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Simultaneous Measurement of Individual Mitochondrial Membrane Potential and Electrophoretic Mobility by Capillary Electrophoresis

机译:毛细管电泳同时测量单个线粒体膜电位和电泳迁移率

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Mitochondrial membrane potential varies, depending on energy demand, subcellular location, and morphology and is commonly used as an indicator of mitochondrial functional status. Electrophoretic mobility is a heterogeneous surface property reflective of mitochondrial surface composition and morphology, which could be used as a basis for separation of mitochondrial subpopulations. Since these properties are heterogeneous, methods for their characterization in individual mitochondria are needed to better design and understand electrophoretic separations of subpopulations of mitochondria. Here we report on the first method for simultaneous determination of individual mitochondrial membrane potential and electrophoretic mobility by capillary electrophoresis with laser-induced fluorescence detection (CE-LIF). Mitochondria were isolated from cultured cells, mouse muscle, or liver, and then polarized, labeled with JC-1 (a ratiometric fluorescent probe, which indicates changes in membrane potential), and separated with CE-LIF. Red/green fluorescence intensity ratios from individual mitochondria were used as an indicator of mitochondrial membrane potential. Reproducible distributions of individual mitochondrial membrane potential and electrophoretic mobility were observed. Analysis of polarized and depolarized regions of interest defined using red/green ratios and runs of depolarized controls allowed for the determination of membrane potential and comparison of electrophoretic mobility distributions in preparations containing depolarized mitochondria. Through comparison of these regions of interest, we observed dependence of electrophoretic mobility on membrane potential, with polarized regions of interest displaying decreased electrophoretic mobility. This method could be applied to investigate mitochondrial heterogeneity in aging or disease models where membrane potential is an important factor.
机译:线粒体膜电位根据能量需求,亚细胞位置和形态而变化,通常用作线粒体功能状态的指标。电泳迁移率是反映线粒体表面组成和形态的异质表面性质,可作为分离线粒体亚群的基础。由于这些特性是异质的,因此需要在单个线粒体中表征它们的方法,以更好地设计和了解线粒体亚群的电泳分离。在这里,我们报告的第一种方法通过毛细管电泳与激光诱导的荧光检测(CE-LIF)同时测定单个线粒体膜电位和电泳迁移率。从培养的细胞,小鼠肌肉或肝脏中分离出线粒体,然后极化,用JC-1(比例荧光探针,指示膜电位的变化)标记,并用CE-LIF分离。来自单个线粒体的红色/绿色荧光强度比用作线粒体膜电位的指标。观察到单个线粒体膜电位和电泳迁移率的可复制分布。使用红色/绿色比率定义的极化和去极化感兴趣区域的分析以及去极化对照的运行,可以确定膜电位并比较包含去极化线粒体的制剂中的电泳迁移率分布。通过比较这些感兴趣的区域,我们观察到电泳迁移率对膜电位的依赖性,其中极化的感兴趣区域显示出降低的电泳迁移率。该方法可用于研究膜电位是重要因素的衰老或疾病模型中的线粒体异质性。

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