Department of Biochemistry and Molecular Biology, University of Southern Denmark, Odense, Denmark.
Proteomics. 2013 Mar;13(6):910-31. doi: 10.1002/pmic.201200484.
Phosphorylation, the reversible addition of a phosphate group to amino acid side chains of proteins, is a fundamental regulator of protein activity, stability, and molecular interactions. Most cellular processes, such as inter- and intracellular signaling, protein synthesis, degradation, and apoptosis, rely on phosphorylation. This PTM is thus involved in many diseases, rendering localization and assessment of extent of phosphorylation of major scientific interest. MS-based phosphoproteomics, which aims at describing all phosphorylation sites in a specific type of cell, tissue, or organism, has become the main technique for discovery and characterization of phosphoproteins in a nonhypothesis driven fashion. In this review, we describe methods for state-of-the-art MS-based analysis of protein phosphorylation as well as the strategies employed in large-scale phosphoproteomic experiments with focus on the various challenges and limitations this field currently faces.
磷酸化是一种将磷酸基团可逆地添加到蛋白质氨基酸侧链上的过程,是蛋白质活性、稳定性和分子相互作用的基本调节方式。大多数细胞过程,如细胞内外信号转导、蛋白质合成、降解和细胞凋亡,都依赖于磷酸化。因此,这种翻译后修饰(PTM)与许多疾病有关,使得磷酸化的定位和程度评估成为主要的科学关注点。基于质谱的磷酸蛋白质组学旨在描述特定类型的细胞、组织或生物体中的所有磷酸化位点,已经成为一种非假设驱动的方式来发现和描述磷酸蛋白质的主要技术。在这篇综述中,我们描述了基于质谱的蛋白质磷酸化分析的最新方法,以及在大规模磷酸蛋白质组学实验中采用的策略,重点介绍了该领域目前面临的各种挑战和局限性。