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通过基本碳模式以线性方式整合示踪剂代谢组学数据和代谢通量。

Integrating tracer-based metabolomics data and metabolic fluxes in a linear fashion via Elementary Carbon Modes.

机构信息

CEIT and TECNUN, University of Navarra, Manuel de Lardizabal 15, 20018 San Sebastian, Spain.

出版信息

Metab Eng. 2012 Jul;14(4):344-53. doi: 10.1016/j.ymben.2012.03.011. Epub 2012 Apr 2.

Abstract

Constraints-based modeling is an emergent area in Systems Biology that includes an increasing set of methods for the analysis of metabolic networks. In order to refine its predictions, the development of novel methods integrating high-throughput experimental data is currently a key challenge in the field. In this paper, we present a novel set of constraints that integrate tracer-based metabolomics data from Isotope Labeling Experiments and metabolic fluxes in a linear fashion. These constraints are based on Elementary Carbon Modes (ECMs), a recently developed concept that generalizes Elementary Flux Modes at the carbon level. To illustrate the effect of our ECMs-based constraints, a Flux Variability Analysis approach was applied to a previously published metabolic network involving the main pathways in the metabolism of glucose. The addition of our ECMs-based constraints substantially reduced the under-determination resulting from a standard application of Flux Variability Analysis, which shows a clear progress over the state of the art. In addition, our approach is adjusted to deal with combinatorial explosion of ECMs in genome-scale metabolic networks. This extension was applied to infer the maximum biosynthetic capacity of non-essential amino acids in human metabolism. Finally, as linearity is the hallmark of our approach, its importance is discussed at a methodological, computational and theoretical level and illustrated with a practical application in the field of Isotope Labeling Experiments.

摘要

基于约束的建模是系统生物学中的一个新兴领域,它包含了越来越多的用于分析代谢网络的方法。为了改进其预测,目前该领域的一个关键挑战是开发新的方法,将高通量实验数据整合进来。在本文中,我们提出了一组新的约束条件,以线性方式整合示踪代谢组学数据和代谢通量。这些约束条件基于最近开发的概念——基本碳模式(Elementary Carbon Modes,ECMs),它在碳水平上对基本通量模式进行了推广。为了说明我们基于 ECM 的约束条件的效果,我们应用通量可变性分析方法对涉及葡萄糖代谢主要途径的先前发表的代谢网络进行了分析。与通量可变性分析的标准应用相比,我们基于 ECM 的约束条件的添加大大减少了欠定问题,这表明我们的方法比现有技术有了明显的进步。此外,我们的方法还进行了扩展,以处理基因组规模代谢网络中 ECM 的组合爆炸问题。该扩展应用于推断人类代谢中非必需氨基酸的最大生物合成能力。最后,由于线性是我们方法的特点,因此从方法学、计算和理论层面讨论了其重要性,并通过在示踪实验领域的实际应用进行了说明。

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