
pmid: 15336563
Isoprenoid lipids were found to be covalently linked to proteins of Arabidopsis thaliana. Their identity (polyprenols: Prenol-9-11 with Pren-10 dominating and dolichols: Dol-15-17 with Dol-16 dominating) was confirmed by means of HPLC/ESI-MS with application of the multiple reaction monitoring technique as well as metabolic labeling of Arabidopsis plants with [(3)H]mevalonate and other precursors. The occurrence of typical farnesol-, geranylgeraniol-, and phytol-modified proteins was also noted. Radioisotopic labeling allowed detection of several proteins that were covalently bound to mevalonate-derived isoprenoid alcohols. A significant portion of polyisoprenylated proteins was recovered in the cytosolic/light vesicular fraction of Arabidopsis cells upon subfractionation. Taken together our data prove that a subset of plant proteins is polyisoprenylated.
Spectrometry, Mass, Electrospray Ionization, Arabidopsis Proteins, Terpenes, Arabidopsis, Protein Prenylation, Lipid Metabolism, Chromatography, High Pressure Liquid, Protein Binding
Spectrometry, Mass, Electrospray Ionization, Arabidopsis Proteins, Terpenes, Arabidopsis, Protein Prenylation, Lipid Metabolism, Chromatography, High Pressure Liquid, Protein Binding
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