Team:TU-Eindhoven/IntegralModel

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(Integral Model)
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=Integral Model=
=Integral Model=
{{:Team:TU-Eindhoven/Template:Lead}}
{{:Team:TU-Eindhoven/Template:Lead}}
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The last step in creating a comprehensive model of the contrast mechanism is merging all individual models. [[Team:TU-Eindhoven/ODEModel | Previously]] the model to predict the FNR concentration in a cell was described. This model will be combined with the [[Team:TU-Eindhoven/StochasticModel | decoy sites model]], which was extended to contain the [[Team:TU-Eindhoven/FNRPromotor | specific promotor]] that was used in this research. Here, the properties of the merged model will be discussed.
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The last step in creating a comprehensive model of the contrast mechanism is merging all individual models. [[Team:TU-Eindhoven/ODEModel | Previously]] the model to predict the FNR concentration in a cell was described. This model will be combined with the [[Team:TU-Eindhoven/StochasticModel | decoy sites model]], which was extended to contain the [[Team:TU-Eindhoven/FNRPromotor | specific promoter]] that was used in this research. Here, the properties of the merged model will be discussed.
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{{:Team:TU-Eindhoven/Template:LeadEnd}}
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==Results==
==Results==
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This model was implemented as both a ODE and a stochastic model, various parameters were estimated as described on the [[Team:TU-Eindhoven/FNRPromotor| FNR promotor page]]. One of the most interesting predictions that can be derived from the integral model is the influence of adding decoy sites to the DNA on the response to oxygen. {{:Team:TU-Eindhoven/Template:Figure | id=DecoySitesOxygen}} and {{:Team:TU-Eindhoven/Template:Figure | id=DecoySitesOxygenResponse}} endeavour to visualise this prediction as clearly as possible.
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This model was implemented as both a ODE and a stochastic model, various parameters were estimated as described on the [[Team:TU-Eindhoven/FNRPromotor| FNR promoter page]]. One of the most interesting predictions that can be derived from the integral model is the influence of adding decoy sites to the DNA on the response to oxygen. {{:Team:TU-Eindhoven/Template:Figure | id=DecoySitesOxygen}} and {{:Team:TU-Eindhoven/Template:Figure | id=DecoySitesOxygenResponse}} endeavor to visualize this prediction as clearly as possible.
{{:Team:TU-Eindhoven/Template:Float | position=left | size=6 }}
{{:Team:TU-Eindhoven/Template:Float | position=left | size=6 }}
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{{:Team:TU-Eindhoven/Template:FloatEnd | caption=Reaction of the expression rate to a change in oxygen concentration. | id=DecoySitesOxygenResponse }}
{{:Team:TU-Eindhoven/Template:FloatEnd | caption=Reaction of the expression rate to a change in oxygen concentration. | id=DecoySitesOxygenResponse }}
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From {{:Team:TU-Eindhoven/Template:Figure | id=DecoySitesOxygenResponse}} it can be concluded that the sharpest response is realised using no decoy sites. Looking at {{:Team:TU-Eindhoven/Template:Figure | id=DecoySitesOxygen}} it can be seen that adding decoy sites decreases the steady state expression rate, which is undesired. For a sharper response a weaker promotor would be needed in combination with stronger decoy sites, of which results are shown in {{:Team:TU-Eindhoven/Template:Figure | id=DecoySitesOxygenSharp}}.
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From {{:Team:TU-Eindhoven/Template:Figure | id=DecoySitesOxygenResponse}} it can be concluded that the sharpest response is realized using no decoy sites. Looking at {{:Team:TU-Eindhoven/Template:Figure | id=DecoySitesOxygen}} it can be seen that adding decoy sites decreases the steady state expression rate, which is undesired. For a sharper response a weaker promoter would be needed in combination with stronger decoy sites, of which results are shown in {{:Team:TU-Eindhoven/Template:Figure | id=DecoySitesOxygenSharp}}.
{{:Team:TU-Eindhoven/Template:Float | position=left | size=6 }}
{{:Team:TU-Eindhoven/Template:Float | position=left | size=6 }}
{{:Team:TU-Eindhoven/Template:Image | filename=DecoySitesOxygenSharp.png}}
{{:Team:TU-Eindhoven/Template:Image | filename=DecoySitesOxygenSharp.png}}
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{{:Team:TU-Eindhoven/Template:FloatEnd | caption=Correlation between the expression rate and the oxygen concentration for different amounts of decoy sites using a weaker promotor (colors have the same meaning as in {{:Team:TU-Eindhoven/Template:Figure | id=DecoySitesOxygen}}). | id=DecoySitesOxygen }}
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{{:Team:TU-Eindhoven/Template:FloatEnd | caption=Correlation between the expression rate and the oxygen concentration for different amounts of decoy sites using a weaker promoter (colors have the same meaning as in {{:Team:TU-Eindhoven/Template:Figure | id=DecoySitesOxygen}}). | id=DecoySitesOxygen }}
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It can be seen that the response is sharper and more switch like, but the problem is that the expression rate decreases significantly. So using the weaker promotor would not allow for generating satisfactory MRI contrast, which is the main purpose of the project. Combining these observations, adding decoy sites to the construct appears to only have negative effects and the idea should based on the modeling be dismissed. Another conclusion that can be drawn from the models is that the expression rate needs around one hour to reach its peak, so any observable changes in protein concentration will be delayed by a little more than one hour.
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It can be seen that the response is sharper and more switch like, but the problem is that the expression rate decreases significantly. So using the weaker promoter would not allow for generating satisfactory MRI contrast, which is the main purpose of the project. Combining these observations, adding decoy sites to the construct appears to only have negative effects and the idea should based on the modeling be dismissed. Another conclusion that can be drawn from the models is that the expression rate needs around one hour to reach its peak, so any observable changes in protein concentration will be delayed by a little more than one hour.
==Sensitivity Analysis==
==Sensitivity Analysis==

