The α-factor mating pheromone of Saccharomyces cerevisiae:: a model for studying the interaction of peptide hormones and G protein-coupled receptors

被引:68
作者
Naider, F [1 ]
Becker, JM
机构
[1] CUNY Coll Staten Isl, Dept Chem, Staten Isl, NY 10314 USA
[2] CUNY Coll Staten Isl, Inst Macromol Assemblies, Staten Isl, NY 10314 USA
[3] CUNY, Grad Sch, New York, NY 10016 USA
[4] CUNY, Univ Ctr, New York, NY 10016 USA
[5] Univ Tennessee, Dept Microbiol, Knoxville, TN 37996 USA
[6] Univ Tennessee, ORNL Grad Sch Genome Sci & Technol, Knoxville, TN 37996 USA
关键词
Saccharomyces cerevisiae; antagonists; G protein-coupled receptors; mating pheromone;
D O I
10.1016/j.peptides.2003.11.028
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:1441 / 1463
页数:23
相关论文
共 159 条
[1]   Mutations affecting ligand specificity of the G-protein-coupled receptor for the Saccharomyces cerevisiae tridecapeptide pheromone [J].
Abel, MG ;
Lee, BK ;
Naider, F ;
Becker, JM .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 1998, 1448 (01) :12-26
[2]  
Abel MG, 1998, J PEPT RES, V52, P95
[3]  
ALBERICIO F, 1991, INT J PEPT PROT RES, V37, P402
[4]   Scanning mutagenesis identifies amino acid side chains in transmembrane domain 5 of the M1 muscarinic receptor that participate in binding the acetyl methyl group of acetylcholine [J].
Allman, K ;
Page, KM ;
Curtis, CAM ;
Hulme, EC .
MOLECULAR PHARMACOLOGY, 2000, 58 (01) :175-184
[5]  
ANDEREGG RJ, 1988, J BIOL CHEM, V263, P18236
[6]  
Antohi O, 1998, BIOPOLYMERS, V45, P21, DOI 10.1002/(SICI)1097-0282(199801)45:1<21::AID-BIP3>3.0.CO
[7]  
2-0
[8]   Rhodopsin-transducin interface: Studies with conformationally constrained peptides [J].
Arimoto, R ;
Kisselev, OG ;
Makara, GM ;
Marshall, GR .
BIOPHYSICAL JOURNAL, 2001, 81 (06) :3285-3293
[9]   Property-based design of GPCR-targeted library [J].
Balakin, KV ;
Tkachenko, SE ;
Lang, SA ;
Okun, I ;
Ivashchenko, AA ;
Savchuk, NP .
JOURNAL OF CHEMICAL INFORMATION AND COMPUTER SCIENCES, 2002, 42 (06) :1332-1342
[10]   COMPLETE L-ALANINE SCAN OF NEUROPEPTIDE-Y REVEALS LIGANDS BINDING TO Y-1 AND Y-2 RECEPTORS WITH DISTINGUISHED CONFORMATIONS [J].
BECKSICKINGER, AG ;
WIELAND, HA ;
WITTNEBEN, H ;
WILLIM, KD ;
RUDOLF, K ;
JUNG, G .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1994, 225 (03) :947-958