Selective Gas-Phase Depletion of Chemical Contaminants in Dissolved Organic Matter Increases Compositional Coverage by FT-ICR Mass Spectrometry

IF 3.1 2区 化学 Q2 BIOCHEMICAL RESEARCH METHODS
Chad R. Weisbrod*, Amy M. McKenna and Christopher L. Hendrickson, 
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Abstract

Fourier transform ion cyclotron resonance mass spectrometry of dissolved organic matter (DOM) extracted from environmental samples provides molecular speciation that enables visualization of compositional trends in the fate and cycling of biogenic and anthropogenic organics. Often, chemical contamination is introduced during field sampling (i.e., remote locations, cannot use glass). Further, preconcentration of DOM by solid-phase extraction often results in chemical contamination. When chemical noise is a dominant fraction of the ion signal, mass spectral performance is degraded by reduction of the ion trap analyte accumulation capacity and enhanced ion cloud dephasing during ICR detection. We have developed gas-phase ion depletion of unwanted chemical contaminants during ion injection into the linear RF ion trap of the hybrid linear ion trap 21 T FT-ICR mass spectrometer that improves detection of analytes by removing unwanted chemical noise. We demonstrate improvements in signal-to-noise ratio, dynamic range, and the number of observed analytes in dissolved organic matter samples that results in a 40–100% increase in the number of identified analytes. In many cases, the number of peaks observed per nominal mass more than doubles over select m/z regions. This gas-phase “clean-up” can salvage precious samples challenged by sampling location, sample volume, or collection protocols that cannot be avoided and maximizes the compositional information obtained. Further, this approach is generalizable and extendable to any hybrid linear ion trap instrument platform (e.g., LTQ-Orbitrap or linear ion trap-TOF). We highlight the power of gas-phase depletion with electrospray ionization, but this method is also applicable to other ionization modes.

Abstract Image

溶解有机物中化学污染物的选择性气相损耗提高了傅立叶变换-离子色谱质谱法的成分覆盖率
对从环境样本中提取的溶解有机物(DOM)进行傅立叶变换离子回旋共振质谱分析可提供分子标样,使生物有机物和人为有机物的归宿和循环中的成分趋势可视化。在野外采样过程中,往往会引入化学污染(例如,地点偏远,无法使用玻璃)。此外,通过固相萃取对 DOM 进行预富集往往会造成化学污染。当化学噪声成为离子信号的主要部分时,离子阱的分析物积累能力会降低,ICR 检测过程中的离子云去相现象也会增强,从而降低质谱性能。我们开发了在离子注入混合线性离子阱 21 T FT-ICR 质谱仪的线性射频离子阱时对不需要的化学污染物进行气相离子耗尽的方法,通过消除不需要的化学噪声提高了对分析物的检测。我们展示了信噪比、动态范围和溶解有机物样品中观察到的分析物数量的改进,从而使鉴定到的分析物数量增加了 40-100%。在许多情况下,在选定的 m/z 区域,每个标称质量观测到的峰值数量增加了一倍以上。这种气相 "清理 "方法可以挽救因采样位置、样本量或采集协议而无法避免的珍贵样本,并最大限度地获得成分信息。此外,这种方法具有通用性,可扩展到任何混合线性离子阱仪器平台(如 LTQ-Orbitrap 或线性离子阱-TOF)。我们强调了电喷雾离子化气相耗竭的强大功能,但这种方法也适用于其他离子化模式。
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来源期刊
CiteScore
5.50
自引率
9.40%
发文量
257
审稿时长
1 months
期刊介绍: The Journal of the American Society for Mass Spectrometry presents research papers covering all aspects of mass spectrometry, incorporating coverage of fields of scientific inquiry in which mass spectrometry can play a role. Comprehensive in scope, the journal publishes papers on both fundamentals and applications of mass spectrometry. Fundamental subjects include instrumentation principles, design, and demonstration, structures and chemical properties of gas-phase ions, studies of thermodynamic properties, ion spectroscopy, chemical kinetics, mechanisms of ionization, theories of ion fragmentation, cluster ions, and potential energy surfaces. In addition to full papers, the journal offers Communications, Application Notes, and Accounts and Perspectives
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