期刊
ANALYTICAL CHEMISTRY
卷 93, 期 13, 页码 5468-5475出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.0c05145
关键词
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资金
- NSF
- NASA Astrobiology Program under the NSF Center for Chemical Evolution [CHE-1504217]
- NIH [1R01CA2186 6 4 -0 1, 1U2CES030167-01, 1U24DK112341]
- CMaT NSF Research Center [EEC1648035]
This study demonstrated the successful structural characterization and annotation of lipids using large-area triboelectric nanogenerators combined with time-aligned parallel fragmentation mass spectrometry analysis, providing detailed information on double bonds, sn-chain positions, and C=C isomerism. This methodology offers a new avenue for lipid analysis in biological samples.
Lipids play a critical role in cell membrane integrity, signaling, and energy storage. However, in-depth structural characterization of lipids is still challenging and not routinely possible in lipidomics experiments. Techniques such as collision-induced dissociation (CID) tandem mass spectrometry (MS/MS), ion mobility (IM) spectrometry, and ultrahigh-performance liquid chromatography are not yet capable of fully characterizing double-bond and sn-chain position of lipids in a high-throughput manner. Herein, we report on the ability to structurally characterize lipids using large-area triboelectric nanogenerators (TENG) coupled with time-aligned parallel (TAP) fragmentation IM-MS analysis. Gas-phase lipid epoxidation during TENG ionization, coupled to mobility-resolved MS3 via TAP IM-MS, enabled the acquisition of detailed information on the presence and position of lipid C=C double bonds, the fatty acyl sn-chain position and composition, and the cis/trans geometrical C=C isomerism. The proposed methodology proved useful for the shotgun lipidomics analysis of lipid extracts from biological samples, enabling the detailed annotation of numerous lipid isobars.
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