RECOMBINANT HIRUDIN - KINETIC MECHANISM FOR THE INHIBITION OF HUMAN THROMBIN

被引:9
|
作者
STONE, SR
HOFSTEENGE, J
机构
[1] Friedrich Miescher-Institut, CH-4002 Basel
来源
PROTEIN ENGINEERING | 1991年 / 4卷 / 03期
关键词
HIRUDIN; KINETICS; THROMBIN;
D O I
10.1093/protein/4.3.295
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Recombinant hirudin variant-2(Lys47), was found to be a competitive inhibitor of human alpha-thrombin with respect to peptidyl p-nitroanilide substrates. These results contrast with those of Degryse and coworkers that suggest that recombinant hirudin variant-2(Lys47) inhibited thrombin by a noncompetitive mechanism [Degryse et al. (1989) Protein Engng, 2, 459-465]. gamma-Thrombin, which can arise from alpha-thrombin by autolysis, was shown to have an affinity for recombinant hirudin variant-2(Lys47) that was four orders of magnitude lower than that of alpha-thrombin. It was demonstrated that the apparent noncompetitive mechanism observed previously was probably caused by a contamination of the thrombin preparation by gamma-thrombin. Comparison of the inhibition of alpha-thrombin by recombinant hirudins variant-2(Lys47) and variant-1, which differ from one another in eight out of 65 amino acids, indicated that the two variants have essentially the same kinetic parameters.
引用
收藏
页码:295 / 300
页数:6
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