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Ion Mobility Separations of Isomers based upon Long Path Length Structures for Lossless Ion Manipulations Combined with Mass Spectrometry

机译:基于长路径长度结构的异构体的离子淌度分离结合质谱用于无损离子处理

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摘要

Mass spectrometry (MS)-based multi-omic measurements, including proteomics, metabolomics, lipidomics, and glycomics, are increasingly transforming our ability to characterize and understand biological systems. Multi-omic analyses and the desire for comprehensive measurement coverage presently have limitations due to the chemical diversity and range of abundances of biomolecules in complex samples. Advances addressing these challenges increasingly are based upon the ability to quickly separate, react and otherwise manipulate sample components for analysis by MS. Here we report on a new approach using Structures for Lossless Ion Manipulations (SLIM) to enable long serpentine path ion mobility spectrometry (IMS) separations followed by MS analyses. This approach provides previously unachieved resolution for biomolecular species, in conjunction with more effective ion utilization, and a basis for greatly improved characterization of very small sample sizes.
机译:基于质谱(MS)的多组学测量,包括蛋白质组学,代谢组学,脂质组学和糖组学,正在日益改变我们表征和理解生物系统的能力。由于复杂样品中化学分子的多样性和生物分子的丰度范围,多组学分析和对全面测量范围的需求目前存在局限性。迅速解决这些挑战的进步基于快速分离,反应和操纵样品成分进行质谱分析的能力。在这里,我们报告了一种使用无损离子操纵结构(SLIM)的新方法,以实现长蛇形路径离子迁移谱(IMS)分离,然后进行MS分析。这种方法结合了更有效的离子利用,为生物分子提供了以前无法实现的分离度,并为大大提高非常小的样品尺寸的表征提供了基础。

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