Scholz-Starke Joachim, Carpaneto Armando, Gambale Franco
Istituto di Biofisica, Consiglio Nazionale delle Ricerche, 16149 Genoa, Italy.
J Gen Physiol. 2006 Mar;127(3):329-40. doi: 10.1085/jgp.200509402.
This study investigates the interaction of the aminoglycoside antibiotic neomycin with the slow vacuolar (SV) channel in vacuoles from Arabidopsis thaliana mesophyll cells. Patch-clamp experiments in the excised patch configuration revealed a complex pattern of neomycin effects on the channel: applied at concentrations in the submicromolar to millimolar range neomycin (a) blocked macroscopic SV currents in a voltage- and concentration-dependent manner, (b) slowed down activation and deactivation kinetics of the channel, and most interestingly, (c) at concentrations above 10 muM, neomycin shifted the SV activation threshold towards negative membrane potentials, causing a two-phasic activation at high concentrations. Single channel experiments showed that neomycin causes these macroscopic effects by combining a decrease of the single channel conductance with a concomitant increase of the channel's open probability. Our results clearly demonstrate that the SV channel can be activated at physiologically relevant tonoplast potentials in the presence of an organic effector molecule. We therefore propose the existence of a cellular equivalent regulating the activity of the SV channel in vivo.
本研究调查了氨基糖苷类抗生素新霉素与拟南芥叶肉细胞液泡中慢液泡(SV)通道的相互作用。在切除膜片配置下进行的膜片钳实验揭示了新霉素对该通道影响的复杂模式:在亚微摩尔至毫摩尔范围内的浓度下施加新霉素,(a)以电压和浓度依赖性方式阻断宏观SV电流,(b)减慢通道的激活和失活动力学,最有趣的是,(c)在浓度高于10μM时,新霉素将SV激活阈值向负膜电位移动,在高浓度下导致双相激活。单通道实验表明,新霉素通过结合单通道电导的降低和通道开放概率的同时增加而产生这些宏观效应。我们的结果清楚地表明,在存在有机效应分子的情况下,SV通道可以在生理相关的液泡膜电位下被激活。因此,我们提出存在一种在体内调节SV通道活性的细胞等效物。