Automated monitoring of phosphatidylcholine biosyntheses in Plasmodium falciparum by electrospray ionization mass spectrometry, through stable isotope labeling experiments
被引:12
作者:
Enjalbal, C
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机构:Univ Montpellier 2, UMR 5810, Lab Aminoacides Peptides & Prot, F-34095 Montpellier 05, France
Enjalbal, C
Roggero, R
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机构:Univ Montpellier 2, UMR 5810, Lab Aminoacides Peptides & Prot, F-34095 Montpellier 05, France
Roggero, R
Cerdan, R
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机构:Univ Montpellier 2, UMR 5810, Lab Aminoacides Peptides & Prot, F-34095 Montpellier 05, France
Cerdan, R
Martinez, J
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机构:Univ Montpellier 2, UMR 5810, Lab Aminoacides Peptides & Prot, F-34095 Montpellier 05, France
Martinez, J
Vial, H
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机构:Univ Montpellier 2, UMR 5810, Lab Aminoacides Peptides & Prot, F-34095 Montpellier 05, France
Vial, H
Aubagnac, JL
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机构:Univ Montpellier 2, UMR 5810, Lab Aminoacides Peptides & Prot, F-34095 Montpellier 05, France
Aubagnac, JL
机构:
[1] Univ Montpellier 2, UMR 5810, Lab Aminoacides Peptides & Prot, F-34095 Montpellier 05, France
[2] Univ Montpellier 2, F-34095 Montpellier 05, France
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.