Literature DB >> 2520172

Use of implicit methods from general sensitivity theory to develop a systematic approach to metabolic control. II. Complex systems.

M Cascante, R Franco, E I Canela.   

Abstract

In the accompanying paper (Cascante et al., this issue) we have used general sensitivity theory to develop a matrix algebra that, in the case of sequential reactions, directly relates global and local properties of a given system. In complex biochemical systems this direct relationship is not possible due to the existence of linear dependencies among fluxes and among metabolite concentrations (conserved aggregate concentrations in BST or moiety-conserved concentrations in MCT). In this paper our matrix algebra is applied to conserved cycles and branched pathways, and it is shown that with minor modifications it again relates global properties to the local properties of the enzymes in the system. In the case of conserved cycles, elasticities become modified due to the existence of linear dependencies among the concentration variables in the cycle. In branched pathways, new matrix elements involving ratios of fluxes appear. With these modifications, one can show that the so-called theorems of metabolic control theory specific to these types of pathways are special cases of more general relationships. Rules for the construction of matrices relating global and local properties are given that apply to an arbitrary system of cycles and branches. The implicit approach developed in these papers, which is a generalization of that used in MCT, allows one to make more direct comparisons with the general explicit approach originally developed in BST.

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Year:  1989        PMID: 2520172     DOI: 10.1016/0025-5564(89)90068-0

Source DB:  PubMed          Journal:  Math Biosci        ISSN: 0025-5564            Impact factor:   2.144


  16 in total

1.  Product dependence and bifunctionality compromise the ultrasensitivity of signal transduction cascades.

Authors:  Fernando Ortega; Luis Acerenza; Hans V Westerhoff; Francesc Mas; Marta Cascante
Journal:  Proc Natl Acad Sci U S A       Date:  2002-02-05       Impact factor: 11.205

2.  Elasticity analysis and design for large metabolic responses produced by changes in enzyme activities.

Authors:  Fernando Ortega; Luis Acerenza
Journal:  Biochem J       Date:  2002-10-01       Impact factor: 3.857

Review 3.  Metabolic control analysis: a survey of its theoretical and experimental development.

Authors:  D A Fell
Journal:  Biochem J       Date:  1992-09-01       Impact factor: 3.857

4.  Quantitative analysis of metabolic regulation. A graph-theoretic approach using spanning trees.

Authors:  A K Sen
Journal:  Biochem J       Date:  1991-04-01       Impact factor: 3.857

5.  Control analysis of transition times. Extension of analysis and matrix method.

Authors:  M Cascante; N V Torres; R Franco; E Meléndez-Hevia; E I Canela
Journal:  Mol Cell Biochem       Date:  1991-02-27       Impact factor: 3.396

6.  Calculation of control coefficients of metabolic pathways. A flux-oriented graph-theoretic approach.

Authors:  A K Sen
Journal:  Biochem J       Date:  1991-10-01       Impact factor: 3.857

7.  Algorithms for the derivation of Flux and Concentration Control Coefficients.

Authors:  A R Schulz
Journal:  Biochem J       Date:  1991-08-15       Impact factor: 3.857

8.  Control theory of metabolic channelling.

Authors:  B N Kholodenko; M Cascante; H V Westerhoff
Journal:  Mol Cell Biochem       Date:  1995-02-23       Impact factor: 3.396

9.  Preclinical models for interrogating drug action in human cancers using Stable Isotope Resolved Metabolomics (SIRM).

Authors:  Andrew N Lane; Richard M Higashi; Teresa W-M Fan
Journal:  Metabolomics       Date:  2016-06-29       Impact factor: 4.290

10.  Validation and steady-state analysis of a power-law model of purine metabolism in man.

Authors:  R Curto; E O Voit; A Sorribas; M Cascante
Journal:  Biochem J       Date:  1997-06-15       Impact factor: 3.857

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