共 2 条
Integrating tracer-based metabolomics data and metabolic fluxes in a linear fashion via Elementary Carbon Modes
被引:8
|作者:
Pey, Jon
[2
,3
]
Rubio, Angel
[2
,3
]
Theodoropoulos, Constantinos
[4
]
Cascante, Marta
[1
]
Planes, Francisco J.
[2
,3
]
机构:
[1] Univ Barcelona, Fac Biol, Inst Biomed IBUB, Unit CSIC, E-08028 Barcelona, Spain
[2] Univ Navarra, CEIT, San Sebastian 20018, Spain
[3] Univ Navarra, TECNUN, San Sebastian 20018, Spain
[4] Univ Manchester, Sch Chem Engn & Analyt Sci, Manchester M13 9PL, Lancs, England
关键词:
Metabolic Flux Analysis;
Isotope Labeling Experiments;
Constraints-based modeling;
Elementary Carbon Modes;
Flux Variability Analysis;
ISOTOPOMER DISTRIBUTIONS;
ESCHERICHIA-COLI;
SYSTEMS BIOLOGY;
SCALE MODELS;
NETWORKS;
RECONSTRUCTION;
ALGORITHM;
CELLS;
UNITS;
D O I:
10.1016/j.ymben.2012.03.011
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
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. (C) 2012 Elsevier Inc. All rights reserved.
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页码:344 / 353
页数:10
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