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Heptares Announces Publication In Nature Of Class B GPCR Structure
Unique structural insights from CRF1 structure will drive drug discovery programmes targeting important Class B GPCRs including GLP1 (diabetes)
Welwyn Garden City, UK and Boston, MA, USA, 17 July 2013 – Heptares Therapeutics, the leading GPCR drug discovery and development company, announces the publication of a scientific article describing the high resolution X-ray crystal structure of the corticotropin-releasing factor receptor 1 (CRF1) receptor. The paper has been published in Nature (ref. below) and is available online to subscribers by clicking here.
CRF1 is the receptor for the hormone CRF, which is important in regulating the body’s response to stress and is implicated in stress-related diseases such as depression and anxiety. It is a member of the Class B family of GPCRs, which includes receptors for peptide hormones such as glucagon, glucagon-like peptide, calcitonin and parathyroid peptide hormone. This important class of GPCRs includes drug targets for the treatment of various diseases, including diabetes, osteoporosis, depression and anxiety; however, to date it has proved intractable to small molecule drug discovery owing to the limited structural information available.
In this paper, the authors from Heptares describe novel insights into the topology of CRF1, and identify major differences compared to the many already known Class A GPCR structures. A unique aspect of the structure is the discovery of the binding pocket of the small molecule CRF1 antagonists near the cytoplasmic side of the receptor in a completely different position to other GPCR ligands.
Owing to the close relationship among Class B GPCRs, these insights from the CRF1 structure are enabling Heptares to generate high-quality structural models of other Class B GPCRs, providing new avenues for discovery, which are being leveraged by the Company using its proprietary structure-based drug design platform. Heptares is also developing programmes focused on Class B receptors involved in metabolic disease, including GLP1 and glucagon receptors (diabetes), and has the potential to apply its platform to other Class B GPCRs that have been clinically validated across multiple disease areas.
Fiona Marshall, Chief Scientific Officer at Heptares, commented: “The finding that the structure of CRF1, a Class B GPCR, is completely different to previously solved Class A receptors confirms why Class B receptors could not previously be modelled for the purpose of rational drug design. In demonstrating that our StaR® methodology can now be applied across both Class A and B GPCRs to enable structure determination, we have greatly enhanced our ability to carry out structure-based drug discovery for important GPCRs in both groups.”
Heptares would like to acknowledge the use of the Diamond Light Source, the UK’s national synchrotron science facility, and the help of their beamline scientists in the determination of the CRF1 structure.
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