This pathway has two inputs, but only has two states: the target gene expressed or not. If Pulseon input signal is greater than pulseoff will lead to Gene of interest expression, otherwise silent.
In order to expand our scope of the filter, we also design the eukaryotic pathway which has the function of corresponding filter/switch. Meanwhile, we also need to understand its working condition clearly.
Modeling
In this pathway, the time of spreading of the substance or each combination/response reaction, compared to the whole time scales (protein), is negligible, so we adopted simplified differential equation to simulate the pathway this time.
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Parameter details
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Fomular
more details
Analysis
We have only on/off states of the eukaryotic system, so the complexity of this model will be lower, but it probably means that the system can have a better stability and robustness, For that reason, we will focus on the sensitivity analysis of parameters, meanwhile, validate designed functions will work out or not.
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Test of filter function
We adopted a simple sine function as input to verify the filtering performance.* (The input signal in the figure is to show the result more clearly so that we have moved the graph. The actual strength is 0.1sin（t）)
We can see that the output signal, which does not contain obvious waveform, is still stable. And the ABF2 phosphorylation/dephosphorylation of the system have played the role as the "capacity" as we analyzed before, so as to improve the filtering effect of the system.
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Parameter sensitivity analysis/robustness evaluation
The main approximate treatment in this circuit should be substrate disaggregation coefficient correction, when SnRK2.2 / PP2Cs concentration is low and supersaturated by the substrate, meanwhile, part of the substrate cannot be catalytic in time. So we mainly analyzed the velocity of substrate（mABF2） producing rate for testing the sensitivity of the parameters, which is named trc1.
Similarly, we keep pathways in the condition of open and choose to change the ratio of signal strength to find out the final expression level and the response time for analyzing.
The expresion level of the final production varies with the changing of trc1, but it still maintains itself in a high expresion level, which has a minor influence on our switching or the filting function.
Even though there exist some twists in the responsing time, all the floating range is still in 10%. And our circuit shows a great stability after we enlarged the numerical value of trc1.
Summery
Our eukaryotic pathway can be worked out as a filter and a swich in a steady way. And the analyzement of sensitivity of parameters also shows that we should use the promoter, which has much bigger velocity of transcription, to help maintain a great robustness.
