Literature DB >> 11311143

Occurrence of paradoxical or sustained control by an enzyme when overexpressed: necessary conditions and experimental evidence with regard to hepatic glucokinase.

P De Atauri1, L Acerenza, B N Kholodenko, N De La Iglesia, J J Guinovart, L Agius, M Cascante.   

Abstract

It is widely assumed that the control coefficient of an enzyme on pathway flux decreases as the concentration of enzyme increases. However, it has been shown [Kholodenko and Brown (1996) Biochem. J. 314, 753-760] that enzymes with sigmoidal kinetics can maintain or even gain control with an increase in enzyme activity or concentration. This has been described as 'paradoxical control'. Here we formulate the general requirements for allosteric enzyme kinetics to display this behaviour. We show that a necessary condition is that the Hill coefficient of the enzyme should increase with an increase in substrate concentration or decrease with an increase in product concentration. We also describe the necessary and sufficient requirements for the occurrence of paradoxical control in terms of the flux control coefficients and the derivatives of the elasticities. The derived expression shows that the higher the control coefficient of an allosteric enzyme, the more likely it is that the pathway will display this behaviour. Control of pathway flux is generally shared between a large number of enzymes and therefore the likelihood of observing sustained or increased control is low, even if the kinetic parameters are in the most favourable range to generate the phenomenon. We show that hepatic glucokinase, which has a very high flux control coefficient and displays sigmoidal behaviour within the hepatocyte in situ as a result of interaction with a regulatory protein, displays sustained or increased control over an extended range of enzyme concentrations when the regulatory protein is overexpressed.

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Year:  2001        PMID: 11311143      PMCID: PMC1221796          DOI: 10.1042/bj3550787

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  17 in total

1.  Increasing the flux in metabolic pathways: A metabolic control analysis perspective

Authors: 
Journal:  Biotechnol Bioeng       Date:  1998-04-05       Impact factor: 4.530

2.  ON THE NATURE OF ALLOSTERIC TRANSITIONS: A PLAUSIBLE MODEL.

Authors:  J MONOD; J WYMAN; J P CHANGEUX
Journal:  J Mol Biol       Date:  1965-05       Impact factor: 5.469

3.  Metabolic control analysis. Sensitivity of control coefficients to elasticities.

Authors:  J R Small; D A Fell
Journal:  Eur J Biochem       Date:  1990-07-31

4.  The physiological role of glucokinase binding and translocation in hepatocytes.

Authors:  L Agius
Journal:  Adv Enzyme Regul       Date:  1998

5.  A linear steady-state treatment of enzymatic chains. General properties, control and effector strength.

Authors:  R Heinrich; T A Rapoport
Journal:  Eur J Biochem       Date:  1974-02-15

6.  Responses of metabolic systems to large changes in enzyme activities and effectors. 1. The linear treatment of unbranched chains.

Authors:  J R Small; H Kacser
Journal:  Eur J Biochem       Date:  1993-04-01

7.  Responses of metabolic systems to large changes in enzyme activities and effectors. 2. The linear treatment of branched pathways and metabolite concentrations. Assessment of the general non-linear case.

Authors:  J R Small; H Kacser
Journal:  Eur J Biochem       Date:  1993-04-01

8.  Investigation of the mechanism by which glucose analogues cause translocation of glucokinase in hepatocytes: evidence for two glucose binding sites.

Authors:  L Agius; M Stubbs
Journal:  Biochem J       Date:  2000-03-01       Impact factor: 3.857

9.  Evidence for a role of glucose-induced translocation of glucokinase in the control of hepatic glycogen synthesis.

Authors:  L Agius; M Peak; C B Newgard; A M Gomez-Foix; J J Guinovart
Journal:  J Biol Chem       Date:  1996-11-29       Impact factor: 5.157

Review 10.  Short-term control of glucokinase activity: role of a regulatory protein.

Authors:  E Van Schaftingen; M Detheux; M Veiga da Cunha
Journal:  FASEB J       Date:  1994-04-01       Impact factor: 5.191

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  2 in total

1.  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

2.  Metabolic control analysis aimed at the ribose synthesis pathways of tumor cells: a new strategy for antitumor drug development.

Authors:  Joan Boren; Antonio Ramos Montoya; Pedro de Atauri; Begoña Comin-Anduix; Antonio Cortes; Josep J Centelles; Wilma M Frederiks; Cornelis J F Van Noorden; Marta Cascante
Journal:  Mol Biol Rep       Date:  2002       Impact factor: 2.316

  2 in total

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