Cyclotides isolated from an ipecac root extract antagonize the corticotropin releasing factor type 1 receptor

Fahradpour, Mohsen, Keov, Peter, Tognola, Carlotta, Perez-Santamarina, Estela, McCormick, Peter J., Ghassempour, Alireza and Gruber, Christian W. (2017) Cyclotides isolated from an ipecac root extract antagonize the corticotropin releasing factor type 1 receptor. Frontiers in Pharmacology, 8. ISSN 1663-9812

[thumbnail of Published manuscript]
Preview
PDF (Published manuscript) - Published Version
Available under License Creative Commons Attribution.

Download (4MB) | Preview

Abstract

Cyclotides are plant derived, cystine-knot stabilized peptides characterized by their natural abundance, sequence variability and structural plasticity. They are abundantly expressed in Rubiaceae, Psychotrieae in particular. Previously the cyclotide kalata B7 was identified to modulate the human oxytocin and vasopressin G protein-coupled receptors (GPCRs), providing molecular validation of the plants’ uterotonic properties and further establishing cyclotides as valuable source for GPCR ligand design. In this study we screened a cyclotide extract derived from the root powder of the South American medicinal plant ipecac (Carapichea ipecacuanha) for its GPCR modulating activity of the corticotropin-releasing factor type 1 receptor (CRF1R). We identified and characterized seven novel cyclotides. One cyclotide, caripe 8, isolated from the most active fraction, was further analyzed and found to antagonize the CRF1R. A nanomolar concentration of this cyclotide (260 nM) reduced CRF potency by ∼4.5-fold. In contrast, caripe 8 did not inhibit forskolin-, or vasopressin-stimulated cAMP responses at the vasopressin V2 receptor, suggesting a CRF1R-specific mode-of-action. These results in conjunction with our previous findings establish cyclotides as modulators of both classes A and B GPCRs. Given the diversity of cyclotides, our data point to other cyclotide-GPCR interactions as potentially important sources of drug-like molecules.

Item Type: Article
Uncontrolled Keywords: plant peptides,circular peptide,pharmacognosy,ipecac,gpcr,corticotropin-releasing factor
Faculty \ School: Faculty of Science > School of Biological Sciences
Faculty of Science > School of Pharmacy
Related URLs:
Depositing User: Pure Connector
Date Deposited: 14 Oct 2017 05:06
Last Modified: 04 Aug 2023 10:30
URI: https://ueaeprints.uea.ac.uk/id/eprint/65133
DOI: 10.3389/fphar.2017.00616

Downloads

Downloads per month over past year

Actions (login required)

View Item View Item