Department of Medical Protein Research, VIB , B-9000 Ghent, Belgium.
J Proteome Res. 2011 Jul 1;10(7):3183-9. doi: 10.1021/pr200219x. Epub 2011 May 23.
Mass spectrometry-driven proteomics is increasingly relying on quantitative analyses for biological discoveries. As a result, different methods and algorithms have been developed to perform relative or absolute quantification based on mass spectrometry data. One of the most popular quantification methods are the so-called label-free approaches, which require no special sample processing, and can even be applied retroactively to existing data sets. Of these label-free methods, the MS/MS-based approaches are most often applied, mainly because of their inherent simplicity as compared to MS-based methods. The main application of these approaches is the determination of relative protein amounts between different samples, expressed as protein ratios. However, as we demonstrate here, there are some issues with the reproducibility across replicates of these protein ratio sets obtained from the various MS/MS-based label-free methods, indicating that the existing methods are not optimally robust. We therefore present two new methods (called RIBAR and xRIBAR) that use the available MS/MS data more effectively, achieving increased robustness. Both the accuracy and the precision of our novel methods are analyzed and compared to the existing methods to illustrate the increased robustness of our new methods over existing ones.
基于质谱的蛋白质组学越来越依赖于定量分析来进行生物学发现。因此,已经开发了不同的方法和算法来根据质谱数据进行相对或绝对定量。最受欢迎的定量方法之一是所谓的无标记方法,它不需要特殊的样品处理,甚至可以 retroactive 应用于现有的数据集。在这些无标记方法中,基于 MS/MS 的方法最常被应用,主要是因为与基于 MS 的方法相比,它们具有固有的简单性。这些方法的主要应用是在不同样品之间测定相对蛋白质含量,以蛋白质比的形式表示。然而,正如我们在这里所展示的,从各种基于 MS/MS 的无标记方法获得的这些蛋白质比率集在重复之间的重现性存在一些问题,这表明现有的方法不是最优的稳健。因此,我们提出了两种新的方法(称为 RIBAR 和 xRIBAR),它们更有效地利用了可用的 MS/MS 数据,从而提高了稳健性。我们对新方法的准确性和精密度进行了分析,并与现有的方法进行了比较,以说明我们的新方法相对于现有的方法具有更高的稳健性。