A domain-oriented approach to the reduction of combinatorial complexity in signal transduction networksReport as inadecuate




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BMC Bioinformatics

, 7:34

First Online: 23 January 2006Received: 16 April 2005Accepted: 23 January 2006

Abstract

Background:Receptors and scaffold proteins possess a number of distinct domains and bind multiple partners. A common problem in modeling signaling systems arises from a combinatorial explosion of different states generated by feasible molecular species. The number of possible species grows exponentially with the number of different docking sites and can easily reach several millions. Models accounting for this combinatorial variety become impractical for many applications.

Results:Our results show that under realistic assumptions on domain interactions, the dynamics of signaling pathways can be exactly described by reduced, hierarchically structured models. The method presented here provides a rigorous way to model a large class of signaling networks using macro-states macroscopic quantities such as the levels of occupancy of the binding domains instead of micro-states concentrations of individual species. The method is described using generic multidomain proteins and is applied to the molecule LAT.

Conclusion:The presented method is a systematic and powerful tool to derive reduced model structures describing the dynamics of multiprotein complex formation accurately.

Electronic supplementary materialThe online version of this article doi:10.1186-1471-2105-7-34 contains supplementary material, which is available to authorized users.

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Author: Holger Conzelmann - Julio Saez-Rodriguez - Thomas Sauter - Boris N Kholodenko - Ernst D Gilles

Source: https://link.springer.com/







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