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Originally published as Biophys J. BioFAST on November 30, 2007.
doi:10.1529/biophysj.107.115022
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Biophysical Journal 94:1995-2006 (2008)
© 2008 The Biophysical Society

Src Family Kinases and Receptors: Analysis of Three Activation Mechanisms by Dynamic Systems Modeling

Hendrik Fuß, Werner Dubitzky, C. Stephen Downes and Mary Jo Kurth

School of Biomedical Sciences, University of Ulster, Coleraine, Ireland

Correspondence: Address reprint requests to H. Fuß, E-mail: h.fuss{at}ulster.ac.uk.

Src family kinases (SFKs) interact with a number of cellular receptors. They participate in diverse signaling pathways and cellular functions. Most of the receptors involved in SFK signaling are characterized by similar modes of regulation. This computational study discusses a general kinetic model of SFK-receptor interaction. The analysis of the model reveals three major ways of SFK activation: release of inhibition by C-terminal Src kinase, weakening of the inhibitory intramolecular phosphotyrosine-SH2 interaction, and amplification of a stimulating kinase activity. The SFK model was then extended to simulate interaction with growth factor and T-cell receptors. The modular SFK signaling system was shown to adapt to the requirements of specific signaling contexts and yield qualitatively different responses in the different simulated environments. The model also provides a systematic overview of the major interactions between SFKs and various cellular signaling systems and identifies their common properties.







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Copyright © 2008 by the Biophysical Society.