Renvoisé Margaux, Bonhomme Ludovic, Davanture Marlène, Zivy Michel, Lemaire Claire
UMR 9198 CNRS, Institute for Integrative Biology of the Cell (I2BC), B3S, LPSM-CEA Saclay, 91191, Gif-sur-Yvette cedex, France.
INRA/UCA UMR 1095 GDEC 'Génétique, Diversité et Ecophysiologie des Céréales', 63039, Clermont-Ferrand, France.
Methods Mol Biol. 2017;1636:283-299. doi: 10.1007/978-1-4939-7154-1_18.
Mitochondria play a central role in cellular energy metabolism and cell death. Deregulation of mitochondrial functions is associated with several human pathologies (neurodegenerative diseases, neuromuscular diseases, type II diabetes, obesity, cancer). The steadily increasing number of identified mitochondrial phosphoproteins, kinases, and phosphatases in recent years suggests that reversible protein phosphorylation plays an important part in the control of mitochondrial processes. In addition, many mitochondrial phosphoproteins probably still remain to be identified, considering that 30% of proteins are expected to be phosphorylated in eukaryotes. In this chapter, we describe two procedures for the analysis of the mitochondrial phosphoproteome. The first one is a qualitative method that combines blue native and sodium dodecyl sulfate-polyacrylamide gel electrophoresis (2D-BN/SDS-PAGE) and specific phosphoprotein staining. The second one is a quantitative approach that associates mitochondrial peptide labeling, phosphopeptide enrichment, and mass spectrometry.
线粒体在细胞能量代谢和细胞死亡中起着核心作用。线粒体功能失调与多种人类疾病(神经退行性疾病、神经肌肉疾病、II型糖尿病、肥胖症、癌症)相关。近年来,已鉴定出的线粒体磷酸化蛋白、激酶和磷酸酶的数量不断增加,这表明可逆蛋白磷酸化在控制线粒体过程中起着重要作用。此外,考虑到真核生物中预计有30%的蛋白质会被磷酸化,许多线粒体磷酸化蛋白可能仍有待鉴定。在本章中,我们描述了两种分析线粒体磷酸化蛋白质组的方法。第一种是定性方法,它结合了蓝色天然聚丙烯酰胺凝胶电泳和十二烷基硫酸钠聚丙烯酰胺凝胶电泳(二维蓝色天然/十二烷基硫酸钠聚丙烯酰胺凝胶电泳)以及特异性磷酸化蛋白染色。第二种是定量方法,它将线粒体肽标记、磷酸肽富集和质谱分析相结合。