Lou Xianwen, van Dongen Joost L J, Milroy Lech-Gustav, Meijer E W
Laboratory of Macromolecular and Organic Chemistry, Eindhoven University of Technology, P.O. Box 513, 5600, MB, Eindhoven, The Netherlands.
Laboratory of Chemical Biology, Department of Biomedical Engineering, Eindhoven University of Technology, P.O. Box 513, 5600, MB, Eindhoven, The Netherlands.
Rapid Commun Mass Spectrom. 2016 Dec 30;30(24):2628-2634. doi: 10.1002/rcm.7741.
Ionization in matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) is a very complicated process. It has been reported that quaternary ammonium salts show extremely strong matrix and analyte suppression effects which cannot satisfactorily be explained by charge transfer reactions. Further investigation of the reasons causing these effects can be useful to improve our understanding of the MALDI process.
The dried-droplet and modified thin-layer methods were used as sample preparation methods. In the dried-droplet method, analytes were co-crystallized with matrix, whereas in the modified thin-layer method analytes were deposited on the surface of matrix crystals. Model compounds, tetrabutylammonium iodide ([N(Bu) ]I), cesium iodide (CsI), trihexylamine (THA) and polyethylene glycol 600 (PEG 600), were selected as the test analytes given their ability to generate exclusively pre-formed ions, protonated ions and metal ion adducts respectively in MALDI.
The strong matrix suppression effect (MSE) observed using the dried-droplet method might disappear using the modified thin-layer method, which suggests that the incorporation of analytes in matrix crystals contributes to the MSE. By depositing analytes on the matrix surface instead of incorporating in the matrix crystals, the competition for evaporation/ionization from charged matrix/analyte clusters could be weakened resulting in reduced MSE. Further supporting evidence for this inference was found by studying the analyte suppression effect using the same two sample deposition methods.
By comparing differences between the mass spectra obtained via the two sample preparation methods, we present evidence suggesting that the generation of gas-phase ions from charged matrix/analyte clusters may induce significant suppression of matrix and analyte ions. The results suggest that the generation of gas-phase ions from charged matrix/analyte clusters is an important ionization step in MALDI-MS. Copyright © 2016 John Wiley & Sons, Ltd.
基质辅助激光解吸/电离质谱(MALDI-MS)中的电离是一个非常复杂的过程。据报道,季铵盐显示出极强的基质和分析物抑制效应,而电荷转移反应无法令人满意地解释这些效应。进一步研究导致这些效应的原因有助于增进我们对MALDI过程的理解。
采用干滴法和改进的薄层法作为样品制备方法。在干滴法中,分析物与基质共结晶,而在改进的薄层法中,分析物沉积在基质晶体表面。选择模型化合物碘化四丁铵([N(Bu)₄]I)、碘化铯(CsI)、三己胺(THA)和聚乙二醇600(PEG 600)作为测试分析物,因为它们在MALDI中分别能够仅产生预形成离子、质子化离子和金属离子加合物。
使用干滴法观察到的强基质抑制效应(MSE)在使用改进的薄层法时可能消失,这表明分析物掺入基质晶体中会导致MSE。通过将分析物沉积在基质表面而不是掺入基质晶体中,可以减弱带电基质/分析物簇蒸发/电离的竞争,从而降低MSE。通过使用相同的两种样品沉积方法研究分析物抑制效应,发现了进一步支持这一推断的证据。
通过比较两种样品制备方法获得的质谱之间的差异,我们提供的证据表明,带电基质/分析物簇产生气相离子可能会显著抑制基质和分析物离子。结果表明,带电基质/分析物簇产生气相离子是MALDI-MS中一个重要的电离步骤。版权所有© 2016约翰威立父子有限公司。