Specific interactions between the syntrophin PDZ domain and voltage-gated sodium channels

被引:190
作者
Schultz, J
Hoffmüller, U
Krause, G
Ashurst, J
Macias, MJ
Schmieder, P
Schneider-Mergener, J
Oschkinat, H
机构
[1] Forschungsinst Mol Pharmakol, D-10315 Berlin, Germany
[2] Humboldt Univ, Klinikum Charite, Inst Med Immunol, D-10098 Berlin, Germany
[3] European Mol Biol Lab, D-69012 Heidelberg, Germany
关键词
D O I
10.1038/nsb0198-19
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
Syntrophins are modular proteins belonging to the dystrophin associated glycoprotein complex and are thought to be involved in the regulation of the muscular system. Screening of peptide libraries revealed selectivity of the synotrophin PDZ domain toward the motif R/K/Q-E-S/T-X-V-COO- found to be highly conserved in the alpha-subunit C-terminus of vertebrate voltage gated sodium channels (VGSCs). The solution structure of the domain in complex with the peptide G-V-K-E-S-L-V shows specific interactions between the conserved residues in the peptide and syntrophin-characteristic residues of the domain. We propose that syntrophins localize VGSCs to the dystrophin network through its PDZ domain.
引用
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页码:19 / 24
页数:6
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