Integrating Ion Mobility Spectrometry and Mass Spectrometry Imaging for Characterizing the Distribution of Biologically Active Disaccharide Isomers.

IF 2.7 2区 化学 Q2 BIOCHEMICAL RESEARCH METHODS
Ting Zeng, Xueyun Zheng, Kevin Zemaitis, Dušan Veličković, Christopher R Anderton
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Abstract

The ability to differentiate disaccharide isomers within plant tissues, in a spatially resolved fashion, is required to render a more precise understanding of their biological function within these systems. In this study, we report drift tube ion mobility spectrometry (DTIMS) and trapped ion mobility spectrometry (TIMS) profiling of two important plant disaccharides, sucrose and trehalose, along with their 6-phosphate derivatives. We then map these disaccharides in poplar root and soybean root nodules using matrix-assisted laser desorption/ionization (MALDI) mass spectrometry imaging (MSI) with premass analysis TIMS. This approach bridged an analytical gap for the straightforward visualization and discrimination of disaccharides within plant tissues at a spatial resolutions approaching a single plant cell size. We found direct infusion DTIMS and TIMS MS worked congruently to obtain the collision cross section (CCS) values of disaccharides, where we measured ΔCCS < 1.5% between DTCCSN2 and TIMSCCSN2 across all ions compared. This approach provided a baseline comparison for subsequent MSI measurements. We observed the disaccharide ion at m/z 381.08 ([M + K]+) displayed a single CCS value in poplar roots, whereas two different CCS values were measurable in soybean root nodules, which exemplified coexisting disaccharide isomers in this plant root tissue. We found the high-resolution ion mobility fingerprinting and ion imaging for the disaccharide isomer 6-phosphate derivatives in plant tissues were more challenging compared to those for the nonphosphorylated disaccharide species. This may be in part due to their lower abundance and MALDI-induced in-source fragmentation. Empowered by the integration of ion mobility spectrometry and MSI, this study provides a new avenue for easier characterization and direct visualization of disaccharide isomers within plant tissue.

结合离子迁移率光谱和质谱成像表征生物活性双糖异构体的分布。
在植物组织中,以空间分辨的方式区分双糖异构体的能力,是对它们在这些系统中的生物学功能进行更精确理解所必需的。在这项研究中,我们报告了两种重要的植物双糖,蔗糖和海藻糖及其6-磷酸衍生物的漂移管离子迁移率光谱(DTIMS)和捕获离子迁移率光谱(TIMS)分析。然后,我们利用基质辅助激光解吸/电离(MALDI)质谱成像(MSI)和质前分析TIMS在杨树根和大豆根瘤中绘制了这些双糖。这种方法弥补了在接近单个植物细胞大小的空间分辨率下植物组织中直接可视化和区分双糖的分析差距。我们发现直接输注DTIMS和TIMS MS在获得双糖的碰撞截面(CCS)值方面是一致的,在所有离子的比较中,我们测量到DTCCSN2和TIMSCCSN2之间的ΔCCS < 1.5%。这种方法为随后的MSI测量提供了基线比较。我们观察到双糖离子在m/z 381.08 ([m + K]+)处呈现单一CCS值,而在大豆根瘤中可测量到两个不同的CCS值,这说明该植物根组织中存在双糖异构体。我们发现,与非磷酸化的双糖相比,植物组织中6-磷酸二糖异构体衍生物的高分辨率离子迁移率指纹图谱和离子成像更具挑战性。这可能部分是由于它们的丰度较低和maldi引起的源内破碎。通过离子迁移谱法和MSI的整合,本研究为植物组织中双糖异构体的更容易表征和直接可视化提供了新的途径。
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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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