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

机译: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

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摘要

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.
机译:解吸电喷雾电离质谱法(DESI-MS)是该领域的最新重要进展,已在固体样品的表面分析中得到广泛应用,但也已扩展到液体样品的分析中。液体样品DESI通常使用一块熔融石英毛细管来转移液体样品进行电离。在这项研究中,我们通过用填充有色谱固定相材料(例如C4,C18)的捕集柱代替样品传输硅胶毛细管来介绍液体样品DESI-MS的改进。这种类型的捕集柱/液体样品DESI可用于痕量分析有机物和生物分子,例如高盐含量基质中的蛋白质/肽(nM浓度)。此外,当样品传输毛细管被共价键合在其毛细管内壁上的酶修饰时,可以实现蛋白质(如磷蛋白)的快速消化(<6分钟),并且可以使用DESI以高灵敏度直接电离在线消化的蛋白质。后者归因于为DESI分析选择合适的喷雾溶剂的自由。我们的数据表明,带有改进的样品传输毛细管的液体样品DESI-MS已大大扩展了其在生物分析中的效用。

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