CNC - Center for Neuroscience and Cell Biology, UC-Biotech, University of Coimbra, Cantanhede, Portugal.
Methods Mol Biol. 2021;2310:161-178. doi: 10.1007/978-1-0716-1433-4_10.
Mitochondria play a key role in cell death and its regulation. The permeabilization of the outer mitochondrial membrane, which is mainly controlled by proteins of the BCL-2 family, is a key event that can be directly induced by different signaling pathways, including p53-mediated, and results in the release of proapoptotic factors to the cytosol, such as cytochrome c, second mitochondria-derived activator of caspases/direct inhibitor-of-apoptosis (IAP) binding protein with low pI (SMAC/Diablo), Omi serine protease (Omi/HtrA2), apoptosis-inducing factor (AIF), or endonuclease G (Endo-G). Hence, the determination of subcellular localization of these proteins is extremely important to predict cell fate and elucidate the specific mechanism of apoptosis. Here we describe experimental protocols that can be used to study the subcellular location of different proapoptotic proteins to be used in basic cell biology and toxicology studies.
线粒体在细胞死亡及其调控中发挥着关键作用。线粒体膜通透性的增加主要由 BCL-2 家族的蛋白来控制,这是一个关键事件,可以被不同的信号通路直接诱导,包括 p53 介导的,导致促凋亡因子如细胞色素 c、第二线粒体衍生的半胱天冬酶激活剂/直接凋亡抑制剂(IAP)结合蛋白低 pI(SMAC/Diablo)、Omi 丝氨酸蛋白酶(Omi/HtrA2)、凋亡诱导因子(AIF)或内切核酸酶 G(Endo-G)释放到细胞质中。因此,这些蛋白质的亚细胞定位的确定对于预测细胞命运和阐明凋亡的具体机制非常重要。在这里,我们描述了可用于研究不同促凋亡蛋白的亚细胞定位的实验方案,这些蛋白可用于基础细胞生物学和毒理学研究。