Department of Biochemistry, Brandeis University, Waltham, MA.
Department of Biochemistry, Brandeis University, Waltham, MA
J Gen Physiol. 2018 Jul 2;150(7):1035-1043. doi: 10.1085/jgp.201812015. Epub 2018 Jun 11.
The mitochondrial calcium uniporter is a multisubunit Ca channel that mediates mitochondrial Ca uptake, a cellular process crucial for the regulation of oxidative phosphorylation, intracellular Ca signaling, and apoptosis. In the last few years, genes encoding uniporter proteins have been identified, but a lack of efficient tools for electrophysiological recordings has hindered quantitative analysis required to determine functional mechanisms of this channel complex. Here, we redirected Ca-conducting subunits (MCU and EMRE) of the human uniporter to the plasma membrane of oocytes. Two-electrode voltage clamp reveals inwardly rectifying Ca currents blocked by a potent inhibitor, Ru360 (half maximal inhibitory concentration, ~4 nM), with a divalent cation conductivity of Ca > Sr > Ba, Mn, and Mg Patch clamp recordings further reveal macroscopic and single-channel Ca currents sensitive to Ru360. These electrical phenomena were abolished by mutations that perturb MCU-EMRE interactions or disrupt a Ca-binding site in the pore. Altogether, this work establishes a robust method that enables deep mechanistic scrutiny of the uniporter using classical strategies in ion channel electrophysiology.
线粒体钙单向转运蛋白是一种多亚基 Ca 通道,介导线粒体 Ca 摄取,这是细胞过程对于氧化磷酸化、细胞内 Ca 信号和细胞凋亡的调节至关重要。在过去的几年中,编码单向转运蛋白蛋白的基因已经被鉴定出来,但缺乏有效的电生理记录工具阻碍了对该通道复合物功能机制的定量分析。在这里,我们将人类单向转运蛋白的 Ca 导肽(MCU 和 EMRE)重新导向卵母细胞的质膜。双电极电压钳揭示了内向整流 Ca 电流被有效抑制剂 Ru360 阻断(半最大抑制浓度,~4 nM),其对二价阳离子的电导率为 Ca> Sr> Ba、Mn 和 Mg。膜片钳记录进一步显示对 Ru360 敏感的宏观和单通道 Ca 电流。这些电现象被破坏 MCU-EMRE 相互作用或破坏孔中 Ca 结合位点的突变所消除。总的来说,这项工作建立了一种稳健的方法,使用离子通道电生理学中的经典策略,能够深入研究单向转运蛋白的机制。