Activation of G Protein Coupled Receptors

被引:68
作者
Deupi, Xavier [1 ]
Kobilka, Brian [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Cellular & Mol Physiol, Stanford, CA 94305 USA
来源
MECHANISMS AND PATHWAYS OF HETEROTRIMERIC G PROTEIN SIGNALING | 2007年 / 74卷
关键词
D O I
10.1016/S0065-3231(07)74004-4
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
G protein-coupled receptors (GPCRs) mediate responses to hormones and neurotransmitters, as well as the senses of sight, smell, and taste. These remarkably versatile signaling molecules respond to structurally diverse ligands. Many GPCRs couple to multiple G protein subtypes, and several have been shown to activate G protein-independent signaling pathways. Drugs acting on GPCRs exhibit efficacy profiles that may differ for different signaling cascades. The functional plasticity exhibited by GPCRs can be attributed to structural flexibility and the existence of multiple ligand-specific conformational states. This chapter will review our current understanding of the mechanism by which agonists bind and activate GPCRs.
引用
收藏
页码:137 / 166
页数:30
相关论文
共 104 条
[31]  
Hubbell WL, 2003, ADV PROTEIN CHEM, V63, P243
[32]   The ants go marching two by two: Oligomeric structure of G-protein-coupled receptors [J].
Javitch, JA .
MOLECULAR PHARMACOLOGY, 2004, 66 (05) :1077-1082
[33]   Constitutive activation of the beta(2) adrenergic receptor alters the orientation of its sixth membrane-spanning segment [J].
Javitch, JA ;
Fu, DY ;
Liapakis, G ;
Chen, JY .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (30) :18546-18549
[34]   Agonist-induced conformational changes at the cytoplasmic side of transmembrane segment 6 in the β2 adrenergic receptor mapped by site-selective fluorescent labeling [J].
Jensen, AD ;
Guarnieri, F ;
Rasmussen, SGF ;
Asmar, F ;
Ballesteros, JA ;
Gether, U .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (12) :9279-9290
[35]   G protein-coupled receptors I. Diversity of receptor-ligand interactions [J].
Ji, TH ;
Grossmann, M ;
Ji, IH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (28) :17299-17302
[36]   Linking agonist binding to histamine H1 receptor activation [J].
Jongejan, A ;
Bruysters, M ;
Ballesteros, JA ;
Haaksma, E ;
Bakker, RA ;
Pardo, L ;
Leurs, R .
NATURE CHEMICAL BIOLOGY, 2005, 1 (02) :98-103
[37]   Inverse, protean, and ligand-selective agonism: matters of receptor conformation [J].
Kenakin, T .
FASEB JOURNAL, 2001, 15 (03) :598-611
[38]   Efficacy at G-protein-coupled receptors [J].
Kenakin, T .
NATURE REVIEWS DRUG DISCOVERY, 2002, 1 (02) :103-110
[39]   Ligand-selective receptor conformations revisited: the promise and the problem [J].
Kenakin, T .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2003, 24 (07) :346-354
[40]   Structure and function in rhodopsin: Rhodopsin mutants with a neutral amino acid at E134 have a partially activated conformation in the dark state [J].
Kim, JM ;
Altenbach, C ;
Thurmond, RL ;
Khorana, HG ;
Hubbell, WL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (26) :14273-14278