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 AbstractBiologically significant conformation of the Saccharomyces cerevisiae alpha-factor    Next AbstractDouble-mutant cycle scanning of the interaction of a peptide ligand and its G protein-coupled receptor »

Peptides


Title:The alpha-factor mating pheromone of Saccharomyces cerevisiae: a model for studying the interaction of peptide hormones and G protein-coupled receptors
Author(s):Naider F; Becker JM;
Address:"Department of Chemistry, College of Staten Island and Institute for Macromolecular Assemblies of The City University of New York, Staten Island, NY 10314, USA. naider@postbox.csi.cuny.edu"
Journal Title:Peptides
Year:2004
Volume:25
Issue:9
Page Number:1441 - 1463
DOI: 10.1016/j.peptides.2003.11.028
ISSN/ISBN:0196-9781 (Print) 0196-9781 (Linking)
Abstract:"Mating in Saccharomyces cerevisiae is initiated by the secretion of diffusible peptide pheromones that are recognized by G protein-coupled receptors (GPCR). This review summarizes the use of the alpha-factor (WHWLQLKPGQPMY)--GPCR (Ste2p) interaction as a paradigm to understand the recognition between medium-sized peptide hormones and their cognate receptors. Studies over the past 15 years have indicated that the alpha-factor is bent around the center of the pheromone and that residues near the amine terminus play a central role in triggering signal transduction. The bend in the center appears not to be rigid and this flexibility is likely necessary for conformational changes that occur as the receptor switches from the inactive to active state. The results of synthetic, biological, biochemical, molecular biological, and biophysical analyses have led to a preliminary model for the structure of the peptide bound to its receptor. Antagonists for Ste2p have changes near the N-terminus of alpha-factor, and mutated forms of Ste2p were discovered that appear to favor binding of these antagonists relative to agonists. Many features of this yeast recognition system are relevant to and have counterparts in mammalian cells"
Keywords:"Alanine/chemistry Binding Sites Binding, Competitive Dose-Response Relationship, Drug *Fungal Proteins *Genes, Fungal Glycosylation Iodine/chemistry Kinetics Ligands Light Models, Chemical Models, Molecular Mutation Peptide Hormones/*chemistry Peptides/ch;"
Notes:"MedlineNaider, Fred Becker, Jeffrey M eng GM22086/GM/NIGMS NIH HHS/ GM22087/GM/NIGMS NIH HHS/ Research Support, U.S. Gov't, P.H.S. Review 2004/09/18 Peptides. 2004 Sep; 25(9):1441-63. doi: 10.1016/j.peptides.2003.11.028"

 
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 28-11-2024