Structure of class C GPCR metabotropic glutamate receptor 5 transmembrane domain

被引:356
作者
Dore, Andrew S. [1 ]
Okrasa, Krzysztof [1 ]
Patel, Jayesh C. [1 ]
Serrano-Vega, Maria [1 ]
Bennett, Kirstie [1 ]
Cooke, Robert M. [1 ]
Errey, James C. [1 ]
Jazayeri, Ali [1 ]
Khan, Samir [1 ]
Tehan, Ben [1 ]
Weir, Malcolm [1 ]
Wiggin, Giselle R. [1 ]
Marshall, Fiona H. [1 ]
机构
[1] Heptares Therapeut Ltd, Welwyn Garden City AL7 3AX, Herts, England
关键词
PROTEIN-COUPLED RECEPTORS; ALLOSTERIC MODULATORS; HEPTAHELICAL DOMAIN; CRYSTAL-STRUCTURE; BINDING POCKETS; ACTIVATION; FAMILY; THERMOSTABILIZATION; ANTAGONISTS; MUTATIONS;
D O I
10.1038/nature13396
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
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Metabotropic glutamate receptors are class C G-protein-coupled receptors which respond to the neurotransmitter glutamate. Structural studies have been restricted to the amino-terminal extracellular domain, providing little understanding of the membrane-spanning signal transduction domain. Metabotropic glutamate receptor 5 is of considerable interest as a drug target in the treatment of fragile X syndrome, autism, depression, anxiety, addiction and movement disorders. Here we report the crystal structure of the transmembrane domain of the human receptor in complex with the negative allosteric modulator, mavoglurant. The structure provides detailed insight into the architecture of the transmembrane domain of class C receptors including the precise location of the allosteric binding site within the transmem-branedomain and key micro-switches which regulate receptor signalling. This structure also provides a model for all class CG-protein-coupled receptors and may aid in the design of new small-molecule drugs for the treatment of brain disorders.
引用
收藏
页码:557 / +
页数:18
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共 50 条
[1]
PHENIX: a comprehensive Python']Python-based system for macromolecular structure solution [J].
Adams, Paul D. ;
Afonine, Pavel V. ;
Bunkoczi, Gabor ;
Chen, Vincent B. ;
Davis, Ian W. ;
Echols, Nathaniel ;
Headd, Jeffrey J. ;
Hung, Li-Wei ;
Kapral, Gary J. ;
Grosse-Kunstleve, Ralf W. ;
McCoy, Airlie J. ;
Moriarty, Nigel W. ;
Oeffner, Robert ;
Read, Randy J. ;
Richardson, David C. ;
Richardson, Jane S. ;
Terwilliger, Thomas C. ;
Zwart, Peter H. .
ACTA CRYSTALLOGRAPHICA SECTION D-STRUCTURAL BIOLOGY, 2010, 66 :213-221
[2]
Ballesteros J. A., 1995, Neuroscience Methods, V25, P366, DOI [10.1016/S1043-9471(05)80049-7, DOI 10.1016/S1043-9471(05)80049-7, DOI 10.1016/S1043-9471]
[3]
Serine and threonine residues bend α-helices in the χ1 = g- conformation [J].
Ballesteros, JA ;
Deupi, X ;
Olivella, M ;
Haaksma, EEJ ;
Pardo, L .
BIOPHYSICAL JOURNAL, 2000, 79 (05) :2754-2760
[4]
Altered G-Protein Coupling in an mGluR6 Point Mutant Associated with Congenital Stationary Night Blindness [J].
Beqollari, Donald ;
Betzenhauser, Matthew J. ;
Kammermeier, Paul J. .
MOLECULAR PHARMACOLOGY, 2009, 76 (05) :992-997
[5]
Common structural requirements for heptahelical domain function in class A and class C G protein-coupled receptors [J].
Binet, Virginie ;
Duthey, Beatrice ;
Lecaillon, Jennifer ;
Vol, Claire ;
Quoyer, Julie ;
Labesse, Gilles ;
Pin, Jean-Philippe ;
Prezeau, Laurent .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (16) :12154-12163
[6]
Structure, pharmacology and therapeutic prospects of family C G-protein coupled receptors [J].
Brauner-Osborne, Hans ;
Wellendorph, Petrine ;
Jensen, Anders A. .
CURRENT DRUG TARGETS, 2007, 8 (01) :169-184
[7]
Crystallizing membrane proteins using lipidic mesophases [J].
Caffrey, Martin ;
Cherezov, Vadim .
NATURE PROTOCOLS, 2009, 4 (05) :706-731
[8]
Amino acids in the second and third intracellular loops of the parathyroid Ca2+-sensing receptor mediate efficient coupling to phospholipase C [J].
Chang, WH ;
Chen, TH ;
Pratt, S ;
Shoback, D .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (26) :19955-19963
[9]
MolProbity: all-atom structure validation for macromolecular crystallography [J].
Chen, Vincent B. ;
Arendall, W. Bryan, III ;
Headd, Jeffrey J. ;
Keedy, Daniel A. ;
Immormino, Robert M. ;
Kapral, Gary J. ;
Murray, Laura W. ;
Richardson, Jane S. ;
Richardson, David C. .
ACTA CRYSTALLOGRAPHICA SECTION D-STRUCTURAL BIOLOGY, 2010, 66 :12-21
[10]
Allosteric modulators of GPCRs: a novel approach for the treatment of CNS disorders [J].
Conn, P. Jeffrey ;
Christopoulos, Arthur ;
Lindsley, Craig W. .
NATURE REVIEWS DRUG DISCOVERY, 2009, 8 (01) :41-54