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Team Colombia @ 2012 iGEM

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Parameters of the equations

When we want to model a biological process, it is necessary to write the differential equation that model the system which requires a number of constants. If the real value for the constants are unknown, the system can not have any biological sense. These entries are called parameters and they are crucial elements in the mathematical model made in this project.

There are three possible ways to find this parameters:

i) Literature. There are a lot of studies trying to find biological parameters, such as basal rate of protein production, kinetic constants, Monod's constants, etc. Moreover, there are so many biological systems and only a few of them have been characterized. Thus, it is difficult to find the parameters that are needed.

ii) Experimental way. If an experiment is made using the biological system of interest, it is possible to find the parameters for the equations that models the whole system. For this project, it was necessary to model the biological system first. Thus, experiments couldn't be performed to find the constant for the differential equations.

iii) Screening of parameters. Sometimes we don't have the exact number that we need, but we have a rank where it could be or the parameter for a similar biological system, then we can perfom a screening of parameter, where we try to find the value that perfectly fits the reponse of our circuit.

How did we do it?

For our biological system we use options i) and iii). In the literature it was possible to find the parameters for the complete CI activation box and for the rest of values we found an aproximately rank where they could be, so we proceeded to step iii).

We used a lot of resources and methods to approximate the limits for this ranges here is its explanation:

a.Basal levels of the proteins:

To determine a range in which this value we described mathematically a very simple process:

Where αo is the basal level, γ is the protein parameter for degradation and P is the protein concentration, now with this, we can assume that in steady state conditions we have that dP/dt= 0, then:

But γ is approximately 1/T, having that:

To establish the range we assumed T as φ and we looked for a normal range of concentration of a protein in a cell [http://bionumbers.hms.harvard.edu/bionumber.aspx?&id=104520&ver=10&trm=protein]. Another important aspect we took in count is that three of the proteins where constitutive because they all were in the same promoter and RBS, so we divided the basal levels in two, one for the basal proteins and other for the constitutive proteins, now with this, the following ranges where defined:

Basal proteins range (LuxR, LuxI, HipB and Salicylic Acid):

Constitutive proteins range (Chitinase, Chitoporin and CBP):

Range: 0.9-1.4µM φ -1

By other part the basal production of HipA is approximately two times HB’s production which was an aspect we took in count.

b.Protein degradation:

One of the facilities of using for the values related with time the E.Coli’s lifetime is that we can establish easily the protein degradation, taking in count that a determined amount of proteins is always destructed each time our unit time is completed, we defined the protein degradation for almost all values as follows:

Again we can found that there is a special case, the degradation of HB is greater so we assigned it a value of 4/φ.

c. Reaction constant:

This value can vary a lot depending of the process we are describing, fortunately we found an article that describes how to approximate this value [http://www.biokin.com/dynafit/scripting/html/node23.html#SECTION00431000000000000000 2] so we took the given approximation and turned it into our units establishing a range we considered prudent.

Range: 500-1000µM-1sec-1

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First of all, we looked for some reference in different data sources where we found the coefficient of CI, now with this, we decided to approximate a range taking this value as a reference.

Once the ranks of the parameters were set, we proceed to do the screening. We tried a lot of techniques and most of the failed, here we present the steps of the succesful one:

1.Sensitivity Analysis

Now we have an idea of which parameters affect the response the most. Although we still don't know what is the exact value of the parameter we know how the system is supose to response.With this two things we can proceed to step 2.

2. Optimization of parameters

A process of optimization takes a function and maximizes o minimizes changing some variable of it. The changing variables are named optimization variables and function is called objective function. If we want to have some limitations or behaves with the variable we can add restrictions to the system, and the function will be optimized without breakinf this limitations.

In our case the objective function is a minimum difference of squares between the points of our expected behaviour and the behaviour of the equations with a set of optimization variable. When the distance between these points is minimun the parameters are found!!!

3.Screening

If we have a set of parameters why do we do a screening?

In the last step we found a set of parameters that give the expected response of the system. But this is only a point.....What if are there more points? Does the optimization method know if these parameters are real or have biological sense?.. We only take into account one expected response, are there similar behaviours of the system with the desired response?

To answer this questions we perfom a sceening of the parameters. This method tries different combinations of parameters and see if some conditions are accomplished. The ranks we use to make this screeining is not the original one!!!!