Hbsu-xFP

The BioBrick we created to visualize genome shuffling is under the control of an IPTG-inducible promoter. Normally a repressor protein is bound to it, preventing gene transcription. However IPTG can binds to the repressor, changing its shape and removing it from the promoter, allowing expression and production of HBsu-xFP. Using BioNetGen we attempted to model this system, and see if we could predict the time it took for gene expression to start, given initial concentrations of IPTG. As we had no access to Western Blotting or other techniques to determine protein production experimentally, we also attempted to link fluorescence to the average molecule numbers our model predicted.

<a href="https://static.igem.org/mediawiki/2013/b/bb/Hbsu_model.txt" target="_blank">The BioNetGen file </a> (in .txt format, if you'd like to try it out just change the extension to .bngl)

The model was simulated stochastically 25 times at 6 different initial concentrations of IPTG: 0mM, 0.05mM, 0.1mM 0.2mM, 0.4mM and 0.8mM, as these were the concentrations used experimentally. The results for at each concentration were aggregated and averaged using R and graphed against the measured intensity of the HBsu-sfGFP/RFP fluorescence at each concentration.

This fluorescence was calculated using imageJ. As shown in Figure (), initially we used the line selection tool to drew across the cell and measure its mean fluorescence. With mean background fluorescence then measured as a control. To get a Corrected Total Cell Fluorescence (CTCF) for each cell, the mean background fluorescence was deducted from the mean fluorescence of the cell. This was done for 20 cells at each IPTG concentration. This showed that our model predicted the time taken for IPTG to bind to the repressor and allow expression of the BioBrick with reasonable accuracy. Fluorescence was measured experimentally at 0,10,30,60,120 and 240 minutes.