Department of Chemistry, Michigan State University, East Lansing, Michigan, USA 48824.
Analyst. 2017 Jun 21;142(12):2118-2127. doi: 10.1039/c7an00509a. Epub 2017 May 17.
Better peptide separation is required for bottom-up proteomics for further improving the proteome coverage. The two-dimensional liquid chromatography (2D-LC) systems only explore differences among peptides in their hydrophobicity (reversed-phase, RP) and charge (strong cation/anion exchange, SCX/SAX). Alternative separation techniques with different separation mechanisms are required to further improve the separation. Capillary zone electrophoresis (CZE) is an attractive alternative because it has high efficiency for separation of biomolecules and it separates analytes based on their size-to-charge ratios, complementary with LC. However, the low loading capacity and narrow separation window of CZE limit its wide application for large-scale proteomics. In this manuscript, we present an automated CZE-mass spectrometry (MS) system for solving those issues. The CZE-MS system can approach at least half-a-microliter loading capacity with good robustness and reproducibility, can routinely use over 12% of the available sample in the sample vial for analysis, and can generate a 140 min separation window and high peak capacity (∼380) for complex proteome analysis. The results represent the highest peak capacity and the widest separation window of CZE for peptide separation with a microliter-scale loading capacity. It is the first time that CZE-MS approaches both the microliter-scale loading capacity and over 2-hour separation window for analysis of complex samples. The automated CZE-MS system dramatically reduces the gap between CZE-MS and RPLC-MS in terms of loading capacity, separation window and peak capacity. It truly opens the door for large-scale bottom-up proteomics using CZE-MS.
为了进一步提高蛋白质组覆盖度,需要更好的肽段分离效果,用于自上而下的蛋白质组学研究。二维液相色谱(2D-LC)系统仅能探索肽段疏水性(反相,RP)和电荷(强阳离子/阴离子交换,SCX/SAX)的差异。需要使用具有不同分离机制的替代分离技术,以进一步改善分离效果。毛细管区带电泳(CZE)是一种很有吸引力的替代方法,因为它对生物分子的分离具有高效率,并且基于其大小-电荷比来分离分析物,与 LC 互补。然而,CZE 的低上样量和窄分离窗口限制了其在大规模蛋白质组学中的广泛应用。在本手稿中,我们提出了一种自动化的 CZE-质谱(MS)系统来解决这些问题。该 CZE-MS 系统可以实现至少半微升的上样量,具有良好的稳健性和重现性,常规情况下可以从样品管中使用超过 12%的可用样品进行分析,并且可以生成 140 分钟的分离窗口和高峰容量(约 380),用于复杂蛋白质组分析。结果代表了 CZE 用于微升上样量的肽段分离的最高峰容量和最宽的分离窗口。这是首次使用 CZE-MS 达到微升上样量和超过 2 小时的分离窗口,用于分析复杂样品。自动化 CZE-MS 系统在进样量、分离窗口和峰容量方面极大地缩小了 CZE-MS 和 RPLC-MS 之间的差距。它真正为使用 CZE-MS 进行大规模的自上而下的蛋白质组学研究打开了大门。