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. 2011 Feb 1;286(14):12702–12711. doi: 10.1074/jbc.M110.166538

FIGURE 7.

FIGURE 7.

Effects of R* and β1γ1 on PDE activation by αT* (S43N). αT*(S43N) bound to GTPγS was prepared as described in Fig. 6B. This was diluted in AB buffer to a final concentration of 250 nm. Subsequently, the β1γ1 subunit complex (500 nm, panel A) or R* (4.8 μm, panel B) was added to the sample in the presence of varying concentrations of R* (panel A) or β1γ1 (panel B). PDE was added to a final concentration of 160 nm, and its activation was measured as described for Fig. 6B.