Team:Potsdam Bioware/Project/Modeling

Modeling

Modeling

Abstract

Introducion

Modeling is a powerful tool to understand complex interactions or processes. We created a model to illustrate our selection system and to get a better understanding of its behavior under different conditions. Thereby, we wanted to answer two main questions:

1. At which time point selection is successful?
2. How many antibody presenting cells and how many virus particles do we need at the beginning?

To answer these questions we did both deterministic and stochastic modeling using MATLAB. Furthermore, we did a huge parameter analysis for each model to check what kind of influence each parameter has on our selection system.

Simplest Model

Reaction Scheme

We built a simple model of our in vivo selection system which includes the reactions that are the most equivalent to our project. The following scheme (Fig. 1) shows the reactions occurring in our model.

Fig. 1: Reaction scheme of our selection system. Wildtype CHO-cells will be mutated by AID and both will be infected by virus. Mutated cells will be selected via virus due to higher infection rate and because of positive stimulus through virus infection.

Species: V...Virus C...WT-CHO cell presenting antibodies and expressing AID for antibody mutation CV...WT-CHO cell after infection with virus M...Mutated CHO cell presenting more affine antibodies MV...Mutated CHO cell after infection with virus reaction rates: k_div...cell division rate k_divAinf...cell division rate after infection of virus k_death...cell death rate k_deathAinf...cell death rate after infection of virus k_mut...mutation rate (rate to get better antibody) k_intC...infection rate of virus with WT-CHO cells k_intM...infection rate of virus with mutated CHO cells k_loss...loss of viral genes (means: loss of stimulus due to virus infection)

Our system starts with the antibody presenting cell exhibiting a cell division rate (kdiv) and a cell death rate (kdeath). Due to expression of AID the antibodies get mutated and with a particular rate (kmut) we get a mutated cell presenting more affine antibodies. Thereby, the virus infection is changed and is able to trigger the selection of mutated cells. We can distinguish between two different cases.

Within the first case, the infection rate of the virus to the mutated cell (kintM) is improved compared to the infection rate to WT cell (kintC). In this case through the virus infection a positive stimulus can be mediated, resulting in both a higher cell division rate (kdivAinf) and/or a lower cell death rate (kdeathAinf).

In case two, the infection rate of the virus to the mutated cell is decreased compared to the infection rate to WT cell C (kintM < kintC). Hence, through the virus infection, a negative stimulus can be mediated, resulting in a lower cell division rate (kdivAinf) or a higher cell death rate (kdeathAinf) or even both. The stimulus due to virus infection gets lost while the process proceeds (kloss). This means that the virus infection is steadily required for those stimuli.

(Due to the experimental observation which show that without an antibody no infection can be seen, we assume that with a better antibody on the cell surface the infection rate by the virus is improved compared to the WT cell. This means we should apply a positive selection system. For this we use antibiotics as selection pressure and antibiotic resistance as positive stimulus through virus infection. Therefore, for modeling we used low cell division rate compared to cell death rate and a high cell division rate after virus infection.)

Deterministic Model

For deterministic modeling we write the reactions as ordinary differential equations (ODE´s) (see Fig. 2) and solved them using MATLAB. Because we only had marginal information about parameter values we estimate them and did a large parameter analysis (see below).

Media:UP12-det-simplemodel.m

ODE´s

Figure 2: Ordinary differential equations for our selection system.

Results

For calculation in MATLAB we used the following parameter values as reference state. In figure 3 time dependent concentrations of each species are shown.

Figure 3:Solution of differential equations. Cell or virus particle concentrations is plotted against time.

Reference state: initial state: V0=10000 virus particles/mL C0=1000 cells/mL CV0=0 M0=0 MV0=0 parameters: par.k_div=0.02 1/h par.k_divAinf=0.1 1/h par.k_death=0.03 1/h par.k_deathAinf=par.k_death par.k_mut=1e-5 1/h par.k_intC=1e-6 mL/(h*virus particles) par.k_intM=1e-4 mL/(h*virus particles) par.k_loss=0.2 1/h

We start with a 10-fold higher concentration of virus (shown in dark blue) compared to WT cell (shown in green). Concentration of WT cells decreases because of cell death due to antibiotic pressure. Virus concentration decreases because of infection of cells. WT cells were only marginal infected resulting in low concentration of infected WT cells (shown in red). After about 100 h mutated cells arose and were directly infected, because of high infection rate and high virus concentration. This leads to increased concentration of infected mutated cells and mutated cells respectively, due to stimulus of virus infection (antibiotic resistance). From that time point concentration of virus decreases rapidly and gets down to zero at about 200 h. Because of the lack of virus, cells were not infected and will get no positive stimulus. Due to continuous antibiotic pressure, cell concentration of both mutated and WT cells decreases.

