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Analysis of the Amine Submetabolome Using Novel Isotope-Coded Pyrylium Salt Derivatization and LC-MS: Herbs and Cancer Tissues as Cases

Authors :
Liu, Li
Bao, Geng-Yu
Zhang, Shu-Sheng
Qin, Yong
Chen, Xiu-Ping
Wang, Ming-Dan
Zhu, Jian-Ping
Yin, Hang
Lin, Guo-Qiang
Feng, Chen-Guo
Zhang, Fang
Guo, Yin-Long
Source :
Analytical Chemistry; December 2022, Vol. 94 Issue: 50 p17606-17615, 10p
Publication Year :
2022

Abstract

The amine submetabolome, including amino acids (AAs) and biogenic amines (BAs), is a class of small molecular compounds exhibiting important physiological activities. Here, a new pyrylium salt named 6,7-dimethoxy-3-methyl isochromenylium tetrafluoroborate ([d0]-DMMIC) with stable isotope-labeled reagents ([d3]-/[d6]-DMMIC) was designed and synthesized for amino compounds. [d0]-/[d3]-/[d6]-DMMIC-derivatized had a charged tag and formed a set of molecular ions with an increase of 3.02 m/zand the characteristic fragment ions of m/z204.1:207.1:210.1. When DMMIC coupled with liquid chromatography-mass spectrometry (LC-MS), a systematic methodology evaluation for quantitation proved to have good linearity (R2between 0.9904 and 0.9998), precision (interday: 2.2–21.9%; intraday: 1.0–19.7%), and accuracy (recovery: 71.8–108.8%) through the test AAs. Finally, the methods based on DMMIC and LC-MS demonstrated the advantaged application by the nontargeted screening of BAs in a common medicinal herb Senecio scandensand an analysis of metabolic differences among the amine submetabolomes between the carcinoma and paracarcinoma tissues of esophageal squamous cell carcinoma (ESCC). A total of 20 BA candidates were discovered in S. scandensas well as the finding of 13 amine metabolites might be the highest-potential differential metabolites in ESCC. The results showed the ability of DMMIC coupled with LC-MS to analyze the amine submetabolome in herbs and clinical tissues.

Details

Language :
English
ISSN :
00032700 and 15206882
Volume :
94
Issue :
50
Database :
Supplemental Index
Journal :
Analytical Chemistry
Publication Type :
Periodical
Accession number :
ejs61272130
Full Text :
https://doi.org/10.1021/acs.analchem.2c04246