Identification of a conserved ankyrin-binding motif in the family of sodium channel alpha subunits
UMass Chan Affiliations
Cell BiologyDocument Type
Journal ArticlePublication Date
2003-04-30Keywords
Amino Acid MotifsAmino Acid Sequence
Animals
Ankyrins
Cell Adhesion Molecules
Cell Line
Cell Membrane
Cells, Cultured
Cricetinae
DNA, Complementary
Hippocampus
Microscopy, Fluorescence
Molecular Sequence Data
Nerve Growth Factors
Neurons
Plasmids
Protein Binding
Protein Structure, Tertiary
Rats
Rats, Wistar
Recombinant Fusion Proteins
Sequence Homology, Amino Acid
Sodium Channels
Transfection
Two-Hybrid System Techniques
Life Sciences
Medicine and Health Sciences
Metadata
Show full item recordAbstract
Interactions with ankyrinG 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 ankyrinG 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 ankyrinG 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.Source
J Biol Chem. 2003 Jul 25;278(30):27333-9. Epub 2003 Apr 25. Link to article on publisher's siteDOI
10.1074/jbc.M303327200Permanent Link to this Item
http://hdl.handle.net/20.500.14038/42362PubMed ID
12716895Related Resources
Link to Article in PubMedae974a485f413a2113503eed53cd6c53
10.1074/jbc.M303327200