Abstract
Glycerophospholipids are a highly abundant and diverse collection of biologically relevant lipids, and distinction between isomeric and isobaric species is a fundamental aspect for confident identification. The ability to confidently assign a unique structure to a glycerophospholipid of interest is dependent on determining the number and location of the points of unsaturation and assignment of acyl chain position. The use of high-energy electrons (>20 eV) to induce gas-phase dissociation of intact precursor ions results in diagnostic product ions for localizing double-bond positions and determining acyl chain assignment. We describe a high-resolution, tandem mass spectrometry method for structure characterization of glycerophospholipids using electron-induced dissociation (EID). Furthermore, the inclusion of nomenclature to systematically assign bond cleavage sites with acyl chain position and double-bond location enables a uniform platform for lipid identification. The EID methodology detailed here combines novel application of an electron-based dissociation technique with high-resolution mass spectrometry that facilitates a new experimental approach for lipid biomarker discovery and validation.
| Original language | English |
|---|---|
| Pages (from-to) | 1327-1339 |
| Number of pages | 13 |
| Journal | Journal of Mass Spectrometry |
| Volume | 50 |
| Issue number | 12 |
| DOIs | |
| State | Published - 1 Dec 2015 |
Keywords
- electron-induced dissociation
- FT-ICR
- lipidomics
- tandem mass spectrometry
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