To act against these decreases we performed two time steps shown in figure 4. In the first time step high selection pressure via antibiotics was applied. After successful selection, the antibiotic pressure was removed (e.g. by medium exchange) and therefore cell concentration increases due to higher cell division rate than cell death rate. Media:UP12-det-twostepmodel.m

Figure 4: Solution of differential equations for two time steps. After 250 h cell death rate is set down to 0.01 1/h.

Parameter Analysis

Because we had only marginal information about parameter values we did a large parameter analysis. We wanted to know how each parameter influences the selection system. Therefore, we looked at the influence on success of selection and the influence on time scale. For this analysis we observed the ratio of mutated cells to WT cells (ratio of M to C). For a successful selection the ratio of mutated cells to WT cells should be higher than one and as high as possible.

Media:UP12-det-parameteranalysis.m

One dimensional (1D)

For one dimensional analysis we changed each parameter holding all other parameters constant at reference state and observed the ratio of mutated cells to WT cells. Following results were obtained:

initial concentration of wt cells initial concentration of virus cell death rate cell division rate cell division rate after infection infection rate for wt cells infection rate for mutated cells loss of viral genes mutation rate

Figure 5: One dimensional analysis of all parameters. The ratio mutated to wt cells is plotted against the parameter value. A high ratio is related to successful selection.

These parameter analysis gives us different information about the behavior of our selection system. Following highlights we can mention. For some parameters there is a optimum range of parameter value for our model. One example is the initial virus concentration. Both too less and too excessive concentration prevent successful selection. Other parameters should be high or low. The mutation rate for example should be high to get a successful selection. Also important is the infection rate of the virus. The infection rate for mutated cells must be higher than the infection rate for wt cells to get a positive result. A strange behavior shows the initial wt cell concentration. The model predicts that the lower the concentration the better the selection. This is not biological reasonable and can be due to deterministic calculation. Therefore we run stochastic calculation of our model (see below).

Two dimensional (2D)

For two dimensional analysis we changed two parameter holding all other parameters constant at reference state and observed the ratio of mutated cells to wt cells. Two dimensional analysis can so show the influence of two parameters among each other. The analysis of initial virus concentration and wt cell concentration shows that there is a optimal virus concentration and the concentration of wt cells should be low (Fig. X). That the wt cell concentration should be very low make biological no sense at all. The infection rates of virus shows us that there is a wide range which leads to successful selection (see Fig. X). But if infection rate for wt cell is too high and infection rate for mutated cell is too low we got no successful selection.

Fig. 6: Ratio mutated to wt cell concentration is plotted against initial wt cell and virus concentration.

Fig. 7: Ratio mutated to wt cell concentration is plotted against infection rate for mutated and wt cell.

Influence on time scale

To find out which parameter has an influence on time scale, we observed the ratio of mutated cells to wt cells over the time changing only one parameter. If the parameter has an influence on time scale, changes in the ratio of mutated cells to wt cells should be observed earlier or later. Following results were obtained:

We observed that different parameters have different influence on time flow of our selection systems. A high influence on time flow have the mutation rate (k_mut), the infection rate for mutated cells (k_infM) and the cell division rate after virus infection (k_divAinf). On Figure x for example you can see that the higher the mutation rate the earlier we get a higher ratio of mutated to WT cells. This means selection of mutated cells presenting a high affine antibody happens earlier. Also the higher the infection rate for mutated cells or the cell division after infection, the earlier we get a selection success (Figure x and y).

Figure 8: Influence on time scale of mutation rate. Ratio mutated to wt cell is plotted against parameter value and time. Figure 9: Influence on time scale of infection rate of virus for mutated cell. Figure 10: Influence on time scale of cell division rate after virus infection.

The parameter k_loss have only low influence on time flow of selection system (see Figure x). The higher rate of the loss of viral genes (the positive signal), the later selection is successful. The cell division rate (k_div), the cell death rate (k_death) and the infection rate with WT cells (k_infC) are time independent (see Figure x). These parameters have only an influence on success of our selection system, but not on the time point when selection is finished.

Figure 11: Influence on time scale of loss of viral genes

Figure 12: Influence on time scale of cell division rate

Figure 13: Influence on time scale of cell death rate

Figure 14: Influence on time scale of infection rate of virus for wt cell.

