Figure 4
Figure 4. Recombinant mFVIIa chimeras bind to msEPCR in contrast to mFVIIa. Isothermal titration calorimetry was used to study the interaction of (A) mFVIIa, (B) mFVIIa-FMR, and (C) mFVIIa-(1-43 mPC) with msEPCR. Upper portion of each panel: heat flow tracings were obtained upon successive injections (2 µL) of msEPCR into the sample cell containing 25 µM mFVIIa or mFVIIa chimeras in dialysate at 25°C. The first injection (0.5 µL) was eliminated from the analysis. The heat flow profile from an identical injection of msEPCR into dialysate was used as a reference and is shown offset (top of upper panel) for clarity. Bottom portion of each panel: corrected integrated heats (kilocalories per mole of injectant) were analyzed. The line is drawn according to parameters listed in Table 1.

Recombinant mFVIIa chimeras bind to msEPCR in contrast to mFVIIa. Isothermal titration calorimetry was used to study the interaction of (A) mFVIIa, (B) mFVIIa-FMR, and (C) mFVIIa-(1-43 mPC) with msEPCR. Upper portion of each panel: heat flow tracings were obtained upon successive injections (2 µL) of msEPCR into the sample cell containing 25 µM mFVIIa or mFVIIa chimeras in dialysate at 25°C. The first injection (0.5 µL) was eliminated from the analysis. The heat flow profile from an identical injection of msEPCR into dialysate was used as a reference and is shown offset (top of upper panel) for clarity. Bottom portion of each panel: corrected integrated heats (kilocalories per mole of injectant) were analyzed. The line is drawn according to parameters listed in Table 1.

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