From flux analysis to self contained cellular models.

IF 2.3
Frontiers in systems biology Pub Date : 2025-08-22 eCollection Date: 2025-01-01 DOI:10.3389/fsysb.2025.1546072
Andreas Kremling
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Abstract

Mathematical models for cellular systems have become more and more important for understanding the complex interplay between metabolism, signalling, and gene expression.In this manuscript, starting from the well-known flux balance analysis, tools and methods are summarised and illustrated by various examples that describe the way to models with kinetics for individual reactions steps that are finally self-contained. While flux analysis requires known (measured) input fluxes, self-contained (or self-sustained) models only get information on concentrations of environmental components. Kinetic reaction laws, feedback structures, and protein allocation then determine the temporal output of all intracellular metabolites and macromolecules. Emphasis is placed on (i) mass conservation, a crucial system property frequently overlooked in models incorporating cellular structures like macromolecular structures like proteins, RNA, and DNA, and (ii) thermodynamic constraints which further limit the solution space. Matlab Live Scripts are provided for all simulation studies shown and additional reading material is given in the appendix.

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从通量分析到自包含细胞模型。
细胞系统的数学模型对于理解代谢、信号传导和基因表达之间复杂的相互作用变得越来越重要。在这份手稿中,从众所周知的通量平衡分析开始,工具和方法被总结和说明了各种例子,这些例子描述了个体反应步骤的动力学模型,最终是自包含的。通量分析需要已知的(测量的)输入通量,而自给自足的(或自我维持的)模型只能得到有关环境成分浓度的信息。动力学反应规律、反馈结构和蛋白质分配决定了所有细胞内代谢物和大分子的时间输出。重点放在(i)质量守恒,这是一个重要的系统特性,在包含细胞结构(如蛋白质、RNA和DNA等大分子结构)的模型中经常被忽视,以及(ii)进一步限制溶液空间的热力学约束。本文为所有模拟研究提供了Matlab实时脚本,附录中提供了额外的阅读材料。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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