Team:Imperial College London/Drylab/Protein Production

From 2009.igem.org

(Difference between revisions)
(Conclusion)
Line 37: Line 37:
[[Image:II09_SIm_main_prot.jpg]]<br><br>
[[Image:II09_SIm_main_prot.jpg]]<br><br>
<html><a href="https://2009.igem.org/Team:Imperial_College_London/Drylab/M1/Protein_production/Simulations"><img style="vertical-align:bottom;" width=90px align="left" src="http://i691.photobucket.com/albums/vv271/dk806/II09_Learnmore.png"></a></html>&nbsp; about the simulations! <br><br><br>
<html><a href="https://2009.igem.org/Team:Imperial_College_London/Drylab/M1/Protein_production/Simulations"><img style="vertical-align:bottom;" width=90px align="left" src="http://i691.photobucket.com/albums/vv271/dk806/II09_Learnmore.png"></a></html>&nbsp; about the simulations! <br><br><br>
-
*The effects of IPTG toxicity were investigated and we found that for these concentration ranges, IPTG is not toxic to cells. See the pdf of results for further details:[[Media:II09_IPTG_growth.ogg]]
+
*The effects of IPTG toxicity were investigated and we found that for these concentration ranges, IPTG is not toxic to cells. See the pdf of results for further details:[[Media:II09_IPTG_growth.ogg | IPTG growth curves]]
-
*The constants in this model are arbitrary. We justify our usage of these values with a more detailed dynamical analysis of the system, which shows that it can only have fixed points[ref Strogatz]. [[Media:II09_Prot_stability analysis.ogg]]
+
*The constants in this model are arbitrary. We justify our usage of these values with a more detailed dynamical analysis of the system, which shows that it can only have fixed points[ref Strogatz]. [[Media:II09_Prot_stability analysis.ogg | System stability analysis (read about the equations before opening this file, it's intimidating!)]]
===Conclusions===
===Conclusions===

Revision as of 18:51, 7 October 2009



Protein Production

Based on the Genetic circuit, a LacI-IPTG inducible promoter is responsible for kickstarting the production of the drug.

  • In the absence of IPTG, LacI represses the production of the drug (Cellulase or PAH)
  • When IPTG is introduced, the LacI repressing pathway is “de-repressed”, and some output protein is produced.
II09 NoIPTG yesIPTG.jpg


Contents

Our goals

The modelling aims to provide an overview and better understanding of the M1 system’s function by:

  • Characterizing the system.
  • Modeling to account for several factors that may reduce/hinder the production of the protein drug such as:
    • Lac promoter leakiness
    • IPTG toxicity
    • Stability of output protein


This module is an integral part of the design, as large-scale commercialization of the drug of interest depends on finding the optimal conditions for protein production.

  about the model assumptions and predictions!


The System

There are 6 differential equations that describe the behaviour of this system.
  about the equations and what they mean!


Summary of simulation results

  • When we introduce IPTG into the system, it temporarily removes LacI from the system. Hence, during this period of time, we produce the drug of interest.
  • When the effects of IPTG wear off, the system returns to equilibrium.
  • The more IPTG we add in, the higher the amount of output protein.

II09 SIm main prot.jpg

  about the simulations!


Conclusions

NOTE: These will be better understood once the reader has gone through the details ("Learn More").

  • The greater the strength of the Lac promoter, the greater the repressive action of LacI prior IPTG induction.
  • The greater the Lac promoter leakiness (kleak) the greater the basal amount of expression of protein of interest, prior IPTG induction.
  • The greater the amount of IPTG introduced, the greater the size of the bump in production of protein of interest.
  • Here we assumed that the range of IPTG we have introduced is non-toxic for our cells. Growth curves will tell us whether IPTG does limit cell growth at the ranges we are interested in.



Mr. Gene   Geneart   Clontech   Giant Microbes