Proton Bridging in the Interactions of Thrombin with Small Inhibitors

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Kovach I. M. , Kelley P., Eddy C., Jordan F., Baykal A. T.

BIOCHEMISTRY, vol.48, no.30, pp.7296-7304, 2009 (Journal Indexed in SCI) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 48 Issue: 30
  • Publication Date: 2009
  • Doi Number: 10.1021/bi900098s
  • Title of Journal : BIOCHEMISTRY
  • Page Numbers: pp.7296-7304


Thrombin is the pivotal serine protease enzyme in the blood cascade system. Phe-Pro-Arg-chloromethylketone (PPACK), phosphate, and phosphonate ester inhibitors form a covalent bond with the active-site Ser of thrombin. PPACK, a mechanism-based inhibitor, and the phosphate/phosphonate esters form adducts that mimic intermediates formed in reactions catalyzed by thrombin. Therefore, the dependence of the inhibition of human alpha-thrombin on the concentration of these inhibitors, pH, And temperature was investigated. The second-order rate constant (k(i)/K-i) and the inhibition constant (K-i) for inhibition of human alpha-thrombin by PPACK are (1.1 +/- 0.2) x 10(7) M-1 s(-1) and (2.4 +/- 1.3) x 10(-8) M, respectively, at pH 7.00 in 0.05 M phosphate buffer and 0.15 M NaCl at 25.0 +/- 0.1 degrees C, in good agreement with previous reports. The activation parameters at pH 7.00 in 0.05 M phosphate buffer and 0.15 M NaCl are as follows: Delta H double dagger = 10.6 +/- 0.7 kcal/mol, and Delta S double dagger = 9 +/- 2 cal mol(-1) degrees C-1. The pH dependence of the second-order rate constants of inhibition is bell-shaped. Values of pK(a)1 and pK(a)2 are 7.3 +/- 0.2 and 8.8 +/- 0.3, respectively, at 25.0 +/- 0.1 degrees C. A phosphate and a phosphonate ester inhibitor gave higher values, 7.8 and 8.0 for pK(a)1 and 9.3 and 8.6 for pK(a)2, respectively. They inhibit thrombin more than 6 orders of magnitude less efficiently than PPACK does. The deuterium solvent isotope effect for the second-order rate constant at pH 7.0 and 8.3 at 25.0 +/- 0.1 degrees C is unity within experimental error in all three cases, indicating the absence of proton transfer in the rate-determining step for the association of thrombin with the inhibitors, but in a 600 MHz H-1 NMR spectrum of the inhibition adduct at pH 6.7 and 30 degrees C, a peak at 18.10 ppm with respect to TSP appears with PPACK, which is absent in the H-1 NMR spectrum of a solution of the enzyme between pH 5.3 and 8.5. The peak at low field is an indication of the presence of a short-strong hydrogen bond (SSHB) at the active site in the adduct. The deuterium isotope effect on this hydrogen bridge is 2.2 +/- 0.2 (phi = 0.45). The presence of ail SSHB is also established with a signal at 17.34 ppm for a dealkylated phosphate adduct of thrombin.