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Evaluation of Different Tandem MS Acquisition Modes to Support Metabolite Annotation in Human Plasma Using Ultra High-Performance Liquid Chromatography High-Resolution Mass Spectrometry for Untargeted Metabolomics

机译:不同串联MS采集模式的评价以支持人血浆中的代谢物注释使用超高效液相色谱法高分辨率质谱用于未确定的代谢组

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摘要

Ultra-high performance liquid chromatography coupled to high-resolution mass spectrometry (UHPLC-HRMS) is a powerful and essential technique for metabolite annotation in untargeted metabolomic applications. The aim of this study was to evaluate the performance of diverse tandem MS (MS/MS) acquisition modes, i.e., all ion fragmentation (AIF) and data-dependent analysis (DDA), with and without ion mobility spectrometry (IM), to annotate metabolites in human plasma. The influence of the LC separation was also evaluated by comparing the performance of MS/MS acquisition in combination with three complementary chromatographic separation modes: reversed-phase chromatography (RPLC) and hydrophilic interaction chromatography (HILIC) with either an amide (aHILIC) or a zwitterionic (zHILIC) stationary phase. RPLC conditions were first chosen to investigate all the tandem MS modes, and we found out that DDA did not provide a significant additional amount of chemical coverage and that cleaner MS/MS spectra can be obtained by performing AIF acquisitions in combination with IM. Finally, we were able to annotate 338 unique metabolites and demonstrated that zHILIC was a powerful complementary approach to both the RPLC and aHILIC chromatographic modes. Moreover, a better analytical throughput was reached for an almost negligible loss of metabolite coverage when IM-AIF and AIF using ramped instead of fixed collision energies were used.
机译:超高效液相色谱耦合到高分辨率质谱(UHPLC-HRMS)是一种强大而基本的代谢物注释在未明确的代谢物应用中的技术。本研究的目的是评估各种串联MS(MS / MS)采集模式的性能,即所有离子碎片(AIF)和数据依赖性分析(DDA),有和没有离子迁移谱图(IM),到诠释人体血浆中的代谢物。还通过将MS / MS采集的性能与三种互补色谱分离模式的组合进行比较来评估LC分离的影响:反相色谱(RPLC)和亲水性相互作用色谱(HILIC),用酰胺(肛硅)或a两倍离子(朱利品)固定阶段。首先选择RPLC条件来研究所有串联MS模式,我们发现DDA没有提供了大量的额外的化学覆盖量,并且可以通过与IM组合进行AIF采集来获得清洁器MS / MS光谱。最后,我们能够注释338个独特的代谢物,并证明朱利克是RPLC和虹柱色谱模式的强大互补方法。此外,当使用使用斜坡代替固定碰撞能量的IM-AIF和AIF时,达到了更好的分析产量,几乎可忽略的代谢物覆盖覆盖。

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