International union of basic and clinical pharmacology. LXVII. Recommendations for the recognition and nomenclature of g protein-coupled receptor heteromultimers

被引:218
作者
Pin, Jean-Philippe
Neubig, Richard
Bouvier, Michel
Devi, Lakshmi
Filizola, Marta
Javitch, Jonathan A.
Lohse, Martin J.
Milligan, Graeme
Palczewski, Krzysztof
Parmentier, Marc
Spedding, Michael
机构
[1] Univ Montpellier I, CNRS UMR 5203, Inst Genom Fonct, INSERM U 661, F-34094 Montpellier 5, France
[2] Univ Montpellier 2, F-34095 Montpellier 5, France
[3] Univ Michigan, Sch Med, Dept Pharmacol, Ann Arbor, MI 48109 USA
[4] Univ Montreal, Inst Rech & Immunol & Cancerol, Unite Rech Pharmacol Mol, Montreal, PQ H3C 3J7, Canada
[5] CUNY Mt Sinai Sch Med, Dept Pharmacol & Biol Chem, New York, NY 10029 USA
[6] Cornell Univ, Weill Med Coll, Dept Physiol & Biophys, Ithaca, NY 14853 USA
[7] Columbia Univ, Coll Phys & Surg, Ctr Mol Recognit, New York, NY 10027 USA
[8] Columbia Univ, Coll Phys & Surg, Dept Psychiat, New York, NY 10027 USA
[9] Columbia Univ, Coll Phys & Surg, Dept Pharmacol, New York, NY 10027 USA
[10] Univ Wurzburg, Dept Pharmacol & Toxicol, D-97070 Wurzburg, Germany
[11] Univ Glasgow, Inst Biomed & Life Sci, Div Biochem & Pharmacol, Mol Pharmacol Grp, Glasgow G12 8QQ, Lanark, Scotland
[12] Case Western Reserve Univ, Sch Med, Dept Pharmacol, Cleveland, OH 44106 USA
[13] Univ Libre Bruxelles, Inst Rech Interdisciplinaire Biol Humaine & Mol, Brussels, Belgium
[14] Inst Res Servier, Suresnes, France
关键词
GABA(B) RECEPTOR; LIGAND-BINDING; ALPHA(1)-ADRENOCEPTOR SUBTYPES; CONFORMATIONAL-CHANGES; OLIGOMERIC STRUCTURE; HORMONE-RECEPTORS; FUNCTIONAL ROLES; OPIOID RECEPTORS; MAMMALIAN SWEET; AT1; RECEPTOR;
D O I
10.1124/pr.59.1.5
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
G protein-coupled receptors (GPCRs) have long been considered to be monomeric membrane proteins. Although numerous recent studies have indicated that GPCRs can form multimeric complexes, the functional and pharmacological consequences of this phenomenon have remained elusive. With the discovery that the functional GABA(B) receptor is an obligate heterodimer and with the use of energy transfer technologies, it is now accepted that GPCRs can form heteromultimers. In some cases, specific properties of such heteromers not shared by their respective homomers have been reported. Although in most cases these properties have only been observed in heterologous expression systems, there are a few reports describing data consistent with such heteromultimeric GPCR complexes also existing in native tissues. The present article illustrates well-documented examples of such native multimeric complexes, lists a number of recommendations for recognition and acceptance of such multimeric receptors, and gives recommendations for their nomenclature.
引用
收藏
页码:5 / 13
页数:9
相关论文
共 88 条
[11]   Monomeric G-protein-coupled receptor as a functional unit [J].
Chabre, M ;
le Maire, M .
BIOCHEMISTRY, 2005, 44 (27) :9395-9403
[12]   Detection of sweet and umami taste in the absence of taste receptor T1r3 [J].
Damak, S ;
Rong, MQ ;
Yasumatsu, K ;
Kokrashvili, Z ;
Varadarajan, V ;
Zou, SY ;
Jiang, PH ;
Ninomiya, Y ;
Margolskee, RF .
SCIENCE, 2003, 301 (5634) :850-853
[13]   Asymmetric conformational changes in a GPCR dimer controlled by G-proteins [J].
Damian, Marjorie ;
Martin, Aimee ;
Mesnier, Danielle ;
Pin, Jean-Philippe ;
Baneres, Jean-Louis .
EMBO JOURNAL, 2006, 25 (24) :5693-5702
[14]   Opioid-induced tolerance and dependence in mice is modulated by the distance between pharmacophores in a bivalent ligand series [J].
Daniels, DJ ;
Lenard, NR ;
Etienne, CL ;
Law, PY ;
Roerig, SC ;
Portoghese, PS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (52) :19208-19213
[15]   A bivalent ligand (KDAN-18) containing δ-antagonist and k-agonist pharmacophores bridges δ2 and k1 opioid receptor phenotypes [J].
Daniels, DJ ;
Kulkarni, A ;
Xie, ZH ;
Bhushan, RG ;
Portoghese, PS .
JOURNAL OF MEDICINAL CHEMISTRY, 2005, 48 (06) :1713-1716
[16]   Insights into the functional roles of α1-adrenoceptor subtypes in mouse carotid arteries using knockout mice [J].
Deighan, C ;
Methven, L ;
Naghadeh, MM ;
Wokoma, A ;
Macmillan, J ;
Daly, CJ ;
Tanoue, A ;
Tsujimoto, G ;
McGrath, JC .
BRITISH JOURNAL OF PHARMACOLOGY, 2005, 144 (04) :558-565
[17]   A single subunit (GB2) is required for G-protein activation by the heterodimeric GABAB receptor [J].
Duthey, B ;
Caudron, S ;
Perroy, J ;
Bettler, B ;
Fagni, L ;
Pin, JP ;
Prézeau, L .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (05) :3236-3241
[18]   Evidence for negative binding cooperativity within CCR5-CCR2b heterodimers [J].
El-Asmar, L ;
Springael, JY ;
Ballet, S ;
Andrieu, EU ;
Vassart, G ;
Parmentier, M .
MOLECULAR PHARMACOLOGY, 2005, 67 (02) :460-469
[19]   EGF activates its receptor by removing interactions that autoinhibit ectodomain dimerization [J].
Ferguson, KM ;
Berger, MB ;
Mendrola, JM ;
Cho, HS ;
Leahy, DJ ;
Lemmon, MA .
MOLECULAR CELL, 2003, 11 (02) :507-517
[20]   A concept for G protein activation by G protein-coupled receptor dimers: the transducin/rhodopsin interface [J].
Filipek, S ;
Krzysko, KA ;
Fotiadis, D ;
Liang, Y ;
Saperstein, DA ;
Engel, A ;
Palczewski, K .
PHOTOCHEMICAL & PHOTOBIOLOGICAL SCIENCES, 2004, 3 (06) :628-638