MOLECULAR-BASIS OF MUSCARINIC ACETYLCHOLINE-RECEPTOR FUNCTION

被引:173
作者
WESS, J
机构
[1] J. Wess is a Principal Investigator at the National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Laboratory of Bio-organic Chemistry, Bidg 8A, Rm B1A-09. Bethesda
关键词
D O I
10.1016/0165-6147(93)90049-P
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Muscarinic acetylcholine receptors play important roles in numerous physiological functions including higher cognitive processes such as memory and learning. Consistent with the well-documented pharmacological heterogeneity of muscarinic receptors, molecular cloning studies have revealed the existence of five distinct muscarinic receptor proteins (M1-M5). Structure-function relationship studies of the cloned receptors have been greatly aided by the high degree of structural homology that muscarinic receptors share with other G protein-coupled receptors. In this review, Jurgen Wess discusses recent mutagenesis studies that have considerably advanced our knowledge of the molecular details underlying muscarinic receptor function.
引用
收藏
页码:308 / 313
页数:6
相关论文
共 45 条
[1]   MUTATIONAL ANALYSIS OF 3RD CYTOPLASMIC LOOP DOMAINS IN G-PROTEIN COUPLING OF THE HM1 MUSCARINIC RECEPTOR [J].
ARDEN, JR ;
NAGATA, O ;
SHOCKLEY, MS ;
PHILIP, M ;
LAMEH, J ;
SADEE, W .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1992, 188 (03) :1111-1115
[2]  
BERSTEIN G, 1992, J BIOL CHEM, V267, P8081
[3]  
Birdsall N. J. M., 1993, Life Sciences, V52, P561, DOI 10.1016/0024-3205(93)90338-4
[4]   THE MOLECULAR-BASIS OF MUSCARINIC RECEPTOR DIVERSITY [J].
BONNER, TI .
TRENDS IN NEUROSCIENCES, 1989, 12 (04) :148-151
[5]  
CHEUNG AH, 1992, MOL PHARMACOL, V41, P1061
[6]  
CURTIS CAM, 1989, J BIOL CHEM, V264, P489
[7]   MODEL SYSTEMS FOR THE STUDY OF 7-TRANSMEMBRANE-SEGMENT RECEPTORS [J].
DOHLMAN, HG ;
THORNER, J ;
CARON, MG ;
LEFKOWITZ, RJ .
ANNUAL REVIEW OF BIOCHEMISTRY, 1991, 60 :653-688
[8]  
FRASER CM, 1989, MOL PHARMACOL, V36, P840
[9]   SITE-DIRECTED MUTAGENESIS OF HUMAN BETA-ADRENERGIC RECEPTORS - SUBSTITUTION OF ASPARTIC ACID-130 BY ASPARAGINE PRODUCES A RECEPTOR WITH HIGH-AFFINITY AGONIST BINDING THAT IS UNCOUPLED FROM ADENYLATE-CYCLASE [J].
FRASER, CM ;
CHUNG, FZ ;
WANG, CD ;
VENTER, JC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (15) :5478-5482
[10]   MODEL FOR THE STRUCTURE OF BACTERIORHODOPSIN BASED ON HIGH-RESOLUTION ELECTRON CRYOMICROSCOPY [J].
HENDERSON, R ;
BALDWIN, JM ;
CESKA, TA ;
ZEMLIN, F ;
BECKMANN, E ;
DOWNING, KH .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 213 (04) :899-929