Draculin, the anticoagulant factor in vampire bat saliva, is a tight-binding, noncompetitive inhibitor of activated factor X. Biochim. Biophys.

Citation

Material Information

Title:
Draculin, the anticoagulant factor in vampire bat saliva, is a tight-binding, noncompetitive inhibitor of activated factor X. Biochim. Biophys.
Series Title:
Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology
Creator:
Fernandez, Ana Z.
Tablante, Alfonso
Beguin, Suzette
Hemker, H.C.
Apitz-Castro, Rafael
Publisher:
Elsevier
Publication Date:
Language:
English

Subjects

Subjects / Keywords:
Fxa Inhibition ( local )
Draculin ( local )
Tight-Binding Inhibitor ( local )
Natural Anticoagulant ( local )
(Vampire Bat) ( local )
Genre:
serial ( sobekcm )

Notes

Abstract:
The kinetic mechanism of action of Draculin on activated Factor X (FXa) is established. Draculin inhibits activated Factor X within seconds of incubation at near equimolar concentration (2–6 times on molar basis). Fitting the data to the equation for a tight-binding inhibitor gives a value for Ki(Kd)=14.8±1.5 nM. The formation of the Draculin–FXa complex can be explained by a two-step mechanism, where for the first, reversible step, kon=1.117 (±0.169, S.E.M.)×106 M−1 s−1 and koff=15.388 (±1.672)×10−3 s−1, while for the second, irreversible step, which is concentration-independent, k2=0.072 s−1. Kd obtained from koff/kon=13.76 nM. Lineweaver–Burk plot shows a noncompetitive behavior. This noncompetitive mode of inhibition of Draculin is supported by the observation that Draculin, at concentrations giving complete inhibition, does not impair binding of p-aminobenzamidine to FXa. Moreover, under the same conditions, Draculin induces <14% decrease of the fluorescence intensity of the p-aminobenzamidine–FXa complex. We conclude that Draculin is a noncompetitive, tight-binding inhibitor of FXa, a characteristic so far unique amongst natural FXa inhibitors.
Original Version:
Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology, Vol. 1434, no. 1 (1999-09-14).

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