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使用捕集阱和毛细管柱提高液体样品解吸电喷雾电离质谱的性能

Enhancing Performance of Liquid Sample Desorption Electrospray Ionization Mass Spectrometry Using Trap and Capillary Columns.

作者信息

Cheng Si, Wang Jun, Cai Yi, Loo Joseph A, Chen Hao

机构信息

Center for Intelligent Chemical Instrumentation, Department of Chemistry and Biochemistry, Edison Biotechnology Institute, Ohio University, Athens, OH, 45701, USA.

Center for Intelligent Chemical Instrumentation, Department of Chemistry and Biochemistry, Edison Biotechnology Institute, Ohio University, Athens, OH, 45701, USA ; Department of forensic science, Jiangsu Police Institute, Nanjing, Jiang Su, 210031, China.

出版信息

Int J Mass Spectrom. 2015 Dec 3;392:73-79. doi: 10.1016/j.ijms.2015.09.010.

Abstract

Desorption electrospray ionization mass spectrometry (DESI-MS) is a recent and important advance in the field that has extensive applications in surface analysis of solid samples but has also been extended to analysis of liquid samples. The liquid sample DESI typically employs a piece of fused silica capillary to transfer liquid sample for ionization. In this study, we present the improvement of liquid sample DESI-MS by replacing the sample transfer silica capillary with a trap column filled with chromatographic stationary phase materials (e.g., C4, C18). This type of trap column/liquid sample DESI can be used for trace analysis of organics and biomolecules such as proteins/peptides (in nM concentration) in high salt content matrices. Furthermore, when the sample transfer capillary is modified with enzyme covalently bound on its inside capillary wall, fast digestion (< 6 min) of proteins such as phosphoproteins can be achieved and the online digested proteins can be directly ionized using DESI with high sensitivity. The latter is ascribed to the freedom to select favorable spray solvent for the DESI analysis. Our data shows that liquid sample DESI-MS with a modified sample transfer capillary has significantly expanded its utility in bioanalysis.

摘要

解吸电喷雾电离质谱法(DESI-MS)是该领域一项最新且重要的进展,它在固体样品的表面分析中有广泛应用,但也已扩展到液体样品的分析。液体样品DESI通常采用一根熔融石英毛细管来转移液体样品以进行电离。在本研究中,我们通过用填充有色谱固定相材料(例如C4、C18)的捕集柱替换样品转移硅胶毛细管,对液体样品DESI-MS进行了改进。这种捕集柱/液体样品DESI可用于高盐含量基质中有机物和生物分子(如蛋白质/肽,浓度为纳摩尔级)的痕量分析。此外,当样品转移毛细管在其内壁上共价结合酶进行修饰时,可实现磷酸化蛋白等蛋白质的快速消化(<6分钟),并且在线消化后的蛋白质可以使用DESI以高灵敏度直接电离。后者归因于在DESI分析中可以自由选择有利的喷雾溶剂。我们的数据表明,具有改进的样品转移毛细管的液体样品DESI-MS在生物分析中的实用性得到了显著扩展。

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