4.8 Article

Enhancing the Signal-to-Noise of Diagnostic Fragment Ions of Unsaturated Glycerophospholipids via Precursor Exclusion Ultraviolet Photodissociation Mass Spectrometry (PEx-UVPD-MS)

期刊

ANALYTICAL CHEMISTRY
卷 94, 期 32, 页码 11352-11359

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.2c02128

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资金

  1. National Institutes of Health (National Institute of General Medical Sciences of the National Institutes of Health) [R35GM139658]
  2. Welch Foundation [F-1155]
  3. UT System

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Understanding the structures and functions of lipids is important in lipidomics research. This study introduces a technique called precursor exclusion (PEx) UVPD, which improves the signal-to-noise ratio of low-abundance fragment ions obtained from UVPD of glycerophospholipids. The method allows for deeper structural analysis of lipids and confident identification of different lipid structures.
Understanding and elucidating the diverse structures and functions of lipids has motivated the development of many innovative tandem mass spectrometry (MS/MS) strategies. Higher-energy activation methods, such as ultraviolet photo- dissociation (UVPD), generate unique fragment ions from glycerophospholipids that can be used to perform in-depth structural analysis and facilitate the deconvolution of isomeric lipid structures in complex samples. Although detailed characterization is central to the correlation of lipid structure to biological function, it is often impeded by the lack of sufficient instrument sensitivity for highly bioactive but low-abundance phospholipids. Here, we present precursor exclusion (PEx) UVPD, a simple yet powerful technique to enhance the signal-to-noise (S/N) of informative low-abundance fragment ions produced from UVPD of glycerophospholipids. Through the exclusion of the large population of undissociated precursor ions with an MS3 strategy, the S/N of diagnostic fragment ions from PC 18:0/18:2(9Z, 12Z) increased up to an average of 13x for PEx-UVPD compared to UVPD alone. These enhancements were extended to complex mixtures of lipids from bovine liver extract to confidently identify 35 unique structures using liquid chromatography PEx-UVPD. This methodology has the potential to advance lipidomics research by offering deeper structure elucidation and confident identification of biologically active lipids.

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