• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

通量平衡分析:几何学视角

Flux balance analysis: a geometric perspective.

作者信息

Smallbone Kieran, Simeonidis Evangelos

机构信息

Manchester Centre for Integrative Systems Biology, Manchester Interdisciplinary Biocentre, 131 Princess Street, Manchester M1 7DN, UK.

出版信息

J Theor Biol. 2009 May 21;258(2):311-5. doi: 10.1016/j.jtbi.2009.01.027. Epub 2009 Feb 7.

DOI:10.1016/j.jtbi.2009.01.027
PMID:19490860
Abstract

Advances in the field of bioinformatics have led to reconstruction of genome-scale networks for a number of key organisms. The application of physicochemical constraints to these stoichiometric networks allows researchers, through methods such as flux balance analysis, to highlight key sets of reactions necessary to achieve particular objectives. The key benefits of constraint-based analysis lie in the minimal knowledge required to infer systemic properties. However, network degeneracy leads to a large number of flux distributions that satisfy any objective; moreover, these distributions may be dominated by biologically irrelevant internal cycles. By examining the geometry underlying the problem, we define two methods for finding a unique solution within the space of all possible flux distributions; such a solution contains no internal cycles, and is representative of the space as a whole. The first method draws on typical geometric knowledge, but cannot be applied to large networks because of the high computational complexity of the problem. Thus a second method, an iteration of linear programs which scales easily to the genome scale, is defined. The algorithm is run on four recent genome-scale models, and unique flux solutions are found. The algorithm set out here will allow researchers in flux balance analysis to exchange typical solutions to their models in a reproducible format. Moreover, having found a single solution, statistical analyses such as correlations may be performed.

摘要

生物信息学领域的进展已促使人们为许多关键生物体重建了基因组规模的网络。将物理化学约束应用于这些化学计量网络,使研究人员能够通过通量平衡分析等方法,突出实现特定目标所需的关键反应集。基于约束分析的主要优势在于推断系统特性所需的知识最少。然而,网络简并会导致大量满足任何目标的通量分布;此外,这些分布可能由生物学上无关的内部循环主导。通过研究该问题背后的几何结构,我们定义了两种在所有可能的通量分布空间内找到唯一解的方法;这样的解不包含内部循环,并且代表了整个空间。第一种方法借鉴了典型的几何知识,但由于问题的计算复杂度高,无法应用于大型网络。因此,定义了第二种方法,即一种易于扩展到基因组规模的线性规划迭代方法。该算法在四个最新的基因组规模模型上运行,并找到了唯一的通量解。这里提出的算法将使通量平衡分析领域的研究人员能够以可重复的格式交换其模型的典型解。此外,在找到单个解后,可以进行相关性等统计分析。

相似文献

1
Flux balance analysis: a geometric perspective.通量平衡分析:几何学视角
J Theor Biol. 2009 May 21;258(2):311-5. doi: 10.1016/j.jtbi.2009.01.027. Epub 2009 Feb 7.
2
Estimating Metabolic Fluxes Using a Maximum Network Flexibility Paradigm.使用最大网络灵活性范式估算代谢通量。
PLoS One. 2015 Oct 12;10(10):e0139665. doi: 10.1371/journal.pone.0139665. eCollection 2015.
3
Accelerating flux balance calculations in genome-scale metabolic models by localizing the application of loopless constraints.通过将无环约束应用本地化来加速基因组规模代谢模型中的通量平衡计算。
Bioinformatics. 2018 Dec 15;34(24):4248-4255. doi: 10.1093/bioinformatics/bty446.
4
Capturing the essence of a metabolic network: a flux balance analysis approach.捕捉代谢网络的本质:通量平衡分析方法。
J Theor Biol. 2009 Oct 7;260(3):445-52. doi: 10.1016/j.jtbi.2009.06.013. Epub 2009 Jun 21.
5
Genome-scale model for Clostridium acetobutylicum: Part II. Development of specific proton flux states and numerically determined sub-systems.丙酮丁醇梭菌的基因组规模模型:第二部分。特定质子通量状态的发展及数值确定的子系统。
Biotechnol Bioeng. 2008 Dec 1;101(5):1053-71. doi: 10.1002/bit.22009.
6
Sampling the solution space in genome-scale metabolic networks reveals transcriptional regulation in key enzymes.对基因组规模代谢网络中的解决方案空间进行采样,揭示了关键酶的转录调控。
PLoS Comput Biol. 2010 Jul 15;6(7):e1000859. doi: 10.1371/journal.pcbi.1000859.
7
Sampling with poling-based flux balance analysis: optimal versus sub-optimal flux space analysis of Actinobacillus succinogenes.基于投票的通量平衡分析采样:琥珀酸放线杆菌的最优通量空间分析与次优通量空间分析
BMC Bioinformatics. 2015 Feb 18;16:49. doi: 10.1186/s12859-015-0476-5.
8
FCDECOMP: decomposition of metabolic networks based on flux coupling relations.FCDECOMP:基于通量耦合关系的代谢网络分解
J Bioinform Comput Biol. 2014 Oct;12(5):1450028. doi: 10.1142/S0219720014500280.
9
Characterizing the optimal flux space of genome-scale metabolic reconstructions through modified latin-hypercube sampling.通过改进的拉丁超立方抽样表征基因组规模代谢重建的最优通量空间。
Mol Biosyst. 2016 Mar;12(3):994-1005. doi: 10.1039/c5mb00457h.
10
optGpSampler: an improved tool for uniformly sampling the solution-space of genome-scale metabolic networks.optGpSampler:一种用于均匀采样基因组规模代谢网络解空间的改进工具。
PLoS One. 2014 Feb 14;9(2):e86587. doi: 10.1371/journal.pone.0086587. eCollection 2014.

