Gonoi T, Hille B, Catterall W A
J Neurosci. 1984 Nov;4(11):2836-42. doi: 10.1523/JNEUROSCI.04-11-02836.1984.
Sodium currents mediated by voltage-sensitive sodium channels in normal and scorpion toxin-resistant neuroblastoma cells were measured using a giga-ohm seal recording method in the whole cell patch configuration. The voltage and time dependence of sodium currents were similar in normal and mutant cell lines. Half-maximal activation occurred for test depolarizations in the range of -7 to -11 mV. Half-maximal inactivation occurred for pre-pulses in the range of -62 to -69 mV. Scorpion toxin from Leiurus quinquestriatus (100 to 200 nM) increased the time constant for sodium channel inactivation 6- to 9-fold, increased the peak sodium current 2.0 +/- 0.5-fold, shifted the voltage dependence of sodium channel activation 7 to 11 mV to more negative potentials, and made the voltage dependence of inactivation less steep. These effects were observed for both normal and scorpion toxin-resistant neuroblastoma cells. However, the effect of Leiurus toxin on the rate of inactivation was half-maximal at 1.7 nM for the parental cell line N18, in contrast to 5.4 or 39 nM for the scorpion toxin-resistant clone LV30 and 24 or 51 nM for LV10. These results show that scorpion toxin resistance results from a specific change in channel properties that does not impair normal function but causes an increase in the apparent KD for Leiurus toxin action on sodium channels.
采用全细胞膜片钳配置下的千兆欧姆封接记录方法,测量正常和抗蝎毒素神经母细胞瘤细胞中电压敏感性钠通道介导的钠电流。正常细胞系和突变细胞系中钠电流的电压和时间依赖性相似。测试去极化在-7至-11 mV范围内时发生半数最大激活。预脉冲在-62至-69 mV范围内时发生半数最大失活。来自黄蝎(Leiurus quinquestriatus)的蝎毒素(100至200 nM)使钠通道失活的时间常数增加6至9倍,使钠电流峰值增加2.0±0.5倍,使钠通道激活的电压依赖性向更负电位方向移动7至11 mV,并使失活的电压依赖性变缓。在正常和抗蝎毒素神经母细胞瘤细胞中均观察到这些效应。然而,黄蝎毒素对亲本细胞系N18失活速率的影响在1.7 nM时达到半数最大效应,相比之下,抗蝎毒素克隆LV30为5.4或39 nM,LV10为24或51 nM。这些结果表明,抗蝎毒素是由通道特性的特定变化引起的,这种变化不会损害正常功能,但会导致黄蝎毒素对钠通道作用的表观解离常数(KD)增加。