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Team:Imperial College London/Modelling/Protein Display/Objectives
From 2010.igem.org
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| - | The motivation to develop this model came from our design process. The idea of having surface proteins that could be cleaved and then activate the receptor was very innovatory. However, with this new | + | The motivation to develop this model came from our design process. The idea of having surface proteins that could be cleaved and would then activate the receptor was very innovatory. However, with this new approacha few questions arose that could not be answered without using computer models. Hence, the following aims for this model were specified: |
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<li>Determine the concentration of Schistosoma elastase or TEV protease that should be added to the bacteria in order to trigger a response. This should allow us to correlate the required concentration for the activation with the concentration of Schistosoma elastase in the water.</li> | <li>Determine the concentration of Schistosoma elastase or TEV protease that should be added to the bacteria in order to trigger a response. This should allow us to correlate the required concentration for the activation with the concentration of Schistosoma elastase in the water.</li> | ||
Revision as of 13:33, 27 October 2010
| Modelling | Overview | Detection Model | Signaling Model | Fast Response Model | Interactions |
| A major part of the project consisted of modelling each module. This enabled us to decide which ideas we should implement. Look at the Fast Response page for a great example of how modelling has made a major impact on our design! | |
| Objectives | Description | Results | Constants | MATLAB Code |
| Objectives |
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The motivation to develop this model came from our design process. The idea of having surface proteins that could be cleaved and would then activate the receptor was very innovatory. However, with this new approacha few questions arose that could not be answered without using computer models. Hence, the following aims for this model were specified:
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