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. Author manuscript; available in PMC: 2010 Nov 12.
Published in final edited form as: J Biol Chem. 2007 Oct 8;282(48):34611–34622. doi: 10.1074/jbc.M707795200

FIGURE 8. Expanded negative ion electrospray ionization mass spectra of myocardial lipid extracts from iPLA2γ KO mice and their wild type littermates.

FIGURE 8

Myocardial lipid extracts of wild type mice (A) and iPLA2γ KO mice (B) were prepared by a modified Bligh and Dyer procedure. Negative ion electrospray ionization mass spectra were acquired using a QqQ mass spectrometer as described under “Experimental Procedures.” Spectra have been normalized to a CL internal standard (see insets). The asterisks indicate the doubly charged CL plus-one isotopologues whose ion peak intensities were utilized to quantify individual CL molecular species as described previously (26). The results indicate the paucity of tetra-18:2 CL molecular species in the iPLA2γ KO in comparison with WT (compare peaks at m/z 723.5 in control versus iPLA2γ KO). The insets on the right of each panel show the extended mass spectra that display additional internal standards and other major anionic phospholipids.