Opioid receptor random mutagenesis reveals a mechanism for G protein-coupled receptor activation

被引:77
作者
Décaillot, FM
Befort, K
Filliol, D
Yue, SY
Walker, P
Kieffer, BL [1 ]
机构
[1] IGBMC, F-67404 Illkirch Graffenstaden, France
[2] AstraZeneca Res Ctr Montreal, Dept Chem, Montreal, PQ H4S 1Z9, Canada
[3] AstraZeneca Res Ctr Montreal, Dept Mol Biol, Montreal, PQ H4S 1Z9, Canada
关键词
D O I
10.1038/nsb950
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
The high resolution structure of rhodopsin has greatly enhanced current understanding of G protein coupled receptor ( GPCR) structure in the off-state, but the activation process remains to be clarified. We investigated molecular mechanisms of delta-opioid receptor activation without a preconceived structural hypothesis. Using random mutagenesis of the entire receptor, we identified 30 activating point mutations. Three-dimensional modeling revealed an activation path originating from the third extracellular loop and propagating through tightly packed helices III, VI and VII down to a VI-VII cytoplasmic switch. N- and C-terminal determinants also influence receptor activity. Findings for this therapeutically important receptor may apply to other GPCRs that respond to diffusible ligands.
引用
收藏
页码:629 / 636
页数:8
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