGMP). Through this work we have been able to demonstrate how relatively small differences in the amino acid sequences of GPCRs can lead to significant differences in secondary structure and function, as supported by experimental data. In particular, this study suggests that conformational differences in the tilt of TM7 between 5-HT2B and 5-HT2C, which result from differences in interhelical interactions, may be the major source of selectivity in G-protein activation between these two receptors. Our approach also demonstrates how the use of GPCR models in conjunction with SAR data can be used to explain activity cliffs.