Stochastic Model

Stochastic modeling is necessary if one or more species occur in low amounts. In this case reactions are random events that lead to fluctuating concentrations of species which can be characterized by different results in several experiments or runs, respectively. In our selection system we get only low amount of mutated cells due to low mutation rate. Because of this and because of some peculiar behavior of the deterministic model we did stochastic modeling. For this we used the “simbiology” - tool of MATLAB. We built our model in the “simbiology” - tool and calculated stochastic kinetics using the stochastic simulation algorithm (SSA). This algorithm efficiently generates individual simulations that are consistent with the chemical master equation (CME). The greatest advantage of this algorithm is the precision. [1]

We used the same parameters like in deterministic modeling.

Results

In figure x the concentration of each species is plotted against the time. We see nearly the same results compared to deterministic model. The concentrations of virus and WT cells decrease. From a certain time point the concentrations of infected mutated cells and mutated cells increase while virus is available. When virus concentration becomes zero, the concentrations of infected mutated cells and mutated cells decrease.

Figure 15: Solution of CME with stochastic simulation algorithm (SSA).

The difference between deterministic and stochastic model becomes obvious when we run the stochastic calculation several times (see figure x). Figure x shows that the time point when mutated cells were selected and their concentration was greater than non-mutated cells, differ in large scales. Furthermore, in some runs mutated cells did not arise, meaning that sometimes the selection was not successful. This is a typical result and can be explained by the stochastic behavior. Because of low concentration of mutated cells sometimes they become extinct by random events and no selection takes place.

Figure 16: Example of ensemble run of our selection system. After 10 runs we got 7 successful selections

Parameter Analysis

For stochastic modeling we also did parameter analysis for both one and two dimensional. We change one or two parameters while holding the other parameters constant and run the calculation 3x100 times counting the successful selections. As a successful selection we defined a ratio of mutated cells to WT cells greater than 1. In Figure x you can see the results for 100 runs for different initial virus or wt cell concentration. For initial virus concentration you can see that at 100 virus particles per mL we got 0 successful selection. If we increase the concentration we got more positive results, but if we increase up to 100000 virus particles per mL the percentage of successful results decreases. Similar results we got for initial wt cell concentration.
Media:UP12-stoch-parameteranalysis.m

initial virus concentration: 100 1000 10000 100000

initial wt cell concentration: 10 100 1000 10000

Figure 17: 100 runs of stochastic model with different initial virus or wt cell concentration. Hover with cursor over the different concentrations to see results.

One dimensional (1D)

With the ensemble runs we count the successful selection and plotted the percentage of successful selections against the parameter values for one dimensional analysis.

initial concentration of wt cells initial concentration of virus cell death rate cell division rate cell division rate after infection infection rate for wt cells infection rate for mutated cells loss of viral genes mutation rate

Figure 18: One dimensional analysis of all parameters. The percentage of selection success is plotted against the parameter value.

The one dimensional analysis shows nearly the same results like for deterministic model. The important difference is that initial wt cell concentration should not be to low. So there is an optimum wt concentration to get high probability for successful selection. This you also can see in two dimensional analysis together with initial virus concentration (see below).

two dimensional

There are optimal concentrations for virus and wt cells to get the highest probability for successful selection (see Fig. 19). Both too high and too low concentration decrease the probability to get a positive result. But this optimum is influenced by several other parameters. For example if we increase the cell death rate we can increase the initial wt cell concentration (see Fig. 20). Through the high cell death rate, which is closed to high selection pressure, the mutated cells get a better chance to win recognition against wt cells.

Figure 19:Dependency of success form initial virus and wt cell concentrations. Figure 20:Influence of cell death rate on optimal initial wt cell concentration.

Summary

With stochastic calculations we got the best results. The deterministic modeling had some strange behavoir, especially in parameter analysis. For example make the deterministic model the prediction that the initial wt cell concentration should be very low, but that is not biological realistic. Therefore stochastic modeling is much better.
Stochastic results showed that the selection is finished on random time points after 100 h or later (see Fig. 16). The probability that selection is finished increases with time. Furthermore, the analysis of initial concentrations of wt cell and virus revealed that there is an optimum for initial concentrations of wt cell and virus (see Fig. 19). Both too less and too excessive concentrations prevent the success of the selection system. This optimum is influenced by the other parameters, but if we can determine some of these parameters we can calculate the optimal concentrations to start our selection.