Bioanalytical Mass Spectrometry Group, Max Planck Institute for Biophysical Chemistry, Göttingen, Germany.
Proteomics. 2013 May;13(9):1417-22. doi: 10.1002/pmic.201200366. Epub 2013 Apr 4.
Simple protein separation by 1DE is a widely used method to reduce sample complexity and to prepare proteins for mass spectrometric identification via in-gel digestion. While several automated solutions are available for in-gel digestion particularly of small cylindric gel plugs derived from 2D gels, the processing of larger 1D gel-derived gel bands with liquid handling work stations is less well established in the field. Here, we introduce a digestion device tailored to this purpose and validate its performance in comparison to manual in-gel digestion. For relative quantification purposes, we extend the in-gel digestion procedure by iTRAQ labeling of the tryptic peptides and show that automation of the entire workflow results in robust quantification of proteins from samples of different complexity and dynamic range. We conclude that automation improves accuracy and reproducibility of our iTRAQ workflow as it minimizes the variability in both, digestion and labeling efficiency, the two major causes of irreproducible results in chemical labeling approaches.
一维电泳(1DE)进行简单的蛋白质分离是一种广泛应用的方法,可以降低样品复杂性,并通过胶内消化准备用于质谱鉴定的蛋白质。尽管已经有几种自动化解决方案可用于胶内消化,特别是针对从小型圆柱凝胶块(来自 2D 凝胶)中提取的蛋白质,但是在该领域,使用液体处理工作站处理更大的一维电泳衍生凝胶条带的方法还不太完善。在这里,我们引入了一种专门为此目的设计的消化装置,并将其性能与手动胶内消化进行了比较。为了进行相对定量,我们通过胰蛋白酶肽的 iTRAQ 标记扩展了胶内消化程序,并证明整个工作流程的自动化可从不同复杂性和动态范围的样品中获得稳健的蛋白质定量结果。我们得出结论,自动化可提高 iTRAQ 工作流程的准确性和重现性,因为它可以最大程度地减少消化和标记效率两个方面的变异性,这是化学标记方法中不可重现结果的两个主要原因。