Modelling

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===Mathematical Modelling===
===Mathematical Modelling===
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To create a predictive model, we used a set of differential equations to graph the approximate concentrations of each chemical with respect to time. These graphs are intended to illustrate the relative concentrations of the chemicals involved for each possible combination of input A and input B, red light and tetracycline respectively.  
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To create a predictive model, we used ordinary differential equations (ODEs) to characterize the concentrations of each protein with respect to time. The form of the ODEs is as below:
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[[Image:UW_equation.jpg|300px|center]]
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with basal expression of a protein, Hill function describing gene regulation and protein decay (Szallasi et. al, 2006).
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Scenario 1 of the graph illustrates the concentration of chemicals when adding 0+0, showing no production of either GFP or RFP. Scenario 2 illustrates the 0+1 case, showing production of GFP; similarly, scenario 3 illustrates the 1+0 case, also resulting in GFP. Finally scenario 4 illustrates 1+1 case where both inputs being on results in production of RFP.
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The following graphs are the simulation results, showing the relative concentrations of proteins involved for each possible combination of input A and input B, red light and tetracycline respectively. Scenario 1 of the graph illustrates the concentration of chemicals when adding 0+0, showing no production of either GFP or RFP. Scenario 2 illustrates the 0+1 case, showing production of GFP; similarly, scenario 3 illustrates the 1+0 case, also resulting in GFP. Finally scenario 4 illustrates 1+1 case where both inputs being on results in production of RFP.
   
   
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[[Image:UW_equation.jpg|300px|center]]<br>
 
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[[Image:UW_Graphs.png|thumb|center|800px|Mathematical modelling of the bacterial half-adder]]
 
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[[Image:UW_Graphs.png|thumb|center|800px|Simulation results of the bacterial half-adder]]
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Z. Szallasi, V. Periwal, J. Stelling (eds), ''System Modeling in Cellular Biology: From Concepts to Nuts and Bolts'', MIT Press, Cambridge, MA, 125-148, 2006.
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   [[Waterloo | Home ]] | [[Project | Project]] | [[Modelling | Mathematical Modelling]] | [[Construction_&_Testing | Construction & Testing]] | [[Future_Work | Future Work]]  
   [[Waterloo | Home ]] | [[Project | Project]] | [[Modelling | Mathematical Modelling]] | [[Construction_&_Testing | Construction & Testing]] | [[Future_Work | Future Work]]  
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Revision as of 20:43, 26 October 2007

Mathematical Modelling

To create a predictive model, we used ordinary differential equations (ODEs) to characterize the concentrations of each protein with respect to time. The form of the ODEs is as below:

UW equation.jpg

with basal expression of a protein, Hill function describing gene regulation and protein decay (Szallasi et. al, 2006).

The following graphs are the simulation results, showing the relative concentrations of proteins involved for each possible combination of input A and input B, red light and tetracycline respectively. Scenario 1 of the graph illustrates the concentration of chemicals when adding 0+0, showing no production of either GFP or RFP. Scenario 2 illustrates the 0+1 case, showing production of GFP; similarly, scenario 3 illustrates the 1+0 case, also resulting in GFP. Finally scenario 4 illustrates 1+1 case where both inputs being on results in production of RFP.


Simulation results of the bacterial half-adder


Z. Szallasi, V. Periwal, J. Stelling (eds), System Modeling in Cellular Biology: From Concepts to Nuts and Bolts, MIT Press, Cambridge, MA, 125-148, 2006.

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