Desorption Electrospray Ionization Coupled with Ultraviolet Photodissociation for Characterization of Phospholipid Isomers in Tissue Sections
Author(s) -
Dustin R. Klein,
Clara L. Feider,
Kyana Y. Garza,
John Q. Lin,
Lívia S. Eberlin,
Jennifer S. Brodbelt
Publication year - 2018
Publication title -
analytical chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.117
H-Index - 332
eISSN - 1520-6882
pISSN - 0003-2700
DOI - 10.1021/acs.analchem.8b03026
Subject(s) - chemistry , photodissociation , mass spectrometry , electrospray ionization , ultraviolet , mass spectrometry imaging , desorption electrospray ionization , double bond , ionization , mass spectrum , analytical chemistry (journal) , chemical ionization , photochemistry , chromatography , ion , organic chemistry , physics , quantum mechanics
Desorption electrospray ionization (DESI) mass spectrometry imaging has become a powerful strategy for analysis of tissue sections, enabling differentiation of normal and diseased tissue based on changes in the lipid profiles. The most common DESI workflow involves collection of MS1 spectra as the DESI spray is rastered over a tissue section. Relying on MS1 spectra inherently limits the ability to differentiate isobaric and isomeric species or evaluate variations in the relative abundances of key isomeric lipids, such as double-bond positional isomers which may distinguish normal and diseased tissues. Here, 193 nm ultraviolet photodissociation (UVPD), a technique capable of differentiating double-bond positional isomers, is coupled with DESI to map differences in the double-bond isomer composition in tissue sections in a fast, high throughput manner compatible with imaging applications.
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