Molecular basis for convergent evolution of glutamate recognition by pentameric ligand-gated ion channels

被引:18
|
作者
Lynagh, Timothy [1 ]
Beech, Robin N. [2 ]
Lalande, Maryline J. [1 ]
Keller, Kevin [1 ]
Cromer, Brett A. [3 ]
Wolstenholme, Adrian J. [4 ,5 ]
Laube, Bodo [1 ]
机构
[1] Tech Univ Darmstadt, D-64287 Darmstadt, Germany
[2] McGill Univ, Inst Parasitol, Ste Anne De Bellevue, PQ, Canada
[3] RMIT Univ, Sch Med Sci, Hlth Innovat Res Inst, Bundoora, Vic, Australia
[4] Univ Georgia, Dept Infect Dis, Athens, GA 30602 USA
[5] Univ Georgia, Ctr Trop & Emerging Global Dis, Athens, GA 30602 USA
来源
SCIENTIFIC REPORTS | 2015年 / 5卷
关键词
PI BINDING INTERACTION; CHLORIDE CHANNEL; HAEMONCHUS-CONTORTUS; GABA RECEPTOR; RESIDUES CONTRIBUTE; GLYCINE RECEPTOR; BETA-SUBUNIT; AGONIST; SITE; ACTIVATION;
D O I
10.1038/srep08558
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
Glutamate is an indispensable neurotransmitter, triggering postsynaptic signals upon recognition by postsynaptic receptors. We questioned the phylogenetic position and the molecular details of when and where glutamate recognition arose in the glutamate-gated chloride channels. Experiments revealed that glutamate recognition requires an arginine residue in the base of the binding site, which originated at least three distinct times according to phylogenetic analysis. Most remarkably, the arginine emerged on the principal face of the binding site in the Lophotrochozoan lineage, but 65 amino acids upstream, on the complementary face, in the Ecdysozoan lineage. This combined experimental and computational approach throws new light on the evolution of synaptic signalling.
引用
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页数:8
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