Fig. 9.
Fig. 9. Comparison of the catalytic activity of plasma factor IXa and factor IXaR94S in the tenase enzyme complex. Plasma factor IXa (0.17 nmol/L, ○, ___) or factor IXaR94S (1.5 nmol/L, •, —-) was incubated with factor X (0 to 100 nmol/L) in the presence of phospholipid vesicles (35 μmol/L), factor VIIIa (14 U/mL) and Ca2+ (5 mmol/L) in TBS containing 0.1% BSA at 37°C. At discrete time intervals, aliquots of the reactions were quenched with 50 mmol/L EDTA and factor Xa quantitated using CHG-GR-pNA. The data has been normalized with respect to enzyme concentration by expressing the ordinate axis as initial velocity, vi, divided by the factor IXa or factor IXaR94S concentration. The lines represent the best fit of the data to the Michaelis-Menten equation using nonlinear regression analysis. The kinetic parameters are summarized in Table 1.

Comparison of the catalytic activity of plasma factor IXa and factor IXaR94S in the tenase enzyme complex. Plasma factor IXa (0.17 nmol/L, ○, ___) or factor IXaR94S (1.5 nmol/L, •, —-) was incubated with factor X (0 to 100 nmol/L) in the presence of phospholipid vesicles (35 μmol/L), factor VIIIa (14 U/mL) and Ca2+ (5 mmol/L) in TBS containing 0.1% BSA at 37°C. At discrete time intervals, aliquots of the reactions were quenched with 50 mmol/L EDTA and factor Xa quantitated using CHG-GR-pNA. The data has been normalized with respect to enzyme concentration by expressing the ordinate axis as initial velocity, vi, divided by the factor IXa or factor IXaR94S concentration. The lines represent the best fit of the data to the Michaelis-Menten equation using nonlinear regression analysis. The kinetic parameters are summarized in Table 1.

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