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采用毛细管区带电泳-串联质谱的深度自上而下蛋白质组学:从大肠杆菌蛋白质组中鉴定出 5700 种蛋白质异构体。

Deep Top-Down Proteomics Using Capillary Zone Electrophoresis-Tandem Mass Spectrometry: Identification of 5700 Proteoforms from the Escherichia coli Proteome.

机构信息

Department of Chemistry , Michigan State University , 578 S Shaw Lane , East Lansing , Michigan 48824 , United States.

Department of BioHealth Informatics , Indiana University-Purdue University Indianapolis , 719 Indiana Avenue , Indianapolis , Indiana 46202 , United States.

出版信息

Anal Chem. 2018 May 1;90(9):5529-5533. doi: 10.1021/acs.analchem.8b00693. Epub 2018 Apr 9.

Abstract

Capillary zone electrophoresis (CZE)-tandem mass spectrometry (MS/MS) has been recognized as a useful tool for top-down proteomics. However, its performance for deep top-down proteomics is still dramatically lower than widely used reversed-phase liquid chromatography (RPLC)-MS/MS. We present an orthogonal multidimensional separation platform that couples size exclusion chromatography (SEC) and RPLC based protein prefractionation to CZE-MS/MS for deep top-down proteomics of Escherichia coli. The platform generated high peak capacity (∼4000) for separation of intact proteins, leading to the identification of 5700 proteoforms from the Escherichia coli proteome. The data represents a 10-fold improvement in the number of proteoform identifications compared with previous CZE-MS/MS studies and represents the largest bacterial top-down proteomics data set reported to date. The performance of the CZE-MS/MS based platform is comparable to the state-of-the-art RPLC-MS/MS based systems in terms of the number of proteoform identifications and the instrument time.

摘要

毛细管区带电泳(CZE)-串联质谱(MS/MS)已被公认为用于自上而下蛋白质组学的有用工具。然而,其用于深度自上而下蛋白质组学的性能仍然远低于广泛使用的反相液相色谱(RPLC)-MS/MS。我们提出了一种正交多维分离平台,该平台将尺寸排阻色谱(SEC)和基于 RPLC 的蛋白质预分级与 CZE-MS/MS 相结合,用于大肠杆菌的深度自上而下蛋白质组学研究。该平台对完整蛋白质的分离产生了高的峰容量(约 4000),从而从大肠杆菌蛋白质组中鉴定出 5700 种蛋白质形式。与之前的 CZE-MS/MS 研究相比,该数据代表了蛋白质形式鉴定数量的 10 倍提高,并且代表了迄今为止报道的最大细菌自上而下蛋白质组学数据集。就蛋白质形式鉴定数量和仪器时间而言,基于 CZE-MS/MS 的平台的性能可与最先进的基于 RPLC-MS/MS 的系统相媲美。

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