Team:Paris/Modeling/Workflow Example

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Revision as of 23:46, 29 October 2008

Characterization Approach : Application of our Generic Workflow on a given Example

Here, we explain the generic protocol that leads to modeling "by characterization", of one of the parts of our system. The chosen example is the activity of the promoter pFliL (that leads to the production of the Fluorescent Protein FP1) in function of the transcription factors FlhDC and FliA . We know that the hexamere FlhD₄C₂ and the protein FliA act both on the promoter pFliL as inducers... how do we evaluate this phenomenon?
As it is illustrated below; starting from molecular reactions (1), we develop a model of our system (2), and then we identify the parameters (3) that need to be estimated. Essentially, it amounts to estimate Promoters Activities as functions of their Transcription Factors. To do so, we propose constructs (4), protocols (5) and programs (6).

CLICK on the images below for further information on each step!

Modelisation	Experiments

By estimating all parameters of every function involved in our Full System, we achieve a "Modular Virtual Lab" of our System with potential predictive capacity.

↓ Details on the Steps ↑

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 {{Paris/Menu}}
-{{Paris/Header|Characterization Approach : Generic Workflow on an Example}}
+{{Paris/Header|Characterization Approach : Application of our Generic Workflow on a given Example}}
-Here, we will explain the generic protocol that leads to the modelisation "by characterization", of one of the parts of our system. The choosen example is '''the activity of the promoter ''pFliL'' ''' (that leads to the production of the '''Fluorescent Protein FP1''') '''in function of the transcription factors ''FlhDC'' and ''FliA'' '''.
+Here, we explain the generic protocol that leads to modeling "by characterization", of one of the parts of our system. The chosen example is '''the activity of the promoter ''pFliL'' ''' (that leads to the production of the '''Fluorescent Protein FP1''') '''in function of the transcription factors ''FlhDC'' and ''FliA'' '''.
 We know that ''the hexamere FlhD<sub>4</sub>C<sub>2</sub>'' and the protein ''FliA'' act both on the promoter ''pFliL'' as inducers... how do we evaluate this phenomenon? <br>
-As it is illustrated below; starting from ''molecular reactions'' '''(1)''', we develop a ''model of our system'' '''(2)''', and then we identify the ''parameters'' '''(3)''' that needs to be estimated. Essentially, it amounts to estimate ''Promoters Activities as functions of their Transcription Factors''. To do so, we propose ''constructs'' '''(4)''', ''protocols'' '''(5)''' and ''programs'' '''(6)'''.
+As it is illustrated below; starting from ''molecular reactions'' '''(1)''', we develop a ''model of our system'' '''(2)''', and then we identify the ''parameters'' '''(3)''' that need to be estimated. Essentially, it amounts to estimate ''Promoters Activities as functions of their Transcription Factors''. To do so, we propose ''constructs'' '''(4)''', ''protocols'' '''(5)''' and ''programs'' '''(6)'''.
 <br>
-<center><span style="color: red; font-weight: bold; font-size: 16">CLICK on the images below for further informations on each step!</span></center>
+<center><span style="color: red; font-weight: bold; font-size: 16">CLICK on the images below for further information on each step!</span></center>
 <br>
 <center>
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 </center>
-Once we got every parameters for every functions involved in our Full System, we have got a "Modular Virtual Lab" of our System that aims to be ''predictive''.
+By estimating all parameters of every function involved in our Full System, we achieve a "Modular Virtual Lab" of our System with potential ''predictive'' capacity.
 <br>