4.8 Article

Extended Mechanism of the Plasminogen Activator Staphylokinase Revealed by Global Kinetic Analysis: 1000-fold Higher Catalytic Activity than That of Clinically Used Alteplase

期刊

ACS CATALYSIS
卷 12, 期 7, 页码 3807-3814

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acscatal.1c05042

关键词

staphylokinase; plasminogen activator; kinetic mechanism; global numerical analysis; rate-limiting step; catalytic activity; thrombolytic; fibrin

资金

  1. Ministry of Education of the Czech Republic [INBIO -CZ.02.1.01/0.0/0.0/16_026/0008451]
  2. research infrastructures RECETOX - MEYS CR [RI LM2018121, CIISB LM2018127]
  3. Technology Agency [TN01000013]
  4. European Commission [TEAMING -857560]
  5. individual grant MSCA fellowship [CZ.02.2.69/0.0/0.0/19_074/0016274]
  6. Project Internal Grant Agency of Masaryk University [CZ.02.2.69/0.0/0.0/19_073/0016943]
  7. Masaryk University [MUNI/H/1561/2018]
  8. Brno Ph.D. Talent scholarship

向作者/读者索取更多资源

This study provides a detailed understanding of the biochemical mechanism and limiting steps of the plasminogen activator staphylokinase, and determines its high catalytic activity. This knowledge is crucial for fully understanding its catalytic functionality and designing rational engineering strategies.
The plasminogen activator staphylokinase is a fibrin-specific thrombolytic biomolecule and an attractive target for the development of effective myocardial infarction and stroke therapy. To engineer the protein rationally, a detailed understanding of the biochemical mechanism and limiting steps is essential. Conventional fitting to equations derived on the basis of simplifying approximations may be inaccurate for complex mechanisms such as that of staphylokinase. We employed a modern numerical approach of global kinetic data analysis whereby steady-state kinetics and binding affinity data sets were analyzed in parallel. Our approach provided an extended, revised understanding of the staphylokinase mechanism without simplifying approximations and determined the value of turnover number k(cat) of 117 s(-1) that was 10000-fold higher than that reported in the literature. The model further showed that the rate-limiting step of the catalytic cycle is binding of staphylokinase to plasmin molecules, which occurs via an induced-fit mechanism. The overall staphylokinase effectivity is further influenced by the formation of an inactive staphylokinase.plasminogen complex. Here, we describe a quick and simplified guide for obtaining reliable estimates of key parameters whose determination is critical to fully understand the staphylokinase catalytic functionality and define rational strategies for its engineering. Our study provides an interesting example of how a global numerical analysis of kinetic data can be used to better understand the mechanism and limiting factors of complex biochemical processes. The high catalytic activity of staphylokinase (more than 1000-fold higher than that of the clinically used drug alteplase) determined herein makes this thrombolytic agent a very attractive target for further engineering.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据