Quantitation of changes in protein phosphorylation: A simple method based on stable isotope labeling and mass spectrometry

Débora Bonenfant, Tobias Schmelzle, Estela Jacinto, José L. Crespo, Thierry Mini, Michael N. Hall, Paul Jenoe

Research output: Contribution to journalArticle

99 Citations (Scopus)

Abstract

Reversible protein phosphorylation plays an important role in many cellular processes. However, a simple and reliable method to measure changes in the extent of phosphorylation is lacking. Here, we present a method to quantitate the changes in phosphorylation occurring in a protein in response to a stimulus. The method consists of three steps: (i) enzymatic digestion in H216O or isotopically enriched H218O to label individual pools of differentially phosphorylated proteins; (ii) affinity selection of phosphopeptides from the combined digests by immobilized metal-affinity chromatography; and (iii) dephosphorylation with alkaline phosphatase to allow for quantitation of changes of phosphorylation by matrixassisted laser desorption ionization time-of-flight mass spectrometry. We applied this strategy to the analysis of the yeast nitrogen permease reactivator protein kinase involved in the target of rapamycin signaling pathway. Alteration in the extent of phosphorylation at Ser-353 and Ser-357 could be easily assessed and quantitated both in wild-type yeast cells treated with rapamycin and in cells lacking the SIT4 phosphatase responsible for dephosphorylating nitrogen permease reactivator protein. The method described here is simple and allows quantitation of relative changes in the level of phosphorylation in signaling proteins, thus yielding information critical for understanding the regulation of complex protein phosphorylation cascades.

Original languageEnglish (US)
Pages (from-to)880-885
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Volume100
Issue number3
DOIs
StatePublished - Feb 4 2003

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Isotope Labeling
Mass Spectrometry
Phosphorylation
Proteins
Membrane Transport Proteins
Sirolimus
Nitrogen
Yeasts
Phosphopeptides
Affinity Chromatography
Phosphoric Monoester Hydrolases
Protein Kinases
Alkaline Phosphatase
Digestion
Lasers
Metals

All Science Journal Classification (ASJC) codes

  • General

Cite this

Bonenfant, Débora ; Schmelzle, Tobias ; Jacinto, Estela ; Crespo, José L. ; Mini, Thierry ; Hall, Michael N. ; Jenoe, Paul. / Quantitation of changes in protein phosphorylation : A simple method based on stable isotope labeling and mass spectrometry. In: Proceedings of the National Academy of Sciences of the United States of America. 2003 ; Vol. 100, No. 3. pp. 880-885.
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Quantitation of changes in protein phosphorylation : A simple method based on stable isotope labeling and mass spectrometry. / Bonenfant, Débora; Schmelzle, Tobias; Jacinto, Estela; Crespo, José L.; Mini, Thierry; Hall, Michael N.; Jenoe, Paul.

In: Proceedings of the National Academy of Sciences of the United States of America, Vol. 100, No. 3, 04.02.2003, p. 880-885.

Research output: Contribution to journalArticle

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