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使用k-模块对代谢网络进行层次分解。

Hierarchical decomposition of metabolic networks using k-modules.

作者信息

Reimers Arne C

机构信息

Centre for Mathematics and Computer Science (CWI), Science Park 123, 1098 XG Amsterdam, The Netherlands

出版信息

Biochem Soc Trans. 2015 Dec;43(6):1146-50. doi: 10.1042/BST20150143.

Abstract

The optimal solutions obtained by flux balance analysis (FBA) are typically not unique. Flux modules have recently been shown to be a very useful tool to simplify and decompose the space of FBA-optimal solutions. Since yield-maximization is sometimes not the primary objective encountered in vivo, we are also interested in understanding the space of sub-optimal solutions. Unfortunately, the flux modules are too restrictive and not suited for this task. We present a generalization, called k-module, which compensates the limited applicability of flux modules to the space of sub-optimal solutions. Intuitively, a k-module is a sub-network with low connectivity to the rest of the network. Recursive application of k-modules yields a hierarchical decomposition of the metabolic network, which is also known as branch decomposition in matroid theory. In particular, decompositions computed by existing methods, like the null-space-based approach, introduced by Poolman et al. [(2007) J. Theor. Biol. 249: , 691-705] can be interpreted as branch decompositions. With k-modules we can now compare alternative decompositions of metabolic networks to the classical sub-systems of glycolysis, tricarboxylic acid (TCA) cycle, etc. They can be used to speed up algorithmic problems [theoretically shown for elementary flux modes (EFM) enumeration] and have the potential to present computational solutions in a more intuitive way independently from the classical sub-systems.

摘要

通量平衡分析(FBA)得到的最优解通常并非唯一。通量模块最近被证明是一种非常有用的工具,可用于简化和分解FBA最优解的空间。由于产量最大化有时并非体内所遇到的主要目标,因此我们也有兴趣了解次优解的空间。不幸的是,通量模块限制过多,不适用于此任务。我们提出了一种推广,称为k模块,它弥补了通量模块在次优解空间中适用性有限的问题。直观地说,k模块是一个与网络其余部分连接性较低的子网。k模块的递归应用会产生代谢网络的层次分解,这在拟阵理论中也称为分支分解。特别是,现有方法(如Poolman等人[(2007) J. Theor. Biol. 249: 691 - 705]引入的基于零空间的方法)计算出的分解可以解释为分支分解。借助k模块,我们现在可以将代谢网络的替代分解与糖酵解、三羧酸(TCA)循环等经典子系统进行比较。它们可用于加速算法问题(理论上已针对基本通量模式(EFM)枚举进行了证明),并且有可能以一种更直观的方式呈现计算解决方案,而无需依赖经典子系统。

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