Suppr超能文献

组织因子途径生成凝血酶的模型。II. 数学模拟。

A model for the tissue factor pathway to thrombin. II. A mathematical simulation.

作者信息

Jones K C, Mann K G

机构信息

Department of Biochemistry, University of Vermont, College of Medicine, Burlington 05405-0068.

出版信息

J Biol Chem. 1994 Sep 16;269(37):23367-73.

PMID:8083242
Abstract

A mathematical simulation of the tissue factor pathway to the generation of thrombin has been developed using a combination of empirical, estimated, and deduced rate constants for reactions involving the activation of factor IX, X, V, and VIII, in the formation of thrombin, as well as rate constants for the assembly of the coagulation enzyme complexes which involve factor VIIIa-factor IXa (intrinsic tenase) and factor Va-Xa (prothrombinase) assembled on phospholipid membrane. Differential equations describing the fate of each species in the reaction were developed and solved using an interactive procedure based upon the Runge-Kutta technique. In addition to the theoretical considerations involving the reactions of the tissue factor pathway, a physical constraint associated with the stability of the factor VIIIa-factor IXa complex has been incorporated into the model based upon the empirical observations associated with the stability of this complex. The model system provides a realistic accounting of the fates of each of the proteins in the coagulation reaction through a range of initiator (factor VIIa-tissue factor) concentrations ranging from 5 pM to 5 nM. The model is responsive to alterations in the concentrations of factor VIII, factor V, and their respective activated species, factor VIIIa and factor Va, and overall provides a reasonable approximation of empirical data. The computer model permits the assessment of the reaction over a broad range of conditions and provides a useful tool for the development and management of reaction studies.

摘要

利用经验、估计和推导的反应速率常数相结合的方法,建立了一个从组织因子途径到凝血酶生成的数学模拟模型。这些反应速率常数涉及因子IX、X、V和VIII的激活、凝血酶的形成,以及涉及在磷脂膜上组装的凝血酶原酶复合物(包括因子VIIIa - 因子IXa(内源性凝血酶原酶)和因子Va - Xa(凝血酶原酶))的组装速率常数。利用基于龙格 - 库塔技术的交互式程序,建立并求解了描述反应中各物质命运轨迹的微分方程。除了涉及组织因子途径反应的理论考量外,基于与因子VIIIa - 因子IXa复合物稳定性相关的经验观察,还将与该复合物稳定性相关的物理约束纳入了模型。该模型系统通过一系列起始剂(因子VIIa - 组织因子)浓度范围从5 pM到5 nM,对凝血反应中每种蛋白质的命运进行了真实的描述。该模型对因子VIII、因子V及其各自的活化形式因子VIIIa和因子Va的浓度变化有响应,总体上对实验数据提供了合理的近似。该计算机模型允许在广泛的条件下评估反应,并为反应研究的开展和管理提供了一个有用的工具。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验