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Enzymes as molecular automata: a stochastic model of self-oscillatory glycolytic cycles in cellular metabolism

机译:作为分子自动机的酶:细胞代谢中自激糖酵解周期的随机模型

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摘要

A stochastic model based on the molecular automata approach was developed to simulate the cyclic dynamics of glycolysis-gluconcogenesis in cell energy metabolism. The stochastic algorithm, based on Gillespie's method, simulates the master equation associated with any network of enzymatically controlled reactions. This model of the glycolytic-gluconeogenetic cycle was developed by assembling the stochastic kinetic reactions controlled by two enzymes: phosphofructokinase (PFKase) and fructose-1,6-biphosphatase (FBPase). In order to obtain the hysteresis behaviour predicted by classical Sel'kov analysis, a minimum complexity is required in the allosteric regulations. This implies that the FBPase cannot have a single binding site for its transition to the inactive state (a minimum of two or three binding sites is necessary). Given the multimeric structure of this enzyme, this kinetic hypothesis is tenable. Other possible applications of the stochastic automata approach for different cases of channels, receptors and enzymatic control are suggested. (C) 2000 Elsevier Science Ireland Ltd. All rights reserved. [References: 23]
机译:建立了基于分子自动机方法的随机模型,以模拟糖酵解-糖原异生在细胞能量代谢中的循环动力学。基于吉莱斯皮(Gillespie)方法的随机算法可模拟与任何酶促反应网络相关的主方程。糖酵解-糖异生循环的模型是通过组装由两种酶控制的随机动力学反应开发的:磷酸果糖激酶(PFKase)和果糖-1,6-二磷酸酶(FBPase)。为了获得经典Sel'kov分析所预测的磁滞行为,在变构规则中要求最小的复杂度。这意味着FBPase不能具有单个结合位点以过渡到非活性状态(至少需要两个或三个结合位点)。考虑到这种酶的多聚体结构,这种动力学假设是成立的。建议使用随机自动机方法在不同情况下的通道,受体和酶促控制的其他可能应用。 (C)2000 Elsevier Science Ireland Ltd.保留所有权利。 [参考:23]

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