Schmidt Alexander, Bisle Birgit, Kislinger Thomas
Institute for Molecular Systems Biology, ETH, Zürich, Switzerland.
Methods Mol Biol. 2009;492:21-38. doi: 10.1007/978-1-59745-493-3_2.
Proteomics may be defined as the systematic analysis of proteins expressed in a given organism (Electrophoresis 16:1090-1094, 1995). Important technical innovations in mass spectrometry (MS), protein identification methods, and database annotation, over the past decade, now make it possible to routinely identify thousands of proteins in complex biological samples (Nature 422:198-207, 2003). However, to gain new insights regarding fundamental biological questions, accurate protein quantification is also required. In this chapter, we present methods for the biochemical separation of different cellular compartments, two-dimensional chromatographic separation of the constituent peptide populations, and the recently published Spectral Counting Strategy, a label-free MS-based protein quantification technology (Cell 125:173-186, 2006; Anal Chem 76:4193-4201, 2004; Mol Cell Proteomics 4:1487-1502, 2005; Cell 125:1003-1013, 2006; Methods 40:135-142, 2006; Anal Chem 77:6218-6224, 2005; J Proteome Res 5:2339-2347, 2006). Additionally, highly accurate protein quantification based on isotope dilution, describing the isotope coded protein label (ICPL) -- method shall be explained in detail (Mol Cell Proteomics 5:1543-1558, 2006; Proteomics 5:4-15, 2005).
蛋白质组学可定义为对特定生物体中表达的蛋白质进行系统分析(《电泳》16:1090 - 1094,1995年)。在过去十年中,质谱(MS)、蛋白质鉴定方法和数据库注释方面的重要技术创新,如今已使常规鉴定复杂生物样品中的数千种蛋白质成为可能(《自然》422:198 - 207,2003年)。然而,为了获得关于基本生物学问题的新见解,还需要进行准确的蛋白质定量。在本章中,我们介绍了不同细胞区室的生化分离方法、组成肽群体的二维色谱分离方法,以及最近发表的光谱计数策略——一种基于无标记质谱的蛋白质定量技术(《细胞》125:173 - 186,2006年;《分析化学》76:4193 - 4201,2004年;《分子细胞蛋白质组学》4:1487 - 1502,2005年;《细胞》125:1003 - 1013,2006年;《方法》40:135 - 142,2006年;《分析化学》77:6218 - 6224,2005年;《蛋白质组研究杂志》5:2339 - 2347,2006年)。此外,还将详细解释基于同位素稀释的高精度蛋白质定量方法,即同位素编码蛋白质标签(ICPL)法(《分子细胞蛋白质组学》5:1543 - 1558,2006年;《蛋白质组学》5:4 - 15,2005年)。