Abstract
Shotgun lipidomics offers fast and reproducible identification and quantification of lipids in clinical samples. Lipid extraction procedures based on the methyl tert-butyl protocol are well established for performing shotgun lipidomics in biomedical research. Here, we describe a shotgun lipidomics workflow that is well suited for the analysis of clinical samples such as tissue samples, blood plasma, and peripheral blood mononuclear cells.
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Abbreviations
- CE:
-
Cholesteryl ester
- Cer:
-
Ceramide
- DAG:
-
Diacylglycerol
- FT-ICR:
-
Fourier transform ion cyclotron resonance
- HexCer:
-
Hexosyl ceramide
- LPC:
-
Lysophosphatidylcholine
- MAG:
-
Monoacylglycerol
- MFQL:
-
Molecular fragmentation query language
- MS:
-
Mass spectrometry
- MS2:
-
Tandem mass spectrometry
- MTBE:
-
Methyl tert-butyl ether (UPAC, tert-butyl methyl ether)
- PC:
-
Phosphatidylcholine
- PE:
-
Phosphatidylethanolamine
- PG:
-
Phosphatidylglycerol
- PI:
-
Phosphatidylinositol
- PS:
-
Phosphatidylserine
- TAG:
-
Triacylglycerol
- TOF:
-
Time of flight
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Acknowledgments
The research was supported by funds of the EXC 306 Inflammation at Interfaces, German Centre for Infection Research (DZIF TTU-TB), German Centre for Lung Research, Airway Research Center North (ARCN), and Lipidomics Informatics for Life-Sciences (LIFS) of the German Network for Bioinformatics Infrastructure (de.NBI).
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Eggers, L.F., Schwudke, D. (2018). Shotgun Lipidomics Approach for Clinical Samples. In: Giera, M. (eds) Clinical Metabolomics. Methods in Molecular Biology, vol 1730. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4939-7592-1_12
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DOI: https://doi.org/10.1007/978-1-4939-7592-1_12
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