Revision as of 23:44, 18 October 2013

Contents

Integral Model

The last step in creating a comprehensive model of the contrast mechanism is merging all individual models. Previously the model to predict the FNR concentration in a cell was described. This model will be combined with the decoy sites model, which was extended to contain the specific promoter that was used in this research. Here, the properties of the merged model will be discussed.

Merging the Models

In order to merge the FNR model and the decoy sites model, the exact connection between the two models had to be defined. The FNR model describes the (active) FNR concentration in the bacterial cells. This active FNR species fulfills the role of transcription factor in the decoy sites model. Using this information, the models could simply be combined by merging the Active FNR species of the FNR model and the T (transcription factor) of the decoy sites model. The resulting model schematics are depicted in .

TU-Eindhoven Images IntegralModel.jpg
IntegralModelSchematics Schematic of the integral model

Results

This model was implemented as both a ODE and a stochastic model, various parameters were estimated as described on the FNR promoter page. One of the most interesting predictions that can be derived from the integral model is the influence of adding decoy sites to the DNA on the response to oxygen. and endeavor to visualize this prediction as clearly as possible.

TU-Eindhoven Images DecoySitesOxygen.png
DecoySitesOxygen Correlation between the expression rate and the oxygen concentration for different amounts of decoy sites.
TU-Eindhoven Images DecoySitesOxygenResponse.png
DecoySitesOxygenResponse Reaction of the expression rate to a change in oxygen concentration.

From it can be concluded that the sharpest response is realized using no decoy sites. Looking at it can be seen that adding decoy sites decreases the steady state expression rate, which is undesired. For a sharper response a weaker promoter would be needed in combination with stronger decoy sites, of which results are shown in .

TU-Eindhoven Images DecoySitesOxygenSharp.png
DecoySitesOxygen Correlation between the expression rate and the oxygen concentration for different amounts of decoy sites using a weaker promoter (colors have the same meaning as in ).

It can be seen that the response is sharper and more switch like, but the problem is that the expression rate decreases significantly. So using the weaker promoter would not allow for generating satisfactory MRI contrast, which is the main purpose of the project. Combining these observations, adding decoy sites to the construct appears to only have negative effects and the idea should based on the modeling be dismissed. Another conclusion that can be drawn from the models is that the expression rate needs around one hour to reach its peak, so any observable changes in protein concentration will be delayed by a little more than one hour.

Sensitivity Analysis

A sensitivity analysis is carried out over the integral model. It aims to see the effect of uncertainties in different parameters on the result curve. Therefore we know which parameters are crucial control points. In the sensitivity analysis, the parameters are added with a random error and put into the model. The method of Latin hypercube sampling is used to generate the error so that the error distribution is uniform over the region.

As the result() shows, the expression rate is most sensitive to the FNR concentration and the expression rate. It is also sensitive to $\alpha_{21}$, $\beta_1$ and $\beta_{31}$ under anaerobic condition. These parameters can be found in the FNR model .

TU-Eindhoven Images sensitivityAnalysis.png
sensitivityAnalysis The Result of Sensitivity Analysis.


The source code of all models can be found here.