Open AccessInsights into the Molecular Determinants Involved in Urocontrin and Urocontrin A Action
Author(s) -
Étienne Billard,
David Chatenet
Publication year - 2020
Publication title -
acs medicinal chemistry letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.065
H-Index - 66
ISSN - 1948-5875
DOI - 10.1021/acsmedchemlett.0c00223
Subject(s) - allosteric regulation , computational biology , residue (chemistry) , function (biology) , peptide , chemistry , stereochemistry , computer science , biochemistry , biology , microbiology and biotechnology , receptor
In the past few years, we have identified two allosteric modulators of the urotensinergic system with probe-dependent action, termed Urocontrin (UC) and Urocontrin A (UCA). Such action is atypical and important since it will allow us to understand the specific function of the functionally selective cognate ligands of this system, namely urotensin II and urotensin II-related peptide. Delineating the molecular determinants involved in this particular behavior would represent an important step toward designing small molecules suitable for pharmacologic and/or therapeutic intervention. Hence, we undertook an exploratory research by replacing the Trp 4 residue of URP with several para-substituted phenylalanine amino acids in order to get a grasp on the required nature, distance, and orientation of the side chain of this residue for allosteric modulatory action. We found that the position of the second aromatic group is crucial, and we identified two new allosteric modulators: [Trip 4 ]URP and [Phe(pPy-4) 4 ]URP with probe-dependent action.