Suppr超能文献

协同模拟揭示了过氧化物酶化合物III的形成如何导致细胞振荡。

Concerted simulations reveal how peroxidase compound III formation results in cellular oscillations.

作者信息

Gabdoulline Razif R, Kummer Ursula, Olsen Lars F, Wade Rebecca C

机构信息

Molecular and Cellular Modeling Group, European Media Laboratory, Heidelberg, Germany.

出版信息

Biophys J. 2003 Sep;85(3):1421-8. doi: 10.1016/S0006-3495(03)74574-3.

Abstract

A major problem in mathematical modeling of the dynamics of complex biological systems is the frequent lack of knowledge of kinetic parameters. Here, we apply Brownian dynamics simulations, based on protein three-dimensional structures, to estimate a previously undetermined kinetic parameter, which is then used in biochemical network simulations. The peroxidase-oxidase reaction involves many elementary steps and displays oscillatory dynamics important for immune response. Brownian dynamics simulations were performed for three different peroxidases to estimate the rate constant for one of the elementary steps crucial for oscillations in the peroxidase-oxidase reaction, the association of superoxide with peroxidase. Computed second-order rate constants agree well with available experimental data and permit prediction of rate constants at physiological conditions. The simulations show that electrostatic interactions depress the rate of superoxide association with myeloperoxidase, bringing it into the range necessary for oscillatory behavior in activated neutrophils. Such negative electrostatic steering of enzyme-substrate association presents a novel control mechanism and lies in sharp contrast to the electrostatically-steered fast association of superoxide and Cu/Zn superoxide dismutase, which is also simulated here. The results demonstrate the potential of an integrated and concerted application of structure-based simulations and biochemical network simulations in cellular systems biology.

摘要

复杂生物系统动力学数学建模中的一个主要问题是经常缺乏动力学参数的相关知识。在此,我们基于蛋白质三维结构应用布朗动力学模拟来估计一个先前未确定的动力学参数,该参数随后用于生化网络模拟。过氧化物酶 - 氧化酶反应涉及许多基本步骤,并表现出对免疫反应很重要的振荡动力学。我们对三种不同的过氧化物酶进行了布朗动力学模拟,以估计过氧化物酶 - 氧化酶反应振荡至关重要的一个基本步骤的速率常数,即超氧化物与过氧化物酶的结合。计算得到的二级速率常数与现有实验数据吻合良好,并能预测生理条件下的速率常数。模拟结果表明,静电相互作用会降低超氧化物与髓过氧化物酶的结合速率,使其处于活化中性粒细胞振荡行为所需的范围内。酶 - 底物结合的这种负向静电引导呈现出一种新型控制机制,与超氧化物和铜锌超氧化物歧化酶的静电引导快速结合形成鲜明对比,本文也对后者进行了模拟。结果证明了基于结构的模拟和生化网络模拟在细胞系统生物学中综合协同应用的潜力。

相似文献

本文引用的文献

6
Oscillatory dynamics protect enzymes and possibly cells against toxic substances.
Faraday Discuss. 2001(120):215-27; discussion 325-51. doi: 10.1039/b103076k.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验