Nanospray Desorption Electrospray Ionization (Nano-DESI) Mass Spectrometry Imaging with High Ion Mobility Resolution

被引:14
|
作者
Jiang, Li-Xue [1 ]
Hernly, Emerson [1 ]
Hu, Hang [1 ]
Hilger, Ryan T. [1 ]
Neuweger, Heiko [2 ]
Yang, Manxi [1 ]
Laskin, Julia [1 ]
机构
[1] Purdue Univ, Dept Chem, W Lafayette, IN 47907 USA
[2] Bruker Dalton GmbH & Co, D-28359 Bremen, Germany
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
mass spectrometry imaging; trapped ion mobility spectrometry(TIMS); nanospray desorption electrospray ionization (nano-DESI); lipid isomers; high mobility resolution; BIOLOGICAL TISSUES; ADVANCEMENTS;
D O I
10.1021/jasms.3c00199
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Untargeted separationof isomeric and isobaric species in massspectrometry imaging (MSI) is challenging. The combination of ionmobility spectrometry (IMS) with MSI has emerged as an effective strategyfor differentiating isomeric and isobaric species, which substantiallyenhances the molecular coverage and specificity of MSI experiments.In this study, we have implemented nanospray desorption electrosprayionization (nano-DESI) MSI on a trapped ion mobility spectrometry(TIMS) mass spectrometer. A new nano-DESI source was constructed,and a specially designed inlet extension was fabricated to accommodatethe new source. The nano-DESI-TIMS-MSI platform was evaluated by imagingmouse brain tissue sections. We achieved high ion mobility resolutionby utilizing three narrow mobility scan windows that covered the majorityof the lipid molecules. Notably, the mobility resolution reachingup to 300 in this study is much higher than the resolution obtainedin our previous study using drift tube IMS. High-resolution TIMS successfullyseparated lipid isomers and isobars, revealing their distinct localizationsin tissue samples. Our results further demonstrate the power of high-mobility-resolutionIMS for unraveling the complexity of biomolecular mixtures analyzedin MSI experiments.
引用
收藏
页码:1798 / 1804
页数:7
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