IGEM:IMPERIAL/2007/Projects/Biofilm Detector/Modelling: Difference between revisions

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===[[IGEM:IMPERIAL/2007/Projects/Biofilm Detector/Modelling/Construct1|Construct 1]]===
===[[IGEM:IMPERIAL/2007/Projects/Biofilm Detector/Modelling/Construct1|Construct 1]]===
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Here is what our construct looks like composed of biobricks
Here is what our construct looks like composed of biobricks


[[image:ICGEMS_sys_Ptet_luxR_Plux_gfp.png|left|thumb|400px|Ptet promoting LuxR, Plux promoting GFP]] <br clear = "all">
[[image:ICGEMS_sys_Ptet_luxR_Plux_gfp.png|left|thumb|400px|Ptet promoting LuxR, Plux promoting GFP]]
 
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===[[IGEM:IMPERIAL/2007/Projects/Biofilm Detector/Modelling/Construct2|Construct 2]]===
 
The main feature of this construct is that it does not constitutively expresses LuxR and therefore enables us to determine the initial concentration of LuxR
[[image:ICGEMS_sys_Plux_gfp.png‎|left|thumb|200px|Plux promoting GFP]]
 
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Here is a Block Diagram Picture of how construct 1 will work
Here is a Block Diagram Picture of how construct 1 will work
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[[Image: Biofilm-Construct 1.jpg|thumb|left|500px|Construct 1 - LuxR expressed constitutively]]<br clear = "all">
[[Image: Biofilm-Construct 1.jpg|thumb|left|500px|Construct 1 - LuxR expressed constitutively]]<br clear = "all">


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===[[IGEM:IMPERIAL/2007/Projects/Biofilm Detector/Modelling/Construct2|Construct 2]]===
 
The main feature of this construct is that it does not constitutively expresses LuxR and therefore enables us to determine the initial concentration of LuxR
[[image:ICGEMS_sys_Plux_gfp.png‎|left|thumb|200px|Plux promoting GFP]] <br clear = "all">


Here is a Block Diagram Picture of how construct 2 will work<br>
Here is a Block Diagram Picture of how construct 2 will work<br>
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[[Image: Biofilm-Construct_2.jpg|thumb|left|500px|Construct 2 - LuxR not expressed]]<br clear = "all">
[[Image: Biofilm-Construct_2.jpg|thumb|left|500px|Construct 2 - LuxR not expressed]]<br clear = "all">


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*Chemical Equations


 
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*Chemical Equations
*Chemical Equations


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Revision as of 05:54, 28 August 2007

Infector Detector: Modelling


Overview of Modelling

Welcome to our Portal Page for the modelling of Infector Detector.

Infector Dectector (ID) is based on the Quorum Sensing Pathway and our aim in modelling of ID is to determine the concentration of AHL in biofilm we can detect such that we report a visible signal .We are looking at two constructs to emulate the quorum sensing pathway:


Construct 1

The main feature of this construct is that it constitutively expresses LuxR

Here is what our construct looks like composed of biobricks

Ptet promoting LuxR, Plux promoting GFP

Construct 2

The main feature of this construct is that it does not constitutively expresses LuxR and therefore enables us to determine the initial concentration of LuxR

Plux promoting GFP

Here is a Block Diagram Picture of how construct 1 will work

Construct 1 - LuxR expressed constitutively

Here is a Block Diagram Picture of how construct 2 will work

Construct 2 - LuxR not expressed

  • Chemical Equations
  • Chemical Equations

17.08.07 Modelling General Concerns

For protocols to figure out :

  1. Degradation terms:GFP,LuxR,AHL - want expt to find delta as a function of chassis
    • If we put protease inhibitors in the mixture and can we assume negligible degradation for GFP and luxR, not sure about AHL have to look in literature for that.
  2. What is the visual threshold of [GFP] - want expt to find this
    • Do you need to do it for GFP or just for the final reporter used, which is dsRED
  3. What is the concentration of promoters - is this chassis dependant ?
    • You know - the weight of DNA added, and the mass of each plasmid. Knowing that there is only one promoter on each plasmid, you can calculate the concentration of promoters.
  4. Activation/Response Time of Plux (F2620)?
    • You might want to check the part F2620, not sure if the information is useful, or valid for in vitro.

(Protocols) Construct 1 specific:

  1. What is the lifespan of the whole system?
  2. Can we get steady-stateof LuxR? - When will this happen ? - Before cell dies ?
  3. Having reached steady state is there enough E left to express [GFP]

(Protocols) Construct 2 specific:

  1. Can we obtain purified LuxR to be injected into System - protocol for prep of LuxR
  2. Protease inhibitors available?
    • Yes, in homemade extract. For commercial extract, still waiting for reply from promega.
  3. How long will it take to get construct 2 ready ?
    • Week 8, earliest (unfortunately)

For modelling to figure out :

  1. K-values for rxn pathway
    • k5/k4 = 5*10-10M [source: pmid=17400743]
  2. Response of Biofilm : Is [AHL] constant ?
  3. Simulation of [LuxR] vs. Time
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