Thompson C H, Fields D M, Olivetti P R, Fuller M D, Zhang Z R, Kubanek J, McCarty N A
School of Biology, Georgia Institute of Technology, 310 Ferst Drive, Atlanta, Georgia 30332-0230, USA.
J Membr Biol. 2005 Nov;208(1):65-76. doi: 10.1007/s00232-005-0818-8.
ClC chloride channels play essential roles in membrane excitability and maintenance of osmotic balance. Despite the recent crystallization of two bacterial ClC-like proteins, the gating mechanism for these channels remains unclear. In this study we tested scorpion venom for the presence of novel peptide inhibitors of ClC channels, which might be useful tools for dissecting the mechanisms underlying ClC channel gating. Recently, it has been shown that a peptide component of venom from the scorpion L. quinquestriatus hebraeus inhibits the CFTR chloride channel from the intracellular side. Using two-electrode voltage clamp we studied the effect of scorpion venom on ClC-0, -1, and -2, and found both dose- and voltage-dependent inhibition only of ClC-2. Comparison of voltage-dependence of inhibition by venom to that of known pore blockers revealed opposite voltage dependencies, suggesting different mechanisms of inhibition. Kinetic data show that venom induced slower activation kinetics compared to pre-venom records, suggesting that the active component(s) of venom may function as a gating modifier at ClC-2. Trypsinization abolished the inhibitory activity of venom, suggesting that the component(s) of scorpion venom that inhibits ClC-2 is a peptide.
氯离子通道(ClC)在膜兴奋性和渗透压平衡维持中发挥着重要作用。尽管最近两种细菌类ClC蛋白已结晶,但这些通道的门控机制仍不清楚。在本研究中,我们检测了蝎毒中是否存在ClC通道的新型肽抑制剂,这可能是剖析ClC通道门控机制的有用工具。最近有研究表明,以色列金蝎毒液中的一种肽成分可从细胞内侧抑制囊性纤维化跨膜传导调节因子(CFTR)氯离子通道。我们使用双电极电压钳研究了蝎毒对ClC-0、-1和-2的影响,发现仅对ClC-2有剂量和电压依赖性抑制作用。将毒液抑制作用的电压依赖性与已知孔道阻滞剂的进行比较,发现二者电压依赖性相反,提示抑制机制不同。动力学数据表明,与毒液处理前记录相比,毒液诱导的激活动力学更慢,这表明毒液的活性成分可能作为ClC-2的门控修饰剂发挥作用。胰蛋白酶处理消除了毒液的抑制活性,提示蝎毒中抑制ClC-2的成分是一种肽。