Fig. 5.
Fig. 5. Determination of the kinetic parameters for nonproteolytic and thrombin-mediated dissociation of FVIII WT andARG531HIS from MoAb ESH8. MoAb ESH8 was covalently immobilized to a biosensor chip at 20 ng/mm2. FVIII WT or ARG531HIS (2.5 nmol/L) were bound to ESH8 at 1.12 ng/mm2. A resonance response of 200 Arc seconds corresponds to 1 ng of protein bound per square millimeter of the biosensor chip surface. The kinetics of FVIII WT orARG531HIS nonproteolytic dissociation from ESH8 was recorded after replacement of the ligand by dissociation buffer (at arrow). At the second arrow, thrombin (1 U/mL) was added and thrombin-mediated dissociation of the A2 subunit from immobilized dimers was followed. The koff values for nonproteolytic and thrombin-mediated dissociation were derived from dissociation kinetic curves as described under Materials and Methods.

Determination of the kinetic parameters for nonproteolytic and thrombin-mediated dissociation of FVIII WT andARG531HIS from MoAb ESH8. MoAb ESH8 was covalently immobilized to a biosensor chip at 20 ng/mm2. FVIII WT or ARG531HIS (2.5 nmol/L) were bound to ESH8 at 1.12 ng/mm2. A resonance response of 200 Arc seconds corresponds to 1 ng of protein bound per square millimeter of the biosensor chip surface. The kinetics of FVIII WT orARG531HIS nonproteolytic dissociation from ESH8 was recorded after replacement of the ligand by dissociation buffer (at arrow). At the second arrow, thrombin (1 U/mL) was added and thrombin-mediated dissociation of the A2 subunit from immobilized dimers was followed. The koff values for nonproteolytic and thrombin-mediated dissociation were derived from dissociation kinetic curves as described under Materials and Methods.

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