Team:Imperial College London/Modelling/Protein Display/Objectives

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|style="font-family: helvetica, arial, sans-serif;font-size:2em;color:#ea8828;" align="right"|[[Team:Imperial_College_London/Modelling/Protein_Display/Detailed_Description | Click here for a detailed description of this model...]]
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Revision as of 00:56, 28 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

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 approach few questions arose that could not be answered without using computer models. Hence, the following aims for this model were specified:

  1. Determine the concentration of Schistosoma elastase or TEV protease that should be added to the bacteria in order to trigger a response.
  2. Attempt simulating how long it takes for the protease or elastase to cleave enough peptides and, hence, trigger the response.
  3. Assess the risk of false positives (i.e. system is activated without the required stimulus).

IC AIP threshold.png
The pink shadow indicates which part of the whole system that the detection model simulates. It includes TEV or Schistosoma protease cleaving the surface protein to activate the receptor.
Click here for a detailed description of this model...
Retrieved from "http://2010.igem.org/Team:Imperial_College_London/Modelling/Protein_Display/Objectives"