Figure 3
Figure 3. Quantitative phosphoproteomic mass spectrometry identifies the global PGE2-regulated phosphoproteome. K-means clustering analysis grouping phosphopeptides with similar phosphorylation profiles after 10 and 60 minutes of PGE2 (10μM) stimulation (B). All detected phosphopeptides were depicted and color coded according to the temporal change in phosphorylation ratio in response to PGE2 (10μM) after 10 and 60 minutes, A, C, D, and A', C', D', respectively; green indicates nonregulated phosphopeptide (ratio > 0.5 and < 2); yellow, ratio > 2 regulated phosphopeptide; red, ratio > 5 regulated phosphopeptide; blue, ratio < 0.5 regulated phosphopeptide; purple, predicted kinase. Individual networks were produced showing all identified phosphopeptides (A,A'), regulated phosphopeptides only (C,C') with kinase-predicted phosphopeptides highlighted, and PKA-predicted substrates (D,D'). All networks were visualized with the use of Cytoscape (www.cytoscape.org).

Quantitative phosphoproteomic mass spectrometry identifies the global PGE2-regulated phosphoproteome. K-means clustering analysis grouping phosphopeptides with similar phosphorylation profiles after 10 and 60 minutes of PGE2 (10μM) stimulation (B). All detected phosphopeptides were depicted and color coded according to the temporal change in phosphorylation ratio in response to PGE2 (10μM) after 10 and 60 minutes, A, C, D, and A', C', D', respectively; green indicates nonregulated phosphopeptide (ratio > 0.5 and < 2); yellow, ratio > 2 regulated phosphopeptide; red, ratio > 5 regulated phosphopeptide; blue, ratio < 0.5 regulated phosphopeptide; purple, predicted kinase. Individual networks were produced showing all identified phosphopeptides (A,A'), regulated phosphopeptides only (C,C') with kinase-predicted phosphopeptides highlighted, and PKA-predicted substrates (D,D'). All networks were visualized with the use of Cytoscape (www.cytoscape.org).

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