Team:USTC-China/Project/modeling

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Contents

results

We have been working hard to model our system.

Fisrt, we will present some basic character of our system

    In a single cell, the system acts like a fast switch upon AHL concentration, on the other hand, cheZ ouput is a slow switch of theophylline concentration.

    We can see that cheZ concentration rises rapidly when AHL concentration rises from 3nM to 4nM. For the switch is so fast that we can use quorum system in our design. CheZ output rises relatively rapid when theophylline concentration is around 210nM.

    For the system without quorum part, If AHL concentration is low, regulate ci protein accumulates, the toggle switch is in the ci state, cheZ production is very low, so the cell can rarely move. And when AHL concentration is high, not enough regulate ci protein is produced, the toggle switch is in the ci434 state, cheZ production is high, so the cell can spend less time tumbling, and will move to the direction where cheZ concentration rises.

Following pictures show how steady-state cheZ concentrations change under conditions of different AHL and theophylline concentrations.

    margin-left:4px S1.png 图片文件夹1

Following pictures show how cheZ concentrations change on time under conditions of different AHL and theophylline concentrations.

    Z a3 t1000.png Z a10 t1000.png 图片文件夹2

Following pictures show how a single cell moves on time under conditions of different AHL and theophylline concentrations in one single round of simulation.

    A3 t1000.png A10 t1000.png</div> 图片文件夹2

Following pictures show how a single cell moves and how cheZ concentration changes on time under conditions of different AHL and gradient of theophylline concentration (30,600) in one single round of simulation.

    AHL = 10 nM

    AHL = 3 nM

图片文件夹3

    Following pictures show 100 cells move under 10nM AHL and gradient of theophylline concentration (25,500).

图片+flash

    For the whole system with quorum part, in the beginning, we assume that the concentrations of all related macromolecules are zero. Cells begin to divide, cell number is growing, and AHL is accumulating, when AHL concentration is high enough, toggle switch in some of the cells turns to the ci434 state, and these cells is moving out. After some time, AHL concentration in these cells will drop, and the toggle switch will most likely turn to the ci state, cells stop moving.

    For this part we assume that numbers of the cells grow under the rate of k=0.97*exp(-t/5), the unit of time is hour.

For no gradient of theophylline
图片
For theophylline gradient (25,500)
图片
results odes parameters and references

odes and equations

Odes and equations

     C1, regulate ci mRNA concentration

     C2, regulate ci protein concentration

     C3, bistable ci mRNA concentration

     C4, total ci protein concentration

     C5, bistable ci434 mRNA concentration

     C6, bistable ci434 protein concentration

     C7, cheZ mRNA concentration

     C8, cheZ protein concentration

     C9, I mRNA concentration

     C10, I protein concentration

     C11, AHL produced

     A, AHL concentration

     For regulatory ci mRNA and protein

     Ode1.PNG

     For Bistable Part

     Ode2.PNG

     For cheZ mRNA and protein

     Ode3.PNG

     For Quorum Sensing Part

     Ode4.PNG

     The real AHL concentration is no the AHL produced. Considering about fast diffusivity of AHL, we assume that external AHL concentration is zero, although it is not quite exact, but it can describe the character of AHL well. That is, for cell i, the compact of cell j is,

     Ode5.PNG

     Tumbling frequency of a cell is determined by its cheYp concentration

     Ode6.PNG

     CheYp concentration is related to cheZ concentration, and for the reaction is so fast, we assume that current cheZ concentration determines current cheYp concentration

     Ode7.PNG

     We assume that cells move at the speed of 0.025um/s on our semisolid plate. For the movement of a single cell, if the cell tumbles, it will stay of the current second, and change its direction later, if not, the cell keeps on moving in one direction.

