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苯甲脒和N-丹磺酰基-(对胍基)-苯丙氨酸-哌啶(I-2581)对凝血酶酰胺水解活性抑制作用的动力学研究

Kinetic study of the inhibition of the amidolytic activity of thrombin by benzamidine and N-dansyl-(p-guanidino)-phenylalanine-piperidide (I-2581).

作者信息

Izquierdo C, Burguillo F J, Usero J L, Del Arco A

机构信息

Departamento de Química Física, Facultad de Química, Universidad deSalamanca, Spain.

出版信息

Int J Biochem. 1987;19(11):1105-12. doi: 10.1016/0020-711x(87)90313-2.

DOI:10.1016/0020-711x(87)90313-2
PMID:3428480
Abstract
  1. v([I]) data were obtained for the hydrolysis of the chromogenic substrate H-D-Phe-L-Pip-L-Arg-pNA (S-2238) by native human thrombin in the presence of the synthetic inhibitors Benzamidine and N-dansyl-(p-guanidino)-phenylalanine-piperidide (I-2581). v([S]) data were also obtained in the absence and presence of fixed concentrations of each of the inhibitors. 2. Analysis of the kinetic data was based on the numerical fitting to rate equations of the polynomial quotient type of degree n:m using nonlinear regression methods. The discrimination between rate equations with different degrees was performed by application of the statistical F test. 3. Of eight v([I]) curves fitted, in six cases it was found that degree 1:2 was significantly better than degree 1:1 at a confidence level of 95% or higher; in no case was a significant improvement found with rate equations with a higher number of parameters. For the v([S]) data, of eleven curves fitted it was found that in nine cases degree 2:2 significantly improved degree 1:1 at confidence levels 99% and in one case at a level of 95%; no significant improvement was found with rate equations of higher degree for these data either. 4. Our findings allow us to propose that inhibition of the amidolytic activity of native human thrombin by benzamidine and I-2581 may be accounted for by mechanisms whose v([I]) rate equation will be a minimum of degree 1:2, thus implying a pure inhibition.(ABSTRACT TRUNCATED AT 250 WORDS)
摘要
  1. 获得了天然人凝血酶在合成抑制剂苯甲脒和N-丹磺酰基-(对胍基)-苯丙氨酸-哌啶(I-2581)存在下对生色底物H-D-苯丙氨酸-L-哌啶-L-精氨酸-对硝基苯胺(S-2238)水解的v([I])数据。还在不存在和存在固定浓度的每种抑制剂的情况下获得了v([S])数据。2. 动力学数据的分析基于使用非线性回归方法对n:m次多项式商类型速率方程的数值拟合。通过应用统计F检验对不同次数的速率方程进行判别。3. 在拟合的八条v([I])曲线中,在六例中发现,在95%或更高的置信水平下,1:2次方程比1:1次方程拟合得显著更好;在任何情况下,参数数量更多的速率方程都没有显著改善。对于v([S])数据,在拟合的十一条曲线中,发现在九例中,2:2次方程在99%的置信水平下显著优于1:1次方程,在一例中在95%的水平下显著优于1:1次方程;对于这些数据,更高次数的速率方程也没有显著改善。4. 我们的研究结果使我们能够提出,苯甲脒和I-2581对天然人凝血酶酰胺水解活性的抑制作用可能由v([I])速率方程至少为1:2次的机制来解释,因此意味着是单纯抑制作用。(摘要截短为250字)

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1
Kinetic study of the inhibition of the amidolytic activity of thrombin by benzamidine and N-dansyl-(p-guanidino)-phenylalanine-piperidide (I-2581).苯甲脒和N-丹磺酰基-(对胍基)-苯丙氨酸-哌啶(I-2581)对凝血酶酰胺水解活性抑制作用的动力学研究
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