Institute for Systems Biology, Seattle, Washington 98103, USA.
J Am Soc Mass Spectrom. 2010 Aug;21(8):1417-22. doi: 10.1016/j.jasms.2010.04.002. Epub 2010 Apr 8.
Stable incorporation of labeled amino acids in cell culture is a simple approach to label proteins in vivo for mass spectrometric quantification. Full incorporation of isotopically heavy amino acids facilitates accurate quantification of proteins from different cultures, yet analysis methods for determination of incorporation are cumbersome and time-consuming. We present QTIPS, Quantification by Total Identified Peptides for SILAC, a straightforward, accurate method to determine the level of heavy amino acid incorporation throughout a population of peptides detected by mass spectrometry. Using QTIPS, we show that the incorporation of heavy amino acids in baker's yeast is unaffected by the use of prototrophic strains, indicating that auxotrophy is not a requirement for SILAC experiments in this organism. This method has general utility for multiple applications where isotopic labeling is used for quantification in mass spectrometry.
细胞培养中稳定掺入标记氨基酸是一种将蛋白质在体内进行标记用于质谱定量的简单方法。完全掺入同位素标记的重氨基酸有助于从不同培养物中准确定量蛋白质,但用于确定掺入的分析方法繁琐且耗时。我们提出了 QTIPS(稳定同位素标记相对和绝对定量的总鉴定肽),这是一种通过质谱检测到的肽的总数鉴定肽来定量 SILAC 的简单、准确的方法。使用 QTIPS,我们表明,在面包酵母中,重氨基酸的掺入不受使用营养缺陷型菌株的影响,这表明在该生物中,营养缺陷型不是 SILAC 实验的必要条件。该方法在需要使用同位素标记进行质谱定量的多种应用中具有普遍适用性。