Lohrig Katharina, Wolters Dirk
Department of Analytical Chemistry, Ruhr-University Bochum, Universitaetsstr. 150, 44780 Bochum, Germany.
Methods Mol Biol. 2009;564:143-53. doi: 10.1007/978-1-60761-157-8_8.
Over the past years, large-scale analysis of proteomes gained increased interest to obtain a fast but nevertheless comprehensive overview about cellular protein content. While a complete proteome cannot be covered using current technologies because of its enormous diversity, subfractionation to reduce the complexity has become mandatory. While 2D-PAGE is well established as a high-resolution protein separation technique, it suffers from drawbacks, which can be overcome by using peptide separation methods based on multidimensional liquid chromatography. One of these technologies is multidimensional protein identification technology (MudPIT). It consists of two orthogonal separation systems--strong cation exchange (SCX) and reversed phase (RP)--coupled online in an automated fashion to mass spectrometric detection. This method offers the possibility to analyze high-complex peptide mixtures in a single experiment.
在过去几年中,蛋白质组的大规模分析越来越受到关注,以便快速但全面地了解细胞蛋白质含量。由于蛋白质组的巨大多样性,目前的技术无法涵盖完整的蛋白质组,因此进行亚分级以降低复杂性已成为必要。虽然二维聚丙烯酰胺凝胶电泳(2D-PAGE)作为一种高分辨率蛋白质分离技术已得到广泛应用,但它存在一些缺点,而基于多维液相色谱的肽分离方法可以克服这些缺点。其中一种技术是多维蛋白质鉴定技术(MudPIT)。它由两个正交分离系统——强阳离子交换(SCX)和反相(RP)——以自动化方式在线连接到质谱检测。这种方法使得在单个实验中分析高复杂性肽混合物成为可能。