Ling Shizhang, Sheng Jian-Zhong, Braun Janice E A, Braun Andrew P
Department of Pharmacology and Therapeutics, Faculty of Medicine, University of Calgary, Alberta, Canada.
J Physiol. 2003 Nov 15;553(Pt 1):65-81. doi: 10.1113/jphysiol.2003.051631. Epub 2003 Aug 29.
Large conductance, calcium-activated potassium channels (BKCa channels) are regulated by several distinct mechanisms, including phosphorylation/dephosphorylation events and protein-protein interactions. In this study, we have examined the interaction between BKCa channels and syntaxin 1A, a soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) that is reported to modulate the activity and/or localization of different classes of ion channels. Using a reciprocal co-immunoprecipitation strategy, we observed that native BKCa channels in rat hippocampus co-associate with syntaxin 1A, but not the closely related homologue syntaxin 3. This BKCa channel-syntaxin 1A interaction could be further demonstrated in a non-neuronal cell line (human embryonic kidney (HEK) 293 cells) following co-expression of rat syntaxin 1A and BKCa channels cloned from either mouse brain or bovine aorta. However, co-expression of these same channels with syntaxin 3 did not lead to a detectable protein-protein interaction. Immunofluorescent co-staining of HEK 293 cells expressing BKCa channels and syntaxin 1A demonstrated overlapping distribution of these two proteins in situ. Functionally, co-expression of BKCa channels with syntaxin 1A, but not syntaxin 3, was observed to enhance channel gating and kinetics at low concentrations (1-4 microM) of free cytosolic calcium, but not at higher concentrations (< or = 10 microM), as judged by macroscopic current recordings in excised membrane patches. Interactions between BKCa channels and neighbouring membrane proteins may thus play important roles in regulating the activity and/or distribution of these channels within specialized cellular compartments.
大电导钙激活钾通道(BKCa通道)受多种不同机制调控,包括磷酸化/去磷酸化事件以及蛋白质-蛋白质相互作用。在本研究中,我们检测了BKCa通道与 syntaxin 1A之间的相互作用,syntaxin 1A是一种可溶性N-乙基马来酰亚胺敏感因子附着蛋白受体(SNARE),据报道它可调节不同类型离子通道的活性和/或定位。采用相互免疫共沉淀策略,我们观察到大鼠海马中的天然BKCa通道与syntaxin 1A共同缔合,但不与密切相关的同源物syntaxin 3缔合。在共表达大鼠syntaxin 1A和从小鼠脑或牛主动脉克隆的BKCa通道后,这种BKCa通道与syntaxin 1A的相互作用在非神经元细胞系(人胚肾(HEK)293细胞)中可进一步得到证实。然而,这些相同通道与syntaxin 3的共表达并未导致可检测到的蛋白质-蛋白质相互作用。对表达BKCa通道和syntaxin 1A的HEK 293细胞进行免疫荧光共染色,结果表明这两种蛋白质在原位呈重叠分布。在功能上,通过对切除膜片的宏观电流记录判断,观察到BKCa通道与syntaxin 1A而非syntaxin 3的共表达在游离胞质钙浓度较低(1 - 4 microM)时可增强通道门控和动力学,但在较高浓度(≤10 microM)时则不然。因此,BKCa通道与相邻膜蛋白之间的相互作用可能在调节这些通道在特定细胞区室内的活性和/或分布中发挥重要作用。