Skip to main content
. 2008 Sep 19;283(38):26047–26058. doi: 10.1074/jbc.M802617200

FIGURE 5.

FIGURE 5.

Effects of PtdInsP depletion and induction and the mutation of PtdInsP-binding site on kinetics of PM translocation of PKCα-C2. A, the RFP intensity ratio (=PM/(PM + cytosol)) of PKCα-C2-RFP, which indicates the relative abundance of the protein at PM versus cytosol, is plotted as a function of time. The plots are shown for no lipid depletion (•, Fig. 4C), PtdIns(4,5)P2 depletion (○, Fig. 4D; Inline graphic), PtdIns(3,4,5)P3 depletion (Δ, Fig. 4E; Inline graphic), and PtdIns(4,5)P2 + PtdIns(3,4,5)P3 depletion (□; Fig. 4F; Inline graphic). B, the RFP intensity ratio as a function of time is shown for no lipid induction (•, Fig. 4C), PtdIns(4,5)P2 induction (Δ, Fig. 4H, Inline graphic), and PtdIns(3,4,5)P3 induction (○, Fig. 4G, Inline graphic). C, the fluorescence intensity ratios of PKCα-C2-RFP (•) and K209A/K211A (○) co-transfected into NIH-3T3 cells (Fig. 4I) are plotted as a function of time. No lipid depletion was performed for this measurement.