     Ode8.PNG

     For the gradient of theophylline,

     Ode10.PNG

     For cell number growth

     Ode9.PNG

    
results odes parameters and references

parameters and references

Parameters

Name Value Ref.
k1, max transcription rate of regulatory ci mRNA 0.0933 nM/s 1
k2, translation rate of regulatory ci protein 0.0072 /s 1
k3, max transcription rate of bistable ci mRNA 0.0933 nM/s 1
k4, translation rate of regulatory ci protein 0.0072 /s 1
k'4, translation rate of bistable ci protein 0.048 /s 1
k5, max transcription rate of ci434 mRNA 0.0987 nM/s 1
k6, translation rate of ci434 protein 0.0845 /s 1
k7, max transcription rate of cheZ mRNA 0.0834 nM/s 1, 2
k8, translation rate of cheZ protein 0.1869 /s 1, 2, 4, 7
k9, max transcription rate of lasI mRNA 0.014 nM/s 3
k10, translation rate of lasI protein 0.016 /s 3
k11, AHL synthesis rate 0.06 3
K1, Kd between AHL and Plux promoter 1.6 nM 10
K3, Kd between ci protein and bistable ci promoter 40 nM 1
K'3, Kd between ci434 protein and bistable ci promoter 50 nM 1
K5, Kd between ci protein and bistable ci434 promoter 40 nM 1
K7, Kd between theophylline and RNA aptamer 210 nM 4
n1, Hill co-effiency of AHL and Plux promter 1.6 10
n3, Hill co-effiency of ci protein and bistable ci promoter 4 1
n'3, Hill co-effiency of ci434 protein and bistable ci promoter 2 1
n5, Hill co-effiency of ci protein and ci434 promoter 4 1
n7, Hill co-effiency of theophylline and RNA aptamer 3 7
γ1, Degradation rate of regulatory ci mRNA 0.00434 /s 1
γ2, Degradation rate of regulatory ci protein 30.000935 /s 1
γ3, Degradation rate of bistbale ci mRNA 0.00434 /s 1
γ4, Degradation rate of total ci protein 30.000935 /s 1
γ5, Degradation rate of ci434 mRNA 0.00434 /s 1
γ6, Degradation rate of ci434 protein 0.000935 /s 1
γ7, Degradation rate of cheZ mRNA 0.00434 /s 1
γ8, Degradation rate of cheZ protein 0.00434 /s 1
γ9, Degradation rate of lasI mRNA 0.006 /s 3
γ10, Degradation rate of lasI protein 0.0001 /s 3
γ11, Degradation rate of AHL 0.00038 /s 3
diffu_a, diffusion constant of AHL 10^6 /mm^2 assumption
diffu_t, diffusion constant of theophylline 500, 600 /mm^2 assumption
da, diffusivity constant of AHL 0.23 /s 3
[SetYp], wild type ecoli cheYp concentration 4.4 uM 8
ny, Hill co-effiency of cheYp and cell tumble rate 5.5 9
ky, cheYp phosphorylation rate 3*10^7 /(M*S) 8
k-y, cheYp dephosphorylation rate 5*10^5 /(M*S) 8
[Tp], concentration of wild type chemotaxis phosphorylated receptor Tar 5*10^5 /(M*S) 8
v, cell moving speed 0.025 mm/s 2, assumption
k, cell number growth rate 0.97 /h 6


References

1. the wiki of iGEM09 Peking U team, https://2009.igem.org/Team:PKU_Beijing/Modeling;

2. the E. coli Statistics, http://gchelpdesk.ualberta.ca/CCDB/cgi-bin/STAT_NEW.cgi;

3. Systems analysis of a quorum sensing network: Design constraints imposed by the functional requirements, network topology and kinetic constants, doi:10.1016/j.biosystems.2005.04.006;

4. Molecular interactions and metal binding in the theophylline-binding core of an RNA aptamer; Conversion of the Vibrio fischeri Transcriptional activator, LuxR, to a repressor: Egland, Kristi A. and Greenberg, E. P. Journal of Bacteriology. Feb 2000, p. 805-811: http://jb.asm.org/cgi/content/abstract/182/3/805;

5. A Minimal Model of Metabolism-Based Chemotaxis, http://www.ploscompbiol.org/article/info:doi/10.1371/journal.pcbi.1001004

6. Programmed population control by cell–cell communication and regulated killing, doi:10.1038/nature02491

7. Guiding bacteria with small molecules and RNA, Shana Topp and Justin P. Gallivan. http://pubs.acs.org/doi/abs/10.1021/ja0692480.

8. A model of excitation and adaptation in bacterial chemotaxis, Peter A. Spiro, John S. Parkinson, and Hans G. Othmer. http://www.pnas.org/content/94/14/7263.full.

9. Origins of Individual Swimming Behavior in Bacteria, doi:10.1016/S0006-3495(98)77777-X.

10. Conversion of the Vibrio fischeri Transcriptional activator, LuxR, to a repressor: Egland, Kristi A. and Greenberg, E. P. Journal of Bacteriology. Feb 2000, p. 805-811: http://jb.asm.org/cgi/content/abstract/182/3/805.


results odes parameters and references