Fig. 7.
Fig. 7. FVa degradation of recombinant APC variants in the presence of protein S. / To investigate the influence of protein S on the efficiency of the various APC variants in an FVa-degradation system, FVa (0.8 nM) from normal (A) or FV Leiden (B) plasma was incubated at 37°C for 10 minutes with increasing concentrations of the various APC variants in the presence or absence of protein S (100 nM). The remaining FVa activity was measured with the PTase assay as described in “Materials and methods.” WT APC, (○); WT APC, with human protein S (●); QGNSEDY-APC, (▵); QGNSEDY-APC with human protein S, (▴); Note the logarithmic y-axes. Each point is the mean of 2 independent experiments performed in duplicate, and the error bars represent the standard deviation.

FVa degradation of recombinant APC variants in the presence of protein S.

To investigate the influence of protein S on the efficiency of the various APC variants in an FVa-degradation system, FVa (0.8 nM) from normal (A) or FV Leiden (B) plasma was incubated at 37°C for 10 minutes with increasing concentrations of the various APC variants in the presence or absence of protein S (100 nM). The remaining FVa activity was measured with the PTase assay as described in “Materials and methods.” WT APC, (○); WT APC, with human protein S (●); QGNSEDY-APC, (▵); QGNSEDY-APC with human protein S, (▴); Note the logarithmic y-axes. Each point is the mean of 2 independent experiments performed in duplicate, and the error bars represent the standard deviation.

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