MS/MS and LC-MS/MS analysis of choline/ethanolamine plasmalogens via promotion of alkali metal adduct formation
•MS/MS produced diagnostic ions of plasmalogen in the presence of alkali metals.•LC-MS/MS using alkali metals enabled profiling of plasmalogen molecular species.•The method easily allowed identification of plasmalogen in biological samples. Tandem mass spectrometry (MS/MS) has been used for the anal...
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Veröffentlicht in: | Journal of chromatography. B, Analytical technologies in the biomedical and life sciences Analytical technologies in the biomedical and life sciences, 2015-11, Vol.1004, p.85-92 |
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Sprache: | eng |
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Zusammenfassung: | •MS/MS produced diagnostic ions of plasmalogen in the presence of alkali metals.•LC-MS/MS using alkali metals enabled profiling of plasmalogen molecular species.•The method easily allowed identification of plasmalogen in biological samples.
Tandem mass spectrometry (MS/MS) has been used for the analysis of plasmalogen (Pls), a physiologically important class of vinyl ether-linked phospholipid. However, MS/MS generally causes little fragmentation of Pls, especially choline Pls (PC-Pls). Previous MS/MS studies reported an increased formation of product ions of PC-Pls (and also ethanolamine Pls (PE-Pls)) in the presence of ‘alkali metals.’ Therefore, use of alkali metals considerably leads to the development of a method for analysis of both PC- and PE-Pls. In this study, this notion was evaluated using quadrupole-time-of-flight MS/MS and liquid chromatography (LC) coupled with MS/MS. Results from MS/MS confirmed that alkali metals (e.g., sodium) produced significant fragmentation of PC-Pls and PE-Pls. A number of structure-diagnostic product ions exhibiting high intensities were observed under optimized MS/MS conditions using alkali metals. Moreover, the ability to selectively and sensitively identify PC-Pls and PE-Pls at the molecular species level in biological samples (rat brain and heart) was demonstrated using LC-MS/MS. Therefore, the herein developed method appears to be a powerful tool for analyzing Pls and may provide a better understanding of their physiological roles in vivo. |
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ISSN: | 1570-0232 1873-376X |
DOI: | 10.1016/j.jchromb.2015.09.012 |