Team:NTNU Trondheim/Yeast

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(Overview)
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==Overview==
==Overview==
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Our part of the collaboration with RHiT was helping them with stochastic modelling of the trigger system for mating in yeast. The full mechanism has been quite well studied, but it is very complicated[http://dx.doi.org/10.1002/yea.1122]. In RHiTs [[Team:RHIT/Modeling|model]], the final steps of the mechanism is activation of the Ste12 protein by Fus3.
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Our part of the collaboration with RHiT was helping them with stochastic modelling of the trigger system for mating in yeast. The full mechanism has been quite well studied, but it is very complicated[http://dx.doi.org/10.1002/yea.1122]. In RHiTs [[Team:RHIT/Modeling|model]], the final steps of the mechanism is activation of the Ste12 protein by Fus3. To simplify the model, production of Fus3 in the model was described by a sigmoid curvefound in experiments[http://dx.doi.org/10.1038/nature08946].

Revision as of 11:04, 14 August 2012

NTNU IS B.A.C.K.
Bacterial Anti-Cancer-Kamikaze

Collaboration with RHiT; Yeast modelling

Contents


Overview

Our part of the collaboration with RHiT was helping them with stochastic modelling of the trigger system for mating in yeast. The full mechanism has been quite well studied, but it is very complicated[1]. In RHiTs model, the final steps of the mechanism is activation of the Ste12 protein by Fus3. To simplify the model, production of Fus3 in the model was described by a sigmoid curvefound in experiments[2].

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