Team:Wageningen UR/Project/ModelingProj1

Mathematical model of the Hasty construct

Since our bio bricked oscillatory system is based on the circuit published by Danino et al. in the paper “A synchronized quorum of genetic clocks”, in our team commonly referred to as the "Hasty construct", our first model of the system is a reproduction of the mathematical model in the supplementary information accompanying the publication mentioned. In their simulations, Danino et al. used a set of delay differential equations, which we also used as starting point for our modeling work.

The steps (transcription, translation, maturation etc.) from the luxI and aiiA genes to the corresponding proteins are not modeled separately, but the delay of the correlation between the internal AHL concentration, which triggers the expression of the genes, and the corresponding AiiA and LuxI is simulated by a Hill function which takes the history of the system into account, i.e. the concentration of AHL at the time it binds to LuxR to form the activation complex.

back to top

Writing a modeling tool in matlab

For the first simulations, the same values for the parameters were used as in the cited paper and can be found in the supplementary information. To get graphs representing optimal oscillations, our team created a script for a matlab modeling tool which uses nested for-loops to vary the flow rate and cell density over a range of values. The resulting tool allows the user to enter the range in which the variables should be varied. The tool then iterates over the values and plots graphs of all combinations possible for that range of values.

back to top

Conclusions for our system

The first observation from the model was that, for oscillations to occur, the flow rates may not be too fast, especially at lower cell densities. Since the device used for our system has larger dimensions than the microfluidic device used by Danino et al. the flow rates in the velocities required could not be achieved by varying height differences alone. Further information can be found in the information about the platform used to measure oscillations.

Furthermore, an interesting observation was that applying a flow rate over the cells was not essential to obtain ocillations. Figure 3 shows how, according to the model, oscillations can potentially occur at 0 flow rate. Interesting is that this happens only at high cell densities.

Fig.3: Graphs showing oscillatory behaviour increasing with cell density even when the flow rate is set to 0

Disregarding the strictly mathematical model, some more conclusions were drawn from modeling work as to whether to use a micro-dish or micro-sieve as platform for measuring oscillations. This is described in more detail in the section about the setup of the device.

Expansion of the model for the double tunable oscillatory construct

To accomodate the idea of the double tunable oscillator, the original set of delay differential equations shown above was expanded by two additional differential equations showing the behaviour of the lacI and tetR repressor. The equations for the LuxI and AiiA production were then expanded by a term showing the influence of the corresponding repressor lacI for LuxI and tetR for Aiia respectively. Below the adjusted set of differential equations is shown.

Top: Adjusted set of differential equations for the double tunable oscillator

Since the lacI repressed hybrid promoter used for this system was designed by the Tokyo iGEM 2007 team, the equations were derived according to their model. The tetR repressor was then modeled using the same template.

back to top