Nakamura Tatsuji, Kuromitsu Junro, Oda Yoshiya
Eisai Company Ltd., Laboratory of Core Technology, Ibaraki, Japan.
J Proteome Res. 2008 Mar;7(3):1007-11. doi: 10.1021/pr7005878. Epub 2008 Feb 2.
Two-dimensional liquid-chromatographic (LC) separation followed by mass spectrometric (MS) analysis was examined for the identification of peptides in complex mixtures as an alternative to widely used two-dimensional gel electrophoresis followed by MS analysis for use in proteomics. The present method involves the off-line coupling of a narrow-bore, polymer-based, reversed-phase column using an acetonitrile gradient in an alkaline mobile phase in the first dimension with octadecylsilanized silica (ODS)-based nano-LC/MS in the second dimension. After the first separation, successive fractions were acidified and dried off-line, then loaded on the second dimension column. Both columns separate peptides according to hydrophobicity under different pH conditions, but more peptides were identified than with the conventional technique for shotgun proteomics, that is, the combination of a strong cation exchange column with an ODS column, and the system was robust because no salts were included in the mobile phases. The suitability of the method for proteomics measurements was evaluated.
研究了二维液相色谱(LC)分离后进行质谱(MS)分析,用于鉴定复杂混合物中的肽段,以此作为蛋白质组学中广泛使用的二维凝胶电泳后进行MS分析的替代方法。本方法包括在第一维中使用基于聚合物的窄孔反相柱,在碱性流动相中采用乙腈梯度,与第二维中基于十八烷基硅烷化硅胶(ODS)的纳升LC/MS进行离线联用。第一次分离后,将连续的馏分离线酸化并干燥,然后加载到第二维柱上。两根柱子都在不同pH条件下根据疏水性分离肽段,但与传统的鸟枪法蛋白质组学技术(即强阳离子交换柱与ODS柱的组合)相比,鉴定出的肽段更多,并且该系统很稳定,因为流动相中不含有盐。评估了该方法用于蛋白质组学测量的适用性。