Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractCryptococcus neoformans mediator protein Ssn8 negatively regulates diverse physiological processes and is required for virulence    Next Abstract[Analysis of volatile constituents from leaves of plants by gas chromatography/mass spectrometry with solid-phase microextraction] »

J Biol Chem


Title:Activation of family C G-protein-coupled receptors by the tripeptide glutathione
Author(s):Wang M; Yao Y; Kuang D; Hampson DR;
Address:"Department of Pharmaceutical Sciences, University of Toronto, Toronto, Ontario M5S 2S2, Canada"
Journal Title:J Biol Chem
Year:2006
Volume:20060202
Issue:13
Page Number:8864 - 8870
DOI: 10.1074/jbc.M512865200
ISSN/ISBN:0021-9258 (Print) 0021-9258 (Linking)
Abstract:"The Family C G-protein-coupled receptors include the metabotropic glutamate receptors, the gamma-aminobutyric acid, type B (GABAB) receptor, the calcium-sensing receptor (CaSR), which participates in the regulation of calcium homeostasis in the body, and a diverse group of sensory receptors that encompass the amino acid-activated fish 5.24 chemosensory receptor, the mammalian T1R taste receptors, and the V2R pheromone receptors. A common feature of Family C receptors is the presence of an amino acid binding site. In this study, a preliminary in silico analysis of the size and shape of the amino acid binding pocket in selected Family C receptors suggested that some members of this family could accommodate larger ligands such as peptides. Subsequent screening and docking experiments identified GSH as a potential ligand or co-ligand at the fish 5.24 receptor and the rat CaSR. These in silico predictions were confirmed using an [3H]GSH radioligand binding assay and a fluorescence-based functional assay performed on wild-type and chimeric receptors. Glutathione was shown to act as an orthosteric agonist at the 5.24 receptor and as a potent enhancer of calcium-induced activation of the CaSR. Within the mammalian receptors, this effect was specific to the CaSR because GSH neither directly activated nor potentiated other Family C receptors including GPRC6A (the putative mammalian homolog of the fish 5.24 receptor), the metabotropic glutamate receptors, or the GABAB receptor. Our findings reveal a potential new role for GSH and suggest that this peptide may act as an endogenous modulator of the CaSR in the parathyroid gland where this receptor is known to control the release of parathyroid hormone, and in other tissues such as the brain and gastrointestinal tract where the role of the calcium receptor appears to subserve other, as yet unknown, physiological functions"
Keywords:"Animals Calcium/metabolism Cell Line Dose-Response Relationship, Drug Fishes Fluorescence Glutathione/*metabolism/pharmacology Humans Immunoblotting Ligands Models, Molecular Phenylalanine/metabolism Radioligand Assay Rats Receptors, Calcium-Sensing/*meta;"
Notes:"MedlineWang, Minghua Yao, Yi Kuang, Donghui Hampson, David R eng Comparative Study Research Support, Non-U.S. Gov't 2006/02/04 J Biol Chem. 2006 Mar 31; 281(13):8864-70. doi: 10.1074/jbc.M512865200. Epub 2006 Feb 2"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 25-11-2024