Email updates

Keep up to date with the latest news and content from BMC Systems Biology and BioMed Central.

Open Access Research article

The logic of kinetic regulation in the thioredoxin system

Ché S Pillay1*, Jan-Hendrik S Hofmeyr23 and Johann M Rohwer2

Author Affiliations

1 Discipline of Genetics, University of KwaZulu-Natal, South Africa, Carbis Road, Pietermaritzburg, 3201, South Africa

2 Triple-J Group for Molecular Cell Physiology, Department of Biochemistry, Stellenbosch University, Van der Byl Street, Stellenbosch 7600, South Africa

3 Centre for Studies in Complexity, Stellenbosch University, Marais Street, Stellenbosch, 7600, South Africa

For all author emails, please log on.

BMC Systems Biology 2011, 5:15  doi:10.1186/1752-0509-5-15

Published: 25 January 2011

Abstract

Background

The thioredoxin system consisting of NADP(H), thioredoxin reductase and thioredoxin provides reducing equivalents to a large and diverse array of cellular processes. Despite a great deal of information on the kinetics of individual thioredoxin-dependent reactions, the kinetic regulation of this system as an integrated whole is not known. We address this by using kinetic modeling to identify and describe kinetic behavioral motifs found within the system.

Results

Analysis of a realistic computational model of the Escherichia coli thioredoxin system revealed several modes of kinetic regulation in the system. In keeping with published findings, the model showed that thioredoxin-dependent reactions were adaptable (i.e. changes to the thioredoxin system affected the kinetic profiles of these reactions). Further and in contrast to other systems-level descriptions, analysis of the model showed that apparently unrelated thioredoxin oxidation reactions can affect each other via their combined effects on the thioredoxin redox cycle. However, the scale of these effects depended on the kinetics of the individual thioredoxin oxidation reactions with some reactions more sensitive to changes in the thioredoxin cycle and others, such as the Tpx-dependent reduction of hydrogen peroxide, less sensitive to these changes. The coupling of the thioredoxin and Tpx redox cycles also allowed for ultrasensitive changes in the thioredoxin concentration in response to changes in the thioredoxin reductase concentration. We were able to describe the kinetic mechanisms underlying these behaviors precisely with analytical solutions and core models.

Conclusions

Using kinetic modeling we have revealed the logic that underlies the functional organization and kinetic behavior of the thioredoxin system. The thioredoxin redox cycle and associated reactions allows for a system that is adaptable, interconnected and able to display differential sensitivities to changes in this redox cycle. This work provides a theoretical, systems-biological basis for an experimental analysis of the thioredoxin system and its associated reactions.