Automated Monitoring of Phosphatidylcholine Biosyntheses in Plasmodium falciparum by Electrospray Ionization Mass Spectrometry through Stable Isotope Labeling Experiments
The metabolic pathways contributing to phosphatidylcholine biosyntheses in Plasmodium falciparum, the malaria-causing parasite, was explored by electrospray ionization mass spectrometry. Phosphatidylcholine produced by the CDP-choline pathway and by the methylation of phosphatidylethanolamine was id...
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Veröffentlicht in: | Analytical chemistry (Washington) 2004-08, Vol.76 (15), p.4515-4521 |
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creator | ENJALBAL, Christine ROGGERO, Rodolphe CERDAN, Rachel MARTINEZ, Jean VIAL, Henri AUBAGNAC, Jean-Louis |
description | The metabolic pathways contributing to phosphatidylcholine biosyntheses in Plasmodium falciparum, the malaria-causing parasite, was explored by electrospray ionization mass spectrometry. Phosphatidylcholine produced by the CDP-choline pathway and by the methylation of phosphatidylethanolamine was identified and quantified through isotopic labeling experiments. A straightforward method based on cone voltage directed in-source fragmentations and relative abundance measurement of endogenous versus deuterated specific fragment ions was developed for simple and rapid automated data acquisition. Such high-throughput analytical protocol allowed us to measure the relative contribution of two different metabolic pathways leading to phosphatidylcholine without performing technically more demanding and time-consuming MS/MS or LC/MS experiments. |
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Chem</addtitle><date>2004-08-01</date><risdate>2004</risdate><volume>76</volume><issue>15</issue><spage>4515</spage><epage>4521</epage><pages>4515-4521</pages><issn>0003-2700</issn><eissn>1520-6882</eissn><coden>ANCHAM</coden><abstract>The metabolic pathways contributing to phosphatidylcholine biosyntheses in Plasmodium falciparum, the malaria-causing parasite, was explored by electrospray ionization mass spectrometry. Phosphatidylcholine produced by the CDP-choline pathway and by the methylation of phosphatidylethanolamine was identified and quantified through isotopic labeling experiments. A straightforward method based on cone voltage directed in-source fragmentations and relative abundance measurement of endogenous versus deuterated specific fragment ions was developed for simple and rapid automated data acquisition. Such high-throughput analytical protocol allowed us to measure the relative contribution of two different metabolic pathways leading to phosphatidylcholine without performing technically more demanding and time-consuming MS/MS or LC/MS experiments.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>15283596</pmid><doi>10.1021/ac049759+</doi><tpages>7</tpages></addata></record> |
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subjects | Animals Automation - methods Chromatography, Liquid Deuterium Isotopes Mass Spectrometry Metabolism Parasites Phosphatidylcholines - biosynthesis Plasmodium falciparum - metabolism Spectrometry, Mass, Electrospray Ionization |
title | Automated Monitoring of Phosphatidylcholine Biosyntheses in Plasmodium falciparum by Electrospray Ionization Mass Spectrometry through Stable Isotope Labeling Experiments |
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