Proteomics Core Facility, Biozentrum, University of Basel, Basel, Switzerland.
Proteomics. 2013 Sep;13(17):2567-78. doi: 10.1002/pmic.201300135. Epub 2013 Jul 30.
There is a great interest in reliable ways to obtain absolute protein abundances at a proteome-wide scale. To this end, label-free LC-MS/MS quantification methods have been proposed where all identified proteins are assigned an estimated abundance. Several variants of this quantification approach have been presented, based on either the number of spectral counts per protein or MS1 peak intensities. Equipped with several datasets representing real biological environments, containing a high number of accurately quantified reference proteins, we evaluate five popular low-cost and easily implemented quantification methods (Absolute Protein Expression, Exponentially Modified Protein Abundance Index, Intensity-Based Absolute Quantification Index, Top3, and MeanInt). Our results demonstrate considerably improved abundance estimates upon implementing accurately quantified reference proteins; that is, using spiked in stable isotope labeled standard peptides or a standard protein mix, to generate a properly calibrated quantification model. We show that only the Top3 method is directly proportional to protein abundance over the full quantification range and is the preferred method in the absence of reference protein measurements. Additionally, we demonstrate that spectral count based quantification methods are associated with higher errors than MS1 peak intensity based methods. Furthermore, we investigate the impact of miscleaved, modified, and shared peptides as well as protein size and the number of employed reference proteins on quantification accuracy.
人们对于在全蛋白质组范围内获得可靠的绝对蛋白质丰度的方法非常感兴趣。为此,已经提出了无标记 LC-MS/MS 定量方法,其中所有鉴定的蛋白质都被赋予了估计的丰度。这种定量方法有几种变体,基于每个蛋白质的谱计数或 MS1 峰强度。我们使用了几个代表真实生物环境的数据集,其中包含大量准确定量的参考蛋白质,评估了五种流行的低成本且易于实施的定量方法(绝对蛋白质表达、指数修饰的蛋白质丰度指数、基于强度的绝对定量指数、Top3 和 MeanInt)。我们的结果表明,在实施准确定量的参考蛋白质后,丰度估计得到了显著改善;也就是说,使用掺入稳定同位素标记标准肽或标准蛋白质混合物来生成适当校准的定量模型。我们表明,仅 Top3 方法在整个定量范围内与蛋白质丰度成正比,并且在没有参考蛋白质测量的情况下是首选方法。此外,我们表明基于谱计数的定量方法与基于 MS1 峰强度的方法相比,错误更高。此外,我们研究了错误切割、修饰和共享肽以及蛋白质大小和使用的参考蛋白质数量对定量准确性的影响。