热休克后sumo酰化的数据驱动模型

Manyu Zhang, Yifei Zhang, Alice Zhao, Chun Guo, Lingzhong Guo
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引用次数: 0

摘要

在生物医学系统中,了解细胞在暴露于极端压力(如热休克)时如何决定命运是至关重要的。人们早就知道,细胞暴露在高温下通常会通过热休克反应(HSR)来保护自己,其中变性或未折叠的蛋白质的积累通过热休克转录因子(例如热休克因子1 (HSF1))触发热休克蛋白(HSPs)的合成。最近的实验工作也表明,蛋白质翻译后修饰(PTMs)如SUMOylation在细胞对热休克的反应中起着至关重要的作用。作为对现有实验方法的补充,在本研究中,我们旨在建立高铁的summoyla -development synergistic数学模型,以定量研究高铁的动力学行为。动力学模型的结构主要由质量作用动力学推导而来,模型参数的优化采用基于遗传算法的数据驱动方法。初步结果表明,基于遗传算法的数据驱动方法具有实现建模目的的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Towards Data-Driven Modelling of Sumoylation Following Heat Shock
Understanding how cell fate is determined when exposed to extreme stresses such as heat shock is critical in biomedical systems. It has long been understood that exposure of cells to high temperature typically protect themselves with a heat shock response (HSR), where accumulation of denatured or unfolded proteins triggers the synthesis of heat shock proteins (HSPs) through the heat shock transcription factor, e.g., heat shock factor 1 (HSF1). Recent experimental work has also shown that protein posttranslational modifications (PTMs) such as SUMOylation play crucial roles in cellular responses to heat shock. As a complementary approach to the current experimental methodologies, in this study we aim to develop a mathematical model of SUMOylation-development synergism of HSR for the purpose of studying the dynamical behaviour of HSR quantitatively. The structure of our dynamical model is derived mostly from mass action kinetics while the model parameters are optimized by using a genetic algorithm (GA) based data-driven approach. The preliminary results show GA based data-driven approach has potentials for our modelling purpose.
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