Identification of a conserved ankyrin-binding motif in the family of sodium channel α Subunits

被引:192
作者
Lemaillet, G
Walker, B
Lambert, S
机构
[1] Univ Massachusetts, Sch Med, Dept Cell Biol, Worcester, MA 01605 USA
[2] Univ Massachusetts, Sch Med, Program Neurosci, Worcester, MA 01605 USA
关键词
D O I
10.1074/jbc.M303327200
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
Interactions with ankyrin(G) are crucial to the localization of voltage-gated sodium channels (VGSCs) at the axon initial segment and for neurons to initiate action potentials. However, the molecular nature of these interactions remains unclear. Here we report that VGSC-alpha, but not -beta, subunits bind to ankyrin(G) using pull-down assays. Further dissection of this activity identifies a conserved 9-amino acid motif ((V/A) P(I/L) AXXE(S/D)D) required for ankyrin(G) binding. This motif is also required for the localization of chimeric neurofascin/sodium channel molecules to the initial segment of cultured hippocampal neurons. The conserved nature of this motif suggests that it functions to localize sodium channels to a variety of "excitable" membrane domains both inside and outside of the nervous system.
引用
收藏
页码:27333 / 27339
页数:7
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