Team:Colombia/Modeling/Stochastic

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Stochastic Model

The previous sections showed how to know the mean behavior of the system for one cell, but this is just an average of the total proteins within the cell. All the biological systems are controlled by probability events. The cell is a huge space where there are a lot of small molecules, if we want a biological process to happen, two of this little molecules have to find themselves between million of other molecules in a huge pool. Also there is a possibility that a cell may need more concentration of a promoter’s activator while other may need less if the day is sunny but if is cloudy the second cell may need more. The differential equations don’t take into account these uncontrollable events that can change the response dramatically.

If we look only one cell, with all the uncontrollable events this may not behave like we want and the system may not respond or even worse the probability of dying exist and our cell may die. But dealing with one cell is not real, we always work with hundreds of cells. Within this population some cells may no produce the expected response but the others will and the average of cells would be able to respond to the presence of the pest.

The stochastic algorithms are a way to model these probability events within a population. This simulation are made in order to confirm that the system dynamics are robust and consistent and show us if the response is still behaving like we want after taking probabilities considerations. We use the Gillispie method to develop our model. Here is a brief explanation of how it works:

The complete method consists of eight steps.

1. Define the number of cells.
2. Define the time of the simulation
3. Define and name all the constants involved.
4. Define creation and destruction expression for each substance involved: The differential equations in this part have to be divided in two, the creation and the destruction expression.
5. Apply Gilliespie algorithm:
   1. Calculate the sample space of the analysed system: This is the sum of all the changes presented at specific time t.
      
   2. Calculate time distribution that depends on a random number between 0 and 1.
      
   3. Calculate which event occurs: The Gillespie algorithm does not consider simultaneous events, it says that each time only one event occurs. In our case the events are the creation or destruction of one protein. Each event has a probability of of occurrence within the sample space between 0 and 1. To know which event occurs at the time t+1 we take into account the random number use for the time distribution and look for the event that has this probability of occurrence . For example if you see the sample space figure below, there are 5 possibles events with their probability; if the random number is 0.4 then A is gonna be destructed but if the random number is 0.55 then B will be created.
      
6. Take the outputs from the simulation and convert them into regular interval vectors.
7. Obtain the Gilliespie function mean values.
8. Plot the obtained functions.

Results

The mathematical model should help the experimental design to optimize the circuit and our case was not the exception. The picture below shows the original design of the circuit.

After doing the simulation for the differential equations we have to make little changes to the proposed system:

1. As you can see there was an unknown promoter for LuxR. First we decided that it was a constitutive promoter but the response curves of the system were not consistent with the reality (LuxR had giant concentrations and the salicylic acid never went up). We wanted this protein to interact with LuxI and turn on the response, so we thought that it may need to be in a similar concentration of LuxI. Then we put it under the same promoter, hence the two proteins will be promoted at the same time.
2. Our desired response is the increase of Salicylic Acid when a pest gets near the bacteria. With the original system the salicylic acid increased but not as much as we wanted, so to achieve this goal we tried putting the promoter activated by Lux next to the CI promoter to see if there was an increase. After running the simulation we discovered that this solution optimized the increase of salicylic acid in the response.
3. Looking for the right set of parameters we came to the conclusion that the hill constant k (Concentration of the substrate when the the rate of production is half of the maximum production rate) for the promoter activated by Lux had to be 4 times greater than the hill constant for the CI promoter. Which has biological sense; the Lux promoter came from a quorum sensing system, so it needs high concentration of activator because it informs the promoter that there is high cell density. On the other hand the CI promoter box came from a bacteriophage and is used to attack the bacteria as quickly as possible, so it does need small quantities of protein to fully activate its system.

The new system is showed in the picture below:

Differential equations results

Although the screening of the parameters could not be completely done, we made a manual search for them and found a set that makes the system behave as expected. Here we present the mean response of all the substances in our biological system for one cell. The impulse of the pest was made during the times 10-20.

Ralstonia

As you see below, when the system is under the presence of 3-OH-PAME the sensor is phosphorylated really fast and the complex phcR-phcA liberates the activator which has a peak and the goes a little down because is with the promoter and its not free. After the impulse is gone everything goes back to normality.

The LuxI- LuxR System shows and increase after it is activated by phcsA

Now, looking at the species of interest, we can see how the antitoxin has greater concentration than the toxin when the 3-OH-PAME appears, this means that the cell is awake and can produce proteins. On the other hand, the Salicylic acid has an increase of almost two fold.

Rust:

When the system is under the presence of chitin you can see how the positive feedback of the chitoporin and chitinase works and make their concentration increase. This has as a consequence the increase of monomers of chitin and the liberation of the sensor that is gonna activate the LuxI and LuxR promoter.

Like we see with the Ralstonia systema the Lux system's concentrations increase when their promoter is activated. The complex LuxI-LuxR has a peak and then goes down a little because it is busy activation of CI and Salicylic Acid.

The compounds od interest behave just like expected. Like in Ralstonia the cell is awake when the chitin is present and the Salicylic Acid has a two fold increase. It is important to see that this system takes more time to go back to the steady state than the Ralstonia's system.