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Integrated Platform for Proteome Analysis with Combination of Protein and Peptide Separation via Online Digestion

机译:通过在线消化结合蛋白质和多肽分离的蛋白质组分析综合平台

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An integrated platform with the combination of protein and peptide separation was established via online protein digestion, by which proteins were first separated by a microcolumn packed with mixed weak anion and weak cation exchange (WAX/WCX) particles under a series of salt steps, online digested by a trypsin immobilized microenzymatic reactor (IMER), trapped and desalted by two parallel C8 precolumns, separated by microreversed-phase liquid chromatography ((mu)RPLC) under a linear gradient of organic modifier concentration, and finally identified by electrospray ionization-MS/MS (ESI-MS/MS). To evaluate the performance of such a platform, a mixture of myoglobin, cytochrome c, bovine serum albumin (BSA), and alpha-casein, with mass ranging from 25 ng to 2 (mu)g, was analyzed. Compared to the methods by offline protein fractionation and shotgun based strategy, the analysis time, including sample preparation, digestion, desalting, separation, and detection, was shortened from ca. 30 to 5 h, and cytochrome c with abundance of 25 ng could be identified with improved sequence coverage. Furthermore, such an integrated platform was successfully applied into the analysis of proteins extracted from human lung cancer cells. Compared with the results obtained by the shotgun approach, the identified protein number was increased by 30percent. All these results demonstrated that such an integrated approach would be an attractive alternative to commonly applied approaches for proteome research.
机译:通过在线蛋白质消化建立了一个结合蛋白质和多肽分离功能的集成平台,通过该平台,蛋白质首先通过一个微柱分离,该微柱中装有混合的弱阴离子和弱阳离子交换(WAX / WCX)颗粒,经过一系列盐分步骤在线进行用胰蛋白酶固定化微酶反应器(IMER)消化,用两个平行的C8预柱捕集和脱盐,在有机改性剂浓度的线性梯度下,通过微反相液相色谱(μRPLC)分离,最后通过电喷雾电离-MS鉴定/ MS(ESI-MS / MS)。为了评估这种平台的性能,分析了质量范围为25 ng至2μg的肌红蛋白,细胞色素c,牛血清白蛋白(BSA)和α-酪蛋白的混合物。与通过离线蛋白质分级分离和基于散弹枪的策略所采用的方法相比,分析时间(包括样品前处理,消解,脱盐,分离和检测)从原来的大约3天缩短了。 30至5 h,可以鉴定出具有25 ng丰度的细胞色素c,并改善了序列覆盖率。此外,这种集成平台已成功应用于从人肺癌细胞中提取的蛋白质的分析。与通过the弹枪法获得的结果相比,鉴定出的蛋白质数量增加了30%。所有这些结果表明,这种集成方法将是蛋白质组学研究常用方法的有吸引力的替代方法。

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