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[血栓烷合成多酶系统的动力学模型及调控机制]

[Kinetic model and mechanism of regulation of a multienzyme system of thromboxane synthesis].

作者信息

Varfolomeev S D, Gachok V P, Mevkh A T

出版信息

Mol Biol (Mosk). 1985 Nov-Dec;19(6):1648-60.

PMID:3935913
Abstract

A kinetic model has been suggested for the thromboxane synthesis polyenzyme system, taking into account the inactivation of a limiting enzyme, prostaglandin H-synthetase, in the course of the reaction. The model also includes the effect of phospholipase, adenylate cyclase, as well as the "outflows" of the components from the system, and basic regulatory effects in the system. A mathematical description of the model is given, and numerical solutions of the system of equations obtained for a wide variety of parameters. An analysis of the kinetic responses of the polyenzyme system shows that: 1) the system is highly conserved with respect to thromboxane concentration changes; 2) two cardinally different modes of the system are registered; they correspond to two insignificantly differing thromboxane steady-state levels; 3) transition of the system from one mode to the other is controlled by the phospholipase activity level which is sensitive to a change in the concentration of the regulator (cyclo-AMP or Ca ions) in the system. It is presumed that the two thromboxane steady-state levels are of physiological significance.

摘要

针对血栓烷合成多酶系统,已提出一种动力学模型,该模型考虑了限速酶前列腺素H合成酶在反应过程中的失活情况。该模型还包括磷脂酶、腺苷酸环化酶的作用,以及系统中各组分的“流出”情况,以及系统中的基本调节作用。给出了该模型的数学描述,并针对各种参数得到了方程组的数值解。对多酶系统动力学响应的分析表明:1)该系统在血栓烷浓度变化方面具有高度保守性;2)记录到系统存在两种根本不同的模式;它们对应于两种差异不显著的血栓烷稳态水平;3)系统从一种模式转变为另一种模式受磷脂酶活性水平控制,而磷脂酶活性水平对系统中调节剂(环磷酸腺苷或钙离子)浓度的变化敏感。据推测,这两种血栓烷稳态水平具有生理意义。

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