Team:Bologna/Modeling

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(Mathematical Model)
(Mathematical Model)
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[[Image:Circuito2.jpg|700px|center]]
[[Image:Circuito2.jpg|700px|center]]
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The behavior of this device and the conditions for bistability can be understood using the following differential equations for the network:
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The genetic circuit in Figure 1 can be modeled with the following equations:
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Revision as of 09:14, 16 October 2008

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Mathematical Model


Circuito2.jpg

The genetic circuit in Figure 1 can be modeled with the following equations:


Equazione0.jpg


Where:
α = promoter activity and rbs
δ = coefficient of degradation (cellular diluition)
μ = coefficient of cooperativity


Equazione3.jpg







Equazione4.jpg






Equazione5.jpg






Equazione6.jpg






Equazione7.jpg






Equazione8.jpg






Equazione9.jpg






Equazione10.jpg













The circuit in Figure 1 can be modeled with the following equations:

Eq1.jpg

Where:

Tab.jpg
In the model we distinguish between protein binded to repressor (
F01.jpg
)and protein free, not binded to repressor (
F02.jpg
), in this case repressor is represented by IPTG. Knowing that and the law of mass action
F2a.jpg
is possible write
F3.jpg
where we can replace
F4.jpg
represents the entry of IPTG inside the cell. The same thing can be done even for LexA obtaining
F5.jpg
where
F6.jpg
represents the UV radiation.

Placing:

F7.jpg

The dimensionless equations are:

F8.jpg

Hypothesizing: to be under conditions of equilibrium;

all the entries are void (); the affinity of the repressor for the operator site is high, for as we have been defined it will surely be smaller of one so ;

the cooperativity is the same both for the LacI and for TetR and it is worth 2; the equations become:

Bibliography

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