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Structure of class C GPCR metabotropic glutamate receptor 5 transmembrane domain
被引:327
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
来源:
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:
07 ;
0710 ;
09 ;
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.
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页码:557 / +
页数:18
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