Biotechnology and Bioengineering Center, Medical College of Wisconsin, WI, USA.
Proteomics. 2010 Apr;10(7):1408-15. doi: 10.1002/pmic.200900684.
We report a new quantitative proteomics approach that combines the best aspects of stable isotope labeling of amino acids in cell culture (SILAC) labeling and spectral counting. The SILAC peptide count ratio analysis (SPeCtRA, http://proteomics.mcw.edu/visualize) method relies on MS(2) spectra rather than ion chromatograms for quantitation and therefore does not require the use of high mass accuracy mass spectrometers. The inclusion of a stable isotope label allows the samples to be combined before sample preparation and analysis, thus avoiding many of the sources of variability that can plague spectral counting. To validate the SPeCtRA method, we have analyzed samples constructed with known ratios of protein abundance. Finally, we used SPeCtRA to compare endothelial cell protein abundances between high (20 mM) and low (11 mM) glucose culture conditions. Our results demonstrate that SPeCtRA is a protein quantification technique that is accurate and sensitive as well as easy to automate and apply to high-throughput analysis of complex biological samples.
我们报告了一种新的定量蛋白质组学方法,它结合了稳定同位素标记的氨基酸在细胞培养中的最佳方面(SILAC)标记和光谱计数。SILAC 肽计数比分析(SPeCtRA,http://proteomics.mcw.edu/visualize)方法依赖于 MS(2)光谱而不是离子色谱图进行定量,因此不需要使用高质量精度的质谱仪。包含稳定同位素标记允许在样品制备和分析之前将样品组合,从而避免了许多可能困扰光谱计数的可变性来源。为了验证 SPeCtRA 方法,我们已经分析了用已知蛋白丰度比构建的样品。最后,我们使用 SPeCtRA 比较了高(20 mM)和低(11 mM)葡萄糖培养条件下内皮细胞蛋白丰度。我们的结果表明,SPeCtRA 是一种准确、敏感、易于自动化且适用于复杂生物样品高通量分析的蛋白质定量技术。