An isotope labeling strategy for quantifying the degree of phosphorylation at multiple sites in proteins

Adrian D. Hegeman, Amy C. Harms, Michael R. Sussman, Anne E. Bunner, Jeffrey F. Harper

Research output: Contribution to journalArticlepeer-review

55 Scopus citations

Abstract

A procedure for determining the extent of phosphorylation at individual sites of multiply phosphorylated proteins was developed and applied to two polyphosphorylated proteins. The protocol, using simple chemical (Fischer methyl-esterification) and enzymatic (phosphatase) modification steps and an accessible isotopic labeling reagent (methyl alcohol-d4), is described in detail. Site-specific phosphorylation stoichiometries are derived from the comparison of chemically identical but isotopically distinct peptide species analyzed by microspray liquid chomatography-mass spectrometry (μLC-MS) using a Micromass Q-TOF2 mass spectrometer. Ten phosphorylation sites were unambiguously identified in tryptic digests of both proteins, and phosphorylation stoichiometries were determined for eight of the ten sites using the isotope-coded strategy. The extent of phosphorylation was also estimated from the mass spectral peak areas for the phosphorylated and unmodified peptides, and these estimates, when compared with stoichiometries determined using the isotope-coded technique, differed only marginally (within ∼20%).

Original languageEnglish (US)
Pages (from-to)647-653
Number of pages7
JournalJournal of the American Society for Mass Spectrometry
Volume15
Issue number5
DOIs
StatePublished - May 2004

Bibliographical note

Funding Information:
This work was supported by a grant from the National Science Foundation 2010 Project (MCB-0114769). The authors thank Drs. Catherine W. M. Chan, John C. Cushman, Alice C. Harmon, and Estelle M. Hrabak for helpful advice and valuable discussions.

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