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-d(4)), 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 chromatography-mass spectrometry (microLC-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 approximately 20%).
MeSH Terms
Amino Acid Sequence
Arabidopsis
CDC2 Protein Kinase
Calcium-Calmodulin-Dependent Protein Kinases/chemistry
Cyclin-Dependent Kinases/chemistry
Escherichia coli
Isotope Labeling/methods
Molecular Sequence Data
Phosphorylation
Proteins/chemistry
Protozoan Proteins
Sensitivity and Specificity
Chemicals
Proteins
Protozoan Proteins
Calcium-Calmodulin-Dependent Protein Kinases
CDC2 Protein Kinase
Cyclin-Dependent Kinases
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Hegeman Adrian D
Biotechnology Center, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA. hegeman@biochem.wisc.edu
Harms Amy C
Sussman Michael R
Bunner Anne E
Harper Jeffrey F
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