TY - JOUR
T1 - Caenorhabditis elegans degenerins and vertebrate ENaC ion channels contain an extracellular domain related to venom neurotoxins
AU - Tavernarakis, Nektarios
AU - Driscoll, Monica
N1 - Funding Information:
Research was supported by grants from the National Science Foundation (IBN-9511710) and National Institutes of Health (NS34435, NS37955). M.D. is a fellow of the Alfred P. Sloan Foundation, N.T. is supported by Human Frontiers in Science Program Organization Research Fellowship.
PY - 2000
Y1 - 2000
N2 - The DEG/ENaC (DEGenerin/Epithelial Na+ Channel) superfamily includes closely related ion channel subunits from divergent species ranging from the simple nematode Caenorhabditis elegans to humans. Members of this protein group play roles in several important processes including transduction of mechanical stimuli, sodium re-absorption and blood pressure regulation. Structure/function relationships in members of this superfamily are just beginning to be elaborated. Using a bioinformatics approach, we identified a novel structural element in the extracellular region of DEG/ENaC proteins that exhibits significant similarity to venom neurotoxins. Since venom neurotoxins bind to sodium channels at high affinity, we suggest that the related domain embedded in DEG/ENaC channels may interact with other regions of the channel or channel complex to modulate channel function.
AB - The DEG/ENaC (DEGenerin/Epithelial Na+ Channel) superfamily includes closely related ion channel subunits from divergent species ranging from the simple nematode Caenorhabditis elegans to humans. Members of this protein group play roles in several important processes including transduction of mechanical stimuli, sodium re-absorption and blood pressure regulation. Structure/function relationships in members of this superfamily are just beginning to be elaborated. Using a bioinformatics approach, we identified a novel structural element in the extracellular region of DEG/ENaC proteins that exhibits significant similarity to venom neurotoxins. Since venom neurotoxins bind to sodium channels at high affinity, we suggest that the related domain embedded in DEG/ENaC channels may interact with other regions of the channel or channel complex to modulate channel function.
KW - Anti-epilepsy peptide
KW - Kunitz-type protease inhibitors
KW - Mechanotransduction
KW - Neurodegeneration
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U2 - 10.3109/01677060009084497
DO - 10.3109/01677060009084497
M3 - Article
C2 - 10858823
AN - SCOPUS:0034090625
SN - 0167-7063
VL - 13
SP - 257
EP - 264
JO - Journal of Neurogenetics
JF - Journal of Neurogenetics
IS - 4
ER -