A single serine residue confers tetrodotoxin insensitivity on the rat sensory-neuron-specific sodium channel SNS

被引:64
作者
Sivilotti, L
Okuse, K
Akopian, AN
Moss, S
Wood, JN
机构
[1] UCL, DEPT ANAT, LONDON WC1 8LS, ENGLAND
[2] UCL, DEPT DEV BIOL, LONDON WC1 8LS, ENGLAND
[3] UCL, MRC, MOL BIOL LAB, LONDON WC1 8LS, ENGLAND
[4] UCL, DEPT PHARMACOL, LONDON WC1 8LS, ENGLAND
基金
英国惠康基金;
关键词
dorsal root ganglion; tetrodotoxin; saxitoxin; mutagenesis; sodium channel;
D O I
10.1016/S0014-5793(97)00479-1
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
Sensory neurons express a sodium channel (SNS) that is highly resistant to block by tetrodotoxin (IC50 = 60 mu M). SNS is 65% homologous to the cardiac sodium channel, in which a single hydrophilic residue in the SS2 segment is critical for tetrodotoxin resistance, By site-directed mutagenesis, we have substituted phenylalanine for serine at the equivalent position in SNS: this mutated (S356E) SNS channel is functionally similar to wild-type SNS when expressed in Xenopus oocytes, but is potently blocked by tetrodotoxin and saxitoxin with IC(50)s of 2.8 nM and 8.2 nM, respectively, These data provide clues to the rational design of selective blockers of SNS with potential as analgesic drugs. (C) 1997 Federation of European Biochemical Societies.
引用
收藏
页码:49 / 52
页数:4
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