Alonso María Teresa, Navas-Navarro Paloma, García-Sancho Javier
Instituto de Biología y Genética Molecular (IBGM), Universidad de Valladolid y Consejo Superior de Investigaciones Científicas (CSIC), c/ Sanz y Forés 3, 47003, Valladolid, Spain.
Methods Mol Biol. 2017;1567:245-253. doi: 10.1007/978-1-4939-6824-4_15.
Mitochondrial Ca homeostasis is crucial for regulating vital functions such as respiration or apoptosis. Targeted aequorins are excellent probes to measure subcellular Ca. Ca concentration in mitochondria ([Ca]) is low at rest (about 10 M) and can increase to the micromolar or even approach the millimolar range, upon cell activation. Here we describe a new quantitative luminescent protocol to directly measure mitochondrial Ca uptake, optimized for high throughput. The sensitivity of the method allows detection of changes in either the capacity or the affinity of mitochondrial Ca transport.
线粒体钙稳态对于调节呼吸或细胞凋亡等重要功能至关重要。靶向水母发光蛋白是测量亚细胞钙的优秀探针。线粒体中的钙浓度([Ca])在静息时较低(约10⁻⁷M),在细胞激活后可增加到微摩尔甚至接近毫摩尔范围。在此,我们描述了一种新的定量发光方案,用于直接测量线粒体钙摄取,该方案针对高通量进行了优化。该方法的灵敏度能够检测线粒体钙转运能力或亲和力的变化。