Michael Barber Centre for Mass Spectrometry, Manchester Interdisciplinary Biocentre, School of Chemistry, University of Manchester, Manchester, United Kingdom.
J Am Soc Mass Spectrom. 2009 Dec;20(12):2211-20. doi: 10.1016/j.jasms.2009.08.009. Epub 2009 Aug 27.
Quantification of the stoichiometry of phosphorylation is usually achieved using a mixture of phosphatase treatment and differential isotopic labeling. Here, we introduce a new approach to the concomitant determination of absolute protein concentration and the stoichiometry of phosphorylation at predefined sites. The method exploits QconCAT to quantify levels of phosphorylated and nonphosphorylated peptide sequences in a phosphoprotein. The nonphosphorylated sequence is used to determine the absolute protein quantity and serves as a reference to calculate the extent of phosphorylation at the second peptide. Thus, the stoichiometry of phosphorylation and the absolute protein concentration can be determined accurately in a single experiment.
通常使用磷酸酶处理和差异同位素标记的混合物来定量磷酸化的化学计量。在这里,我们介绍了一种新的方法,可以同时确定预定位点的磷酸化和绝对蛋白质浓度的化学计量。该方法利用 QconCAT 来定量磷酸化和非磷酸化肽序列在磷酸蛋白中的水平。非磷酸化序列用于确定绝对蛋白质量,并作为计算第二个肽段磷酸化程度的参考。因此,在单个实验中可以准确地确定磷酸化的化学计量和绝对蛋白质浓度。