Fig. 4.
Fig. 4. Cleavage of F.IX by HNE or F.XIa in the presence of pAB. F.IX (4.0 μmol/L) was incubated at 37°C in the presence of pAB (4.0 μmol/L) and after approximately 100 seconds, F.XIa (500 nmol/L) or HNE (400 nmol/L) was added and the incubations continued. (A) shows the fluorescence intensity values recorded for F.IX treated with F.XIa (•) or HNE (○) with excitation and emission wavelengths of 336 and 376 nm, respectively, and a cutoff filter of 350 nm in the emission beam using a Perkin Elmer LS50B Luminescence Spectrometer. (B) (F.XIa-treated F.IX) and (C) (HNE-treated F.IX) show reducing SDS-PAGE analysis of aliquots (4 μg protein each) removed from the reactions in (A) after 0, 0.5, 2, 5, 10, 20, 40, and 60 minutes of incubation with protease (lanes 1 through 8, respectively, in each case) using 5% to 20% linear polyacrylamide gradient gels after staining with Coomassie Blue. The positions of molecular weight markers (in kilodaltons) are indicated at the left of each panel.

Cleavage of F.IX by HNE or F.XIa in the presence of pAB. F.IX (4.0 μmol/L) was incubated at 37°C in the presence of pAB (4.0 μmol/L) and after approximately 100 seconds, F.XIa (500 nmol/L) or HNE (400 nmol/L) was added and the incubations continued. (A) shows the fluorescence intensity values recorded for F.IX treated with F.XIa (•) or HNE (○) with excitation and emission wavelengths of 336 and 376 nm, respectively, and a cutoff filter of 350 nm in the emission beam using a Perkin Elmer LS50B Luminescence Spectrometer. (B) (F.XIa-treated F.IX) and (C) (HNE-treated F.IX) show reducing SDS-PAGE analysis of aliquots (4 μg protein each) removed from the reactions in (A) after 0, 0.5, 2, 5, 10, 20, 40, and 60 minutes of incubation with protease (lanes 1 through 8, respectively, in each case) using 5% to 20% linear polyacrylamide gradient gels after staining with Coomassie Blue. The positions of molecular weight markers (in kilodaltons) are indicated at the left of each panel.

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