Fig. 1.
Fig. 1. Determination of Ki for 2-BDB-TcAMP inhibition of cAS-PDE. (A) The initial rate of hydrolysis of cAMP was determined in triplicate and in the presence of varying concentrations of the substrate and inhibitor. The concentrations of 2-BDB-TcAMP used were 0 μmol/L (•), 5 μmol/L (▪), 10 μmol/L (▴), and 20 μmol/L (▾). The data was fit to the equation: 1/v = 1/V + Km/V[S](1 + [I]/Ki ). (B) The slope of each line was plotted against 2-BDB-TcAMP concentrations according to the equation: slope = Km/V(1 + [I]/Ki) to give a Ki value of 5.5 ± 0.4 μmol/L (SEM).

Determination of Ki for 2-BDB-TcAMP inhibition of cAS-PDE. (A) The initial rate of hydrolysis of cAMP was determined in triplicate and in the presence of varying concentrations of the substrate and inhibitor. The concentrations of 2-BDB-TcAMP used were 0 μmol/L (•), 5 μmol/L (▪), 10 μmol/L (▴), and 20 μmol/L (▾). The data was fit to the equation: 1/v = 1/V + Km/V[S](1 + [I]/Ki ). (B) The slope of each line was plotted against 2-BDB-TcAMP concentrations according to the equation: slope = Km/V(1 + [I]/Ki) to give a Ki value of 5.5 ± 0.4 μmol/L (SEM).

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