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Expanding lipidomics coverage: effective ultra performance liquid chromatography-high resolution mass spectrometer methods for detection and quantitation of cardiolipin, phosphatidylglycerol, and lysyl-phosphatidylglycerol

  • Tague, Eric D.1
  • Woodall, Brittni M.1, 2
  • Harp, John R.3
  • Farmer, Abigail T.1
  • Fozo, Elizabeth M.3
  • Campagna, Shawn R.1, 4
  • 1 University of Tennessee, Department of Chemistry, Knoxville, TN, 37996, USA , Knoxville (United States)
  • 2 University of Tennessee, Department of Biochemistry & Cellular and Molecular Biology, Knoxville, TN, 37996, USA , Knoxville (United States)
  • 3 University of Tennessee, Department of Microbiology, Knoxville, TN, 37996, USA , Knoxville (United States)
  • 4 University of Tennessee, Biological and Small Mass Spectrometry Core, Knoxville, TN, 37996, USA , Knoxville (United States)
Published Article
Springer US
Publication Date
Mar 27, 2019
DOI: 10.1007/s11306-019-1512-7
Springer Nature


IntroductionLipidomics can reveal global alterations in a broad class of molecules whose functions are innately linked to physiology. Monitoring changes in the phospholipid composition of biological membranes in response to stressors can aid the development of targeted therapies. However, exact quantitation of cardiolipins is not a straightforward task due to low ionization efficiencies and poor chromatographic separation of these compounds.ObjectiveThe aim of this study was to develop a quantitative method for the detection of cardiolipins and other phospholipids using both a targeted and untargeted analyses with a Q-Exactive.MethodsHILIC chromatography and high-resolution mass spectrometry with parallel reaction monitoring was used to measure changes in lipid concentration. Internal standards and fragmentation techniques allowed for the reliable quantitation of lipid species including: lysyl-phosphatidylglycerol, phosphatidylglycerol, and cardiolipin.ResultsThe untargeted analysis was capable to detecting 6 different phospholipid classes as well as free fatty acids. The targeted analysis quantified up to 23 cardiolipins, 10 phosphatidylglycerols and 10 lysyl-phosphatidylglycerols with detection limits as low as 50 nM. Biological validation with Enterococcus faecalis demonstrates sensitivity in monitoring the incorporation of exogenously supplied free fats into membrane phospholipids. When supplemented with oleic acid, the amount of free oleic acid in the membrane was 100 times greater and the concentration of polyunsaturated cardiolipin increased to over 3.5 µM compared to controls.ConclusionsThis lipidomics method is capable of targeted quantitation for challenging biologically relevant cardiolipins as well as broad, untargeted lipid profiling.

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