The structure and function of G-protein-coupled receptors

被引:1752
作者
Rosenbaum, Daniel M. [1 ]
Rasmussen, Soren G. F. [1 ]
Kobilka, Brian K. [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Cellular & Mol Physiol, Palo Alto, CA 94305 USA
关键词
BETA-ADRENERGIC-RECEPTOR; INTERNAL WATER-MOLECULES; CONSERVED ASPARTIC-ACID; CRYSTAL-STRUCTURE; BETA(2)-ADRENERGIC RECEPTOR; BOVINE RHODOPSIN; DRUG DISCOVERY; HELIX MOVEMENT; BINDING-SITE; IONIC LOCK;
D O I
10.1038/nature08144
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
G-protein-coupled receptors (GPCRs) mediate most of our physiological responses to hormones, neurotransmitters and environmental stimulants, and so have great potential as therapeutic targets for a broad spectrum of diseases. They are also fascinating molecules from the perspective of membrane-protein structure and biology. Great progress has been made over the past three decades in understanding diverse GPCRs, from pharmacology to functional characterization in vivo. Recent high-resolution structural studies have provided insights into the molecular mechanisms of GPCR activation and constitutive activity.
引用
收藏
页码:356 / 363
页数:8
相关论文
共 71 条
  • [1] Helix movement is coupled to displacement of the second extracellular loop in rhodopsin activation
    Ahuja, Shivani
    Hornak, Viktor
    Yan, Elsa C. Y.
    Syrett, Natalie
    Goncalves, Joseph A.
    Hirshfeld, Amiram
    Ziliox, Martine
    Sakmar, Thomas P.
    Sheves, Mordechai
    Reeves, Philip J.
    Smith, Steven O.
    Eilers, Markus
    [J]. NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2009, 16 (02) : 168 - 175
  • [2] High-resolution distance mapping in rhodopsin reveals the pattern of helix movement due to activation
    Altenbach, Christian
    Kusnetzow, Ana Karin
    Ernst, Oliver P.
    Hofmann, Klaus Peter
    Hubbell, Wayne L.
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (21) : 7439 - 7444
  • [3] β-Arrestin-mediated activation of MAPK by inverse agonists reveals distinct active conformations for G protein-coupled receptors
    Azzi, M
    Charest, PG
    Angers, S
    Rousseau, G
    Kohout, T
    Bouvier, M
    Piñeyro, G
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (20) : 11406 - 11411
  • [4] The selectivity of β-adrenoceptor antagonists at the human β1, β2 and β3 adrenoceptors
    Baker, JG
    [J]. BRITISH JOURNAL OF PHARMACOLOGY, 2005, 144 (03) : 317 - 322
  • [5] Ballesteros J. A., 1995, METH NEUROSCI, P366, DOI [DOI 10.1016/S1043-9471, DOI 10.1016/S1043-9471(05)80049-7]
  • [6] Activation of the β2-adrenergic receptor involves disruption of an ionic lock between the cytoplasmic ends of transmembrane segments 3 and 6
    Ballesteros, JA
    Jensen, AD
    Liapakis, G
    Rasmussen, SGF
    Shi, L
    Gether, U
    Javitch, JA
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (31) : 29171 - 29177
  • [7] THE CONSERVED 7-TRANSMEMBRANE SEQUENCE NP(X)(2,3)Y OF THE G-PROTEIN-COUPLED RECEPTOR SUPERFAMILY REGULATES MULTIPLE PROPERTIES OF THE BETA(2)-ADRENERGIC RECEPTOR
    BARAK, LS
    MENARD, L
    FERGUSON, SSG
    COLAPIETRO, AM
    CARON, MG
    [J]. BIOCHEMISTRY, 1995, 34 (47) : 15407 - 15414
  • [8] Recent developments in constitutive receptor activity and inverse agonism, and their potential for GPCR drug discovery
    Bond, RA
    IJzerman, AP
    [J]. TRENDS IN PHARMACOLOGICAL SCIENCES, 2006, 27 (02) : 92 - 96
  • [9] Crystallizing Membrane Proteins for Structure Determination: Use of Lipidic Mesophases
    Caffrey, Martin
    [J]. ANNUAL REVIEW OF BIOPHYSICS, 2009, 38 : 29 - 51
  • [10] High-resolution crystal structure of an engineered human β2-adrenergic G protein-coupled receptor
    Cherezov, Vadim
    Rosenbaum, Daniel M.
    Hanson, Michael A.
    Rasmussen, Soren G. F.
    Thian, Foon Sun
    Kobilka, Tong Sun
    Choi, Hee-Jung
    Kuhn, Peter
    Weis, William I.
    Kobilka, Brian K.
    Stevens, Raymond C.
    [J]. SCIENCE, 2007, 318 (5854) : 1258 - 1265