Temporal Analysis of Sucrose-induced Phosphorylation Changes in Plasma Membrane Proteins of Arabidopsis

• Published in: Molecular & cellular proteomics Vol. 6; no. 10; pp. 1711 - 1726
• Main Authors: Niittylä, Totte, Fuglsang, Anja T., Palmgren, Michael G., Frommer, Wolf B., Schulze, Waltraud X.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.10.2007; American Society for Biochemistry and Molecular Biology
• Subjects: Amino Acid Sequence; Aquaporins - metabolism; Arabidopsis - cytology; Arabidopsis - drug effects; Arabidopsis - enzymology; Arabidopsis - metabolism; Arabidopsis Proteins - chemistry; Arabidopsis Proteins - isolation & purification; Arabidopsis Proteins - metabolism; Cell Membrane - drug effects; Cell Membrane - enzymology; Cell Membrane - metabolism; Cluster Analysis; Mass Spectrometry; Membrane Transport Proteins - metabolism; Molecular Sequence Data; Phosphopeptides - chemistry; Phosphopeptides - isolation & purification; Phosphopeptides - metabolism; Phosphorylation - drug effects; Plant Proteins - metabolism; Plasma Membrane Calcium-Transporting ATPases - metabolism; Protein Kinases - metabolism; Proton-Translocating ATPases - metabolism; Seedlings - drug effects; Seedlings - metabolism; Substrate Specificity - drug effects; Sucrose - pharmacology; Time Factors
• ISSN: 1535-9476; 1535-9484
• DOI: 10.1074/mcp.M700164-MCP200

Sucrose is the main product of photosynthesis and the most common transport form of carbon in plants. In addition, sucrose is a compound that serves as a signal affecting metabolic flux and development. Here we provide first results of externally induced phosphorylation changes of plasma membrane proteins in Arabidopsis. In an unbiased approach, seedlings were grown in liquid medium with sucrose and then depleted of carbon before sucrose was resupplied. Plasma membranes were purified, and phosphopeptides were enriched and subsequently analyzed quantitatively by mass spectrometry. In total, 67 phosphopeptides were identified, most of which were quantified over five time points of sucrose resupply. Among the identified phosphorylation sites, the well described phosphorylation site at the C terminus of plasma membrane H+-ATPases showed a relative increase in phosphorylation level in response to sucrose. This corresponded to a significant increase of proton pumping activity of plasma membrane vesicles from sucrose-supplied seedlings. A new phosphorylation site was identified in the plasma membrane H+-ATPase AHA1 and/or AHA2. This phosphorylation site was shown to be crucial for ATPase activity and overrode regulation via the well known C-terminal phosphorylation site. Novel phosphorylation sites were identified for both receptor kinases and cytosolic kinases that showed rapid increases in relative intensities after short times of sucrose treatment. Seven response classes were identified including non-responsive, rapid increase (within 3 min), slow increase, and rapid decrease. Relative quantification of phosphorylation changes by phosphoproteomics provides a means for identification of fast responses to external stimuli in plants as a basis for further functional characterization.