Team:Imperial College/Genetic Circuit

An accurate mathematical description of the behaviour of the genetic circuit is essential for projects involving synthetic biology. Such descriptions are an integral component of part submission to the Registry, as exemplified by the canonical characterisation of part F2620 (1). The ability to capture part behaviour as a mathematical relationship between input and output is useful for future re-use of the part and modification of integration into novel genetic circuits.

A simple [http://openwetware.org/wiki/Imperial_College/Courses/Spring2008/Synthetic_Biology/Computer_Modelling_Practicals/Practical_2 synthesis-degradation model] is assumed for the modelling of the expression of a protein under the control of a constitutive promoter, with the same model assumed for all four promoter-RBS constructs. The synthesis-degradation model assumes a steady state level of mRNA.

In this case, [protein] represents the concentration of GFP, which will be the reporter protein in our constructs used for characterisation. k₁ represents the rate of synthesis and d₁ represents the degradation rate. We can easily simulate this synthesis-degradation model using Matlab; the ODEs and simulation file can be found in the Dry Lab Appendix.

We can also solve this ODE analytically.

Consider the steady-state behaviour of [protein].

The relationship between the steady-state protein concentration and the parameters can be seen in the parameter scan graphs on the right.

Note from the parameter scan graphs:

• In the case where k₁ = 0, no GFP is sythesised.
• In the case where d₁ = 0, the concentration of protein does not reach a steady state.

From the wetlab experiments it is likely that we will obtain steady-state data for each of the four promoter-RBS constructs. If we assume the same rate of degradation of GFP in each case, we can use the relative steady-state levels of GFP as a proxy for the relative rate of transcription through each promoter. This will help us with the selection of the most appropriate promoter to use for Phase 2. In order to obtain an absolute measure of transcription (as opposed to a relative measure of transcriptional strength) we require constitutive expression in terms of molecules per cell (as opposed to fluorescence in arbitrary units).

Complementary experiments to estimate the rate of degradation of GFP - by terminating transcription - would allow us to estimate absolute rate of transcription through each promoter.

Click here for more detail

A literature search revealed two models of IPTG-induced expression through the Plac promoter. Both models assume constitutive expression of LacI. Before IPTG is added, a steady-state is reached comprising basal (leaky) expression of GFP.

In the simpler model (2) IPTG competes with free promoter for LacI binding, but does not itself bind to the LacI-promoter complex.

Under this model, with all other parameters constant, the steady-state concentration of free promoter and hence the steady-state concentration of GFP are independent of the initial concentration of IPTG. (See time evolution of GFP expression assuming different concentrations of IPTG are used for induction, right.)

The pre-steady-state dynamic behaviour of the GFP concentration will differ with different initial concentrations of IPTG (but the steady-state behaviour will not). Hence, accurate data collection during the pre-steady-state phase is crucial for parameter estimation.

A more sophisticated model allows for interaction between IPTG and the promoter-LacI complex (3). IPTG can bind to the promoter-LacI complex to form IPTG-LacI and free promoter. This eases the repression by LacI and allows transcription of GFP.

Under this model, the dynamic behaviour (whether or not [GFP] attains a maximum higher than its steady-state value) depends on the relative strengths of the kinetic constants describing the interactions underlying the model. Either way, the steady-state [GFP] will vary as a Hill-function dependent on the initial concentration of IPTG; this characteristic can be used to discriminate between the two models.

ODEs and simulation m-files for further exploration of the properties of these models can be found in the Dry Lab Appendix.

>>> Details of equilibria and equations and qualitative discussion of parameter effects >>>

References

1. Canton B, Labno A, & Endy D (2008) Refinement and standardization of synthetic biological parts and devices. - Nature biotechnology 26 (7) 787-793
2. Alon, U (2006) An Introduction to Systems Biology: Design Principles of Biological Circuits - Chapman & Hall/Crc Mathematical and Computational Biology
3. Kuhlman T, Zhang Z, Saier MH Jr, & Hwa T (2007) Combinatorial transcriptional control of the lactose operon of Escherichia coli. - PNAS 104 (14) 6043-6048