Sylvestersen Kathrine B, Nielsen Michael L
Department of Proteomics, The Novo Nordisk Foundation Center for Protein Research, University of Copenhagen, Faculty of Health Sciences, Copenhagen, Denmark.
Curr Protoc Protein Sci. 2015 Nov 2;82:24.7.1-24.7.17. doi: 10.1002/0471140864.ps2407s82.
The attachment of one or more methylation groups to the side chain of arginine residues is a regulatory mechanism for cellular proteins. Recent advances in mass spectrometry-based characterization allow comprehensive identification of arginine methylation sites by peptide-level enrichment strategies. Described in this unit is a 4-day protocol for enrichment of arginine-methylated peptides and subsequent identification of thousands of distinct sites by mass spectrometry. Specifically, the protocol explains step-by-step sample preparation, enrichment using commercially available antibodies, prefractionation using strong cation exchange, and identification using liquid chromatography coupled to tandem mass spectrometry. A strategy for relative quantification is described using stable isotope labeling by amino acids in cell culture (SILAC). Approaches for analysis of arginine methylation site occupancy are also discussed. Collectively, the unit describes the essential parameters required for a successful and comprehensive experiment detailing the arginine methylome.
一个或多个甲基化基团附着于精氨酸残基侧链是细胞蛋白质的一种调节机制。基于质谱的表征技术的最新进展使得通过肽段水平的富集策略能够全面鉴定精氨酸甲基化位点。本单元介绍了一个为期4天的方案,用于富集精氨酸甲基化肽段,并随后通过质谱鉴定数千个不同的位点。具体而言,该方案详细说明了样品制备的步骤、使用市售抗体进行富集、使用强阳离子交换进行预分级分离以及使用液相色谱-串联质谱进行鉴定。还介绍了一种使用细胞培养中氨基酸稳定同位素标记(SILAC)进行相对定量的策略。同时也讨论了分析精氨酸甲基化位点占有率的方法。总体而言,本单元描述了成功全面地进行精氨酸甲基化组实验所需的基本参数。