引用本文的文献

1
Analyzing sorbitol biosynthesis using a metabolic network flux model of a lichenized strain of the green microalga .使用绿色微藻地衣化菌株的代谢网络通量模型分析山梨醇生物合成。
Microbiol Spectr. 2025 Jan 7;13(1):e0366023. doi: 10.1128/spectrum.03660-23. Epub 2024 Dec 9.
2
Predicting microbial interactions with approaches based on flux balance analysis: an evaluation.基于通量平衡分析的微生物相互作用预测方法评估。
BMC Bioinformatics. 2024 Jan 23;25(1):36. doi: 10.1186/s12859-024-05651-7.
3
Applications of genome-scale metabolic models to investigate microbial metabolic adaptations in response to genetic or environmental perturbations.
应用基因组规模代谢模型研究微生物代谢适应遗传或环境扰动的反应。
Brief Bioinform. 2023 Nov 22;25(1). doi: 10.1093/bib/bbad439.
4
Characterizing cancer metabolism from bulk and single-cell RNA-seq data using METAFlux.使用 METAFlux 从批量和单细胞 RNA-seq 数据中描绘癌症代谢。
Nat Commun. 2023 Aug 12;14(1):4883. doi: 10.1038/s41467-023-40457-w.
5
Constraint-Based Reconstruction and Analyses of Metabolic Models: Open-Source Python Tools and Applications to Cancer.基于约束的代谢模型重建与分析:用于癌症研究的开源Python工具及应用
Front Oncol. 2022 Jul 7;12:914594. doi: 10.3389/fonc.2022.914594. eCollection 2022.
6
Modeling energy depletion in rat livers using Nash equilibrium metabolic pathway analysis.利用纳什均衡代谢途径分析对大鼠肝脏能量耗竭进行建模。
Sci Rep. 2022 Mar 3;12(1):3496. doi: 10.1038/s41598-022-06966-2.
7
Rapid intensification of an established CHO cell fed-batch process.已建立的 CHO 细胞补料分批培养过程的快速强化。
Biotechnol Prog. 2022 Jan;38(1):e3213. doi: 10.1002/btpr.3213. Epub 2021 Sep 25.
8
Metabolic flux configuration determination using information entropy.基于信息熵的代谢通量分布测定
PLoS One. 2020 Dec 4;15(12):e0243067. doi: 10.1371/journal.pone.0243067. eCollection 2020.
9
A Distance-Based Framework for the Characterization of Metabolic Heterogeneity in Large Sets of Genome-Scale Metabolic Models.一种基于距离的框架,用于刻画大量基因组规模代谢模型中的代谢异质性
Patterns (N Y). 2020 Aug 6;1(6):100080. doi: 10.1016/j.patter.2020.100080. eCollection 2020 Sep 11.
10
Human Systems Biology and Metabolic Modelling: A Review-From Disease Metabolism to Precision Medicine.人类系统生物学与代谢建模:综述——从疾病代谢到精准医学。
Biomed Res Int. 2019 Jun 9;2019:8304260. doi: 10.1155/2019/8304260. eCollection 2019.