Department of Bioinformatics and Computational Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
J Proteome Res. 2013 Feb 1;12(2):594-604. doi: 10.1021/pr300624g. Epub 2013 Jan 16.
Isobaric tags for relative and absolute quantitation (iTRAQ) is a prominent mass spectrometry technology for protein identification and quantification that is capable of analyzing multiple samples in a single experiment. Frequently, iTRAQ experiments are carried out using an aliquot from a pool of all samples, or "masterpool", in one of the channels as a reference sample standard to estimate protein relative abundances in the biological samples and to combine abundance estimates from multiple experiments. In this manuscript, we show that using a masterpool is counterproductive. We obtain more precise estimates of protein relative abundance by using the available biological data instead of the masterpool and do not need to occupy a channel that could otherwise be used for another biological sample. In addition, we introduce a simple statistical method to associate proteomic data from multiple iTRAQ experiments with a numeric response and show that this approach is more powerful than the conventionally employed masterpool-based approach. We illustrate our methods using data from four replicate iTRAQ experiments on aliquots of the same pool of plasma samples and from a 406-sample project designed to identify plasma proteins that covary with nutrient concentrations in chronically undernourished children from South Asia.
相对和绝对定量的同位素标记技术(iTRAQ)是一种用于蛋白质鉴定和定量的重要质谱技术,能够在单次实验中分析多个样本。通常,iTRAQ 实验使用混合所有样本的等分试样(或“主池”)之一作为参考样品标准,以估计生物样品中蛋白质的相对丰度,并结合来自多个实验的丰度估计值。在本文中,我们表明使用主池是适得其反的。我们通过使用可用的生物学数据而不是主池来获得更精确的蛋白质相对丰度估计值,并且不需要占用原本可以用于另一个生物样本的通道。此外,我们引入了一种简单的统计方法,将来自多个 iTRAQ 实验的蛋白质组学数据与数值响应相关联,并表明这种方法比传统的基于主池的方法更有效。我们使用来自同一血浆样本主池等分试样的四个重复 iTRAQ 实验的数据以及一个 406 样本项目的数据来说明我们的方法,该项目旨在鉴定与南亚长期营养不良儿童营养浓度相关的血浆蛋白质。