Team:NCTU Formosa/modeling

From 2013.igem.org

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(Ecolightuner Simulation)
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===Ecolightuner Simulation===
===Ecolightuner Simulation===
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====37 °C RBS Controlled sRNA Inhibition Circuit====
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<p>Figure 1 shows the essential constituent of our E. colightuner. To save our efforts experimenting with this essential engine of E. colightuner, we built a model beforehand to help us evaluate its practicability. Our model is consisted of three components A, B, C, and D
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<p>Figure 2 is the overall picture of our component A. Notice that component A is built from similar biobricks as our E.colightuner. The only difference between the two is the promoters used. Both Preds of E.colightuner are substituted with Pcons in component A. With that said, by taking the difference in the strength between Pred and Pcons, into calculations, we would be able to model out E. colightuner with component A. Before that, however, we would have to first build a model for component A.
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<P>To build a model for component A, we combined component B and C. As you can in component B shown in Figure 3, it does not include Plux and luxR like component A. By assuming that when luxR is expressed, Plux would immediately reach its full strength, however, we can consider luxR and Plux pair as simply a Pcons,that is constitutively activated. From this perspective, component A and B are the same, except that component A is also effected by the translational efficiency of 37oC RBS. Component C in Figure 4 is the model for 37oC RBS. So by multiplying component C and component B, we would be able to obtain a model for component A.
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<p>In order to increase the accuracy of our component A model, we used ANFIS to fit our modeling result with the actual experimental data of our component A. By doing this, we obtained a new modeling curve for component that is more precise and accurate, shown in Figure 5.
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<p>As mentioned above, we needed to take the effect of Pred into account before we could a model of E.colightuner based on component A. Component D in Figure 6, is the model of Pred built in a similar way as component A model. We first built a model for Pred and fitted it into the actual experimental data. Having both precise model for component A and component D, we simply had to multiple them to obtain the final model for our E.Colightuner.
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====sRNA Constant Inhibition Circuit====
 
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====Red Promoter and 37 °C RBS Controlled sRNA Constant Inhibition Circuit====
 
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Revision as of 13:45, 28 October 2013

Modeling

Modeling was our first step forward. When validated with our experimental data, modeling is also a verification of the accuracy of our experiments.

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Contents

MATLAB Introduction

MATLAB (matrix laboratory) is a numerical computing environment and fourth-generation programming language. It is developed by MathWorks, a company in United States. MATLAB allows matrix manipulations, plotting of functions and data, implementation of algorithms, creation of user interfaces, and interfacing with programs written in other languages, including C, C++, Java, and Fortran. Although MATLAB is intended primarily for numerical computing, an optional toolbox uses the MuPAD symbolic engine, allowing access to symbolic computing capabilities. An additional package, Simulink, adds graphical multi-domain simulation and Model-Based Design for dynamic and embedded systems.


Fig.  Images of MATLAB

ANFIS Introduction

Adaptive-Network-Based Fuzzy Inference System, in short ANFIS, is a power tool for constructing a set of fuzzy if-then rules to generate stipulated output and input pairs. Unlike system modeling using mathematical rules that lacks the ability to deal with ill-defined and uncertain system, ANFIS can transform human knowledge into rule base, and therefore, ANFIS can effectively tune membership functions, minimizing the output error.

Single Unit

Red Promoter

Lux Promoter

We did the following modeling based on the data obtained from Imperial 2007 iGEM team. The data notes the strength of Plux under different concentrations of AHL and different time frames.

Figure 2. the biobrick to test expression of the lux promoter

Using ANFIS to train 76 sets of data and to test 20 sets of data, we ontained Figure 3. It shows that our training data exhibits a similar trend as the testing data, even though the computer has no based knowledge of the trend. This simply means that our modeling has successfully simulated the actually data.

Figure 3. The training and testing data using ANFIS system

Figure 4 is the resultant graph from input 1(time) and input 2(AHL concentration). According to this graph, we can observe the fluorescence has two peaks about AHL concentration(at concentration of 4 nM and 40 nM). That means we could achieve our regulation goal with little AHL. Also, pleas note that there is more output as time passes.

Figure 4. Input 1 is time(min), input 2 is AHL concentration, and output is fluorescence.


37 °C RBS

We used Figure 1 biobrick to model our 37oC RBS's function at different temperatures.

Figure 1. The biobrick used to test the temperature-regulated RBS function

First, we did a experiment that test the fluroscence at different temperature and different time. Then we input these sets of data to ANFIS system to model the graph like Figure 2.

Figure 2. Input 1= Time (hr), Input 2= Temperature (degree Celsius), Output = Normalized expression (AU).


From Figure 1, the maximum output is obtained at 37 oC. Under the same time frame, the output (the normalized expression of the reporter gene) is maximized at 37 oC while minimized at 25 oC. There is a dramatic decrease in the output below 30 oC and the outputs around 37oC are much higher. This modeling demonstrates that using 37 oC RBS is a plausible approach for achieving gene expression through temperature.

Ecolightuner Simulation

Figure 1 shows the essential constituent of our E. colightuner. To save our efforts experimenting with this essential engine of E. colightuner, we built a model beforehand to help us evaluate its practicability. Our model is consisted of three components A, B, C, and D <p>Figure 2 is the overall picture of our component A. Notice that component A is built from similar biobricks as our E.colightuner. The only difference between the two is the promoters used. Both Preds of E.colightuner are substituted with Pcons in component A. With that said, by taking the difference in the strength between Pred and Pcons, into calculations, we would be able to model out E. colightuner with component A. Before that, however, we would have to first build a model for component A. <P>To build a model for component A, we combined component B and C. As you can in component B shown in Figure 3, it does not include Plux and luxR like component A. By assuming that when luxR is expressed, Plux would immediately reach its full strength, however, we can consider luxR and Plux pair as simply a Pcons,that is constitutively activated. From this perspective, component A and B are the same, except that component A is also effected by the translational efficiency of 37oC RBS. Component C in Figure 4 is the model for 37oC RBS. So by multiplying component C and component B, we would be able to obtain a model for component A. <p>In order to increase the accuracy of our component A model, we used ANFIS to fit our modeling result with the actual experimental data of our component A. By doing this, we obtained a new modeling curve for component that is more precise and accurate, shown in Figure 5. <p>As mentioned above, we needed to take the effect of Pred into account before we could a model of E.colightuner based on component A. Component D in Figure 6, is the model of Pred built in a similar way as component A model. We first built a model for Pred and fitted it into the actual experimental data. Having both precise model for component A and component D, we simply had to multiple them to obtain the final model for our E.Colightuner. </div></div>



Reference
  1. iGEM 2007 Imperial https://2007.igem.org/Imperial