Institute of Hygiene and Occupational Medicine, University Hospital Essen, Germany.
J Proteomics. 2011 Dec 21;75(2):375-83. doi: 10.1016/j.jprot.2011.08.001. Epub 2011 Aug 10.
Posttranslational modification (PTM) of proteins, particularly phosphorylation, is a key element in the regulation of cell functions. In many signal transduction processes, PTM is a pivotal step. Various analytical methods have been proposed for the identification of phosphoproteins; however, most of these methods require sophisticated equipment. Here we present an easily applicable method of phosphoprotein enrichment. This method is based on single-step precipitation by lanthanum chloride and allows subsequent protein identification by matrix-assisted laser desorption/ionization-mass spectrometry (MALDI-TOF-MS). The method proved its suitability for the isolation of phosphoproteins from frozen tissue and cultured cells samples after cell lysis in various buffer systems (urea/thiourea and EGTA/EDTA). The tests revealed that the isolation of phosphoproteins can be achieved with high efficiency even from complex protein mixtures. Our results indicate that lanthanum-based enrichment of phosphoproteins can be a useful tool in phosphoproteomic studies.
蛋白质的翻译后修饰(PTM),特别是磷酸化,是调节细胞功能的关键因素。在许多信号转导过程中,PTM 是一个关键步骤。已经提出了各种分析方法来鉴定磷酸化蛋白;然而,这些方法大多需要复杂的设备。在这里,我们提出了一种易于应用的磷酸化蛋白富集方法。该方法基于氯化镧的单步沉淀,允许随后通过基质辅助激光解吸/电离 - 飞行时间质谱(MALDI-TOF-MS)进行蛋白质鉴定。该方法已被证明适用于在各种缓冲液系统(尿素/硫脲和 EGTA/EDTA)中裂解细胞后从冷冻组织和培养细胞样品中分离磷酸化蛋白。测试表明,即使从复杂的蛋白质混合物中,也可以高效地分离磷酸化蛋白。我们的结果表明,基于镧的磷酸化蛋白富集可以成为磷酸蛋白质组学研究的有用工具。