Mager Thomas, Wood Phillip G, Bamberg Ernst
Max Planck Institute of Biophysics, Department of Biophysical Chemistry, 60438 Frankfurt am Main, Germany.
J Mol Biol. 2017 Mar 24;429(6):911-921. doi: 10.1016/j.jmb.2017.02.004. Epub 2017 Feb 10.
Ca concentration jumps for the activation of Ca-dependent ion channels or transporters can be obtained either by fast solution exchange or by the use of caged Ca. Here, we report on an alternate optogenetic method for the activation of Ca and voltage-dependent large conductance (BK) potassium channels. This was achieved through the use of the light-gated channelrhodopsin 2 variant, CatCh(Calcium translocating Channelrhodopsin) with enhanced Ca, which produces locally [Ca] in the μM range on the inner side of the membrane, without significant [Ca] increase in the cytosol. BK channel subunits α and β1 were expressed together with CatCh in HEK293 cells, and voltage and Ca dependence were analyzed. Light activation of endogenous BK channels under native conditions in astrocytes and glioma cells was also investigated. Additionally, BK channels were used as sensors for the calibration of the [Ca] on the inner surface of the cell membrane.
通过快速溶液交换或使用笼形钙可以获得用于激活钙依赖性离子通道或转运蛋白的钙浓度跃升。在此,我们报告一种用于激活钙和电压依赖性大电导(BK)钾通道的替代光遗传学方法。这是通过使用光门控通道视紫红质2变体CatCh(钙转运通道视紫红质)实现的,其具有增强的钙,在膜内侧产生微摩尔范围内的局部[Ca],而胞质溶胶中的[Ca]没有显著增加。BK通道亚基α和β1与CatCh一起在HEK293细胞中表达,并分析了电压和钙依赖性。还研究了在星形胶质细胞和胶质瘤细胞的天然条件下内源性BK通道的光激活。此外,BK通道被用作校准细胞膜内表面[Ca]的传感器。