Structural and Functional Insights into CRF Peptides and Their Receptors

Author:

Matsoukas Minos-Timotheos1,Panagiotopoulos Vasilis1ORCID,Karageorgos Vlasios2,Chrousos George P.3ORCID,Venihaki Maria4ORCID,Liapakis George2ORCID

Affiliation:

1. Department of Biomedical Engineering, School of Engineering, University of West Attica, 12243 Athens, Greece

2. Department of Pharmacology, Faculty of Medicine, University of Crete, 71003 Heraklion, Greece

3. University Research Institute of Maternal and Child Health and Precision Medicine and UNESCO, National and Kapodistrian University of Athens, Livadias 8, 11527 Athens, Greece

4. Department of Clinical Chemistry, Faculty of Medicine, University of Crete, 71003 Heraklion, Greece

Abstract

Corticotropin-releasing factor or hormone (CRF or CRH) and the urocortins regulate a plethora of physiological functions and are involved in many pathophysiological processes. CRF and urocortins belong to the family of CRF peptides (CRF family), which includes sauvagine, urotensin, and many synthetic peptide and non-peptide CRF analogs. Several of the CRF analogs have shown considerable therapeutic potential in the treatment of various diseases. The CRF peptide family act by interacting with two types of plasma membrane proteins, type 1 (CRF1R) and type 2 (CRF2R), which belong to subfamily B1 of the family B G-protein-coupled receptors (GPCRs). This work describes the structure of CRF peptides and their receptors and the activation mechanism of the latter, which is compared with that of other GPCRs. It also discusses recent structural information that rationalizes the selective binding of various ligands to the two CRF receptor types and the activation of receptors by different agonists.

Funder

University of Crete

Publisher

MDPI AG

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