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. 2013 Mar 3;12(6):1632–1643. doi: 10.1074/mcp.M112.026161

Fig. 1.

Fig. 1.

Overview of quantitative phosphoproteome profiling. A, replication assay for WT and ΔssaR Salmonella within light and heavy labeled RAW264.7, respectively, 8 h after infection. Recovered bacteria were plated in a dilution series, and the number of CFU (colony-forming units) was determined. The mean (±S.D.) count of relative CFU was determined from three independent experiments. B, histograms of log2-transformed SILAC ratios for all phosphosites quantified from RAW264.7 (black) and HeLa (gray). Dashed lines indicate the 95% confidence interval with no experimental perturbation. C, overlap of identified (top) and regulated (bottom) proteins between RAW264.7 and HeLa.