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Quantitative analysis of protein phosphorylation status and protein kinase activity on microarrays using a novel fluorescent phosphorylation sensor dye
Author(s) -
Martin Karen,
Steinberg Thomas H.,
Cooley Laurie A.,
Gee Kyle R.,
Beechem Joseph M.,
Patton Wayne F.
Publication year - 2003
Publication title -
proteomics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.26
H-Index - 167
eISSN - 1615-9861
pISSN - 1615-9853
DOI - 10.1002/pmic.200300445
Subject(s) - phosphorylation , fluorophore , protein phosphorylation , protein microarray , biochemistry , protein kinase a , peptide , chemistry , protein array analysis , dna microarray , kinase , proteomics , fluorescence , biology , gene expression , gene , physics , quantum mechanics
Abstract Ultrasensitive detection of minute amounts of phosphorylated proteins and peptides is a key requirement for unraveling many of the most important signal transduction pathways in mammalian systems. Protein microarrays are potentially useful tools for sensitive screening of global protein expression and post‐translational modifications, such as phosphorylation. However, the analysis of signaling pathways has been hampered by a lack of reagents capable of conveniently detecting the targets of protein kinases. Historically, phosphorylation detection methods have relied upon either radioisotopes ((γ‐ 32 P)ATP(γ‐ 33 P)ATP labeling) or phosphoamino acid‐selective antibodies. Both of these methods suffer from relatively well‐known shortcomings. In this study, a small molecule fluorophore phosphosensor technology is described, referred to as Pro‐Q Diamond dye, which is capable of ultrasensitive global detection and quantitation of phosphorylated amino acid residues in peptides and proteins displayed on microarrays. The utility of the fluorescent Pro‐Q Diamond phosphosensor dye technology is demonstrated using phosphoproteins and phosphopeptides as well as with protein kinase reactions performed in miniaturized microarray assay format. Instead of applying a phosphoamino acid‐selective antibody labeled with a fluorescent or enzymatic tag for detection, a small, fluorescent probe is employed as a universal sensor of phosphorylation status. The detection limit for phosphoproteins on a variety of different commercially available protein array substrates was found to be 312–625 fg, depending upon the number of phosphate residues. Characterization of the enzymatic phosphorylation of immobilized peptide targets with Pro‐Q Diamond dye readily permits differentiation between specific and non‐specific peptide labeling at picogram to subpicogram levels of detection sensitivity.