The stochastic behavior of a molecular switching circuit with feedback

<p>Abstract</p> <p>Background</p> <p>Using a statistical physics approach, we study the stochastic switching behavior of a model circuit of multisite phosphorylation and dephosphorylation with feedback. The circuit consists of a kinase and phosphatase acting on multiple...

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Main Authors: Smith Eric, Krishnamurthy Supriya, Krakauer David, Fontana Walter
Format: Article
Language:English
Published: BMC 2007-05-01
Series:Biology Direct
Online Access:http://www.biology-direct.com/content/2/1/13
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spelling doaj-1550c63701114080bdb0adf8410ae9c42020-11-25T00:23:17ZengBMCBiology Direct1745-61502007-05-01211310.1186/1745-6150-2-13The stochastic behavior of a molecular switching circuit with feedbackSmith EricKrishnamurthy SupriyaKrakauer DavidFontana Walter<p>Abstract</p> <p>Background</p> <p>Using a statistical physics approach, we study the stochastic switching behavior of a model circuit of multisite phosphorylation and dephosphorylation with feedback. The circuit consists of a kinase and phosphatase acting on multiple sites of a substrate that, contingent on its modification state, catalyzes its own phosphorylation and, in a symmetric scenario, dephosphorylation. The symmetric case is viewed as a cartoon of conflicting feedback that could result from antagonistic pathways impinging on the state of a shared component.</p> <p>Results</p> <p>Multisite phosphorylation is sufficient for bistable behavior under feedback even when catalysis is linear in substrate concentration, which is the case we consider. We compute the phase diagram, fluctuation spectrum and large-deviation properties related to switch memory within a statistical mechanics framework. Bistability occurs as either a first-order or second-order non-equilibrium phase transition, depending on the network symmetries and the ratio of phosphatase to kinase numbers. In the second-order case, the circuit never leaves the bistable regime upon increasing the number of substrate molecules at constant kinase to phosphatase ratio.</p> <p>Conclusion</p> <p>The number of substrate molecules is a key parameter controlling both the onset of the bistable regime, fluctuation intensity, and the residence time in a switched state. The relevance of the concept of memory depends on the degree of switch symmetry, as memory presupposes information to be remembered, which is highest for equal residence times in the switched states.</p> <p>Reviewers</p> <p>This article was reviewed by Artem Novozhilov (nominated by Eugene Koonin), Sergei Maslov, and Ned Wingreen.</p> http://www.biology-direct.com/content/2/1/13
collection DOAJ
language English
format Article
sources DOAJ
author Smith Eric
Krishnamurthy Supriya
Krakauer David
Fontana Walter
spellingShingle Smith Eric
Krishnamurthy Supriya
Krakauer David
Fontana Walter
The stochastic behavior of a molecular switching circuit with feedback
Biology Direct
author_facet Smith Eric
Krishnamurthy Supriya
Krakauer David
Fontana Walter
author_sort Smith Eric
title The stochastic behavior of a molecular switching circuit with feedback
title_short The stochastic behavior of a molecular switching circuit with feedback
title_full The stochastic behavior of a molecular switching circuit with feedback
title_fullStr The stochastic behavior of a molecular switching circuit with feedback
title_full_unstemmed The stochastic behavior of a molecular switching circuit with feedback
title_sort stochastic behavior of a molecular switching circuit with feedback
publisher BMC
series Biology Direct
issn 1745-6150
publishDate 2007-05-01
description <p>Abstract</p> <p>Background</p> <p>Using a statistical physics approach, we study the stochastic switching behavior of a model circuit of multisite phosphorylation and dephosphorylation with feedback. The circuit consists of a kinase and phosphatase acting on multiple sites of a substrate that, contingent on its modification state, catalyzes its own phosphorylation and, in a symmetric scenario, dephosphorylation. The symmetric case is viewed as a cartoon of conflicting feedback that could result from antagonistic pathways impinging on the state of a shared component.</p> <p>Results</p> <p>Multisite phosphorylation is sufficient for bistable behavior under feedback even when catalysis is linear in substrate concentration, which is the case we consider. We compute the phase diagram, fluctuation spectrum and large-deviation properties related to switch memory within a statistical mechanics framework. Bistability occurs as either a first-order or second-order non-equilibrium phase transition, depending on the network symmetries and the ratio of phosphatase to kinase numbers. In the second-order case, the circuit never leaves the bistable regime upon increasing the number of substrate molecules at constant kinase to phosphatase ratio.</p> <p>Conclusion</p> <p>The number of substrate molecules is a key parameter controlling both the onset of the bistable regime, fluctuation intensity, and the residence time in a switched state. The relevance of the concept of memory depends on the degree of switch symmetry, as memory presupposes information to be remembered, which is highest for equal residence times in the switched states.</p> <p>Reviewers</p> <p>This article was reviewed by Artem Novozhilov (nominated by Eugene Koonin), Sergei Maslov, and Ned Wingreen.</p>
url http://www.biology-direct.com/content/2/1/13
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