Mapping the receptor site for ergtoxin, a specific blocker of ERG channels

被引:29
作者
Pardo-López, L
Garcia-Valdés, J
Gurrola, GB
Robertson, GA
Possani, LD
机构
[1] Univ Nacl Autonoma Mexico, Inst Biotechnol, Dept Mol Recognit & Sturct Biol, Cuernavaca 62210, Morelos, Mexico
[2] Univ Wisconsin, Sch Med, Dept Physiol, Madison, WI 53706 USA
来源
FEBS LETTERS | 2002年 / 510卷 / 1-2期
关键词
human ether-a-go-go-related gene channel; K+; channel; ergtoxin; M-elk channel; M-eag channel; scorpion toxin;
D O I
10.1016/S0014-5793(01)03218-5
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
We show here that ergtoxin (ErgTx) is a bona ride, specific blocker of the human ether-a-go-go-related gene (HERG) channels. It does not affect the function of either M-eag or M-elk channels. A chimeric construction containing a segment of the P-region of M-eag channel inserted into the HERG channel drastically diminished or completely abolished the inhibitory effect of ErgTx, whereas chimeras of the P-region of HERG channel into M-eag channels recovered the inhibitory effect. From the P-region point mutants of HERG channel assays, only the mutant N598Q shows about 25% decrement of the ErgTx inhibitory effect. ErgTx recognizes the P-region of HERG channels, blocking the channel function with a K-d in the order of 12 nM. (C) 2002 Published by Elsevier Science B.V. on behalf of the Federation of European Biochemical Societies.
引用
收藏
页码:45 / 49
页数:5
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