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基于长路径长度结构的异构体离子迁移分离用于无损离子操纵与质谱联用

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

作者信息

Deng Liulin, Ibrahim Yehia M, Baker Erin S, Aly Noor A, Hamid Ahmed M, Zhang Xing, Zheng Xueyun, Garimella Sandilya V B, Webb Ian K, Prost Spencer A, Sandoval Jeremy A, Norheim Randolph V, Anderson Gordon A, Tolmachev Aleksey V, Smith Richard D

机构信息

Biological Sciences Division and Environmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, 902 Battelle Blvd, Richland, WA 99352 (USA).

出版信息

ChemistrySelect. 2016 Jul 1;1(10):2396-2399. doi: 10.1002/slct.201600460.

Abstract

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.

摘要

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。由于复杂样品中生物分子的化学多样性和丰度范围,多组学分析以及对全面测量覆盖范围的需求目前存在局限性。应对这些挑战的进展越来越基于快速分离、反应以及以其他方式操纵样品成分以进行质谱分析的能力。在此,我们报告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,随后进行质谱分析。这种方法为生物分子物种提供了前所未有的分辨率,同时具有更有效的离子利用效率,并且为大大改进对极少量样品的表征奠定了基础。

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