Team:SEU O China/Model

From 2012.igem.org

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In the light sensing model, due to the big influence of light from the outer environment, cell movement has almost nothing to do with final results both in simulation or realistic experiments. As a result, we simplify the movement of cells. However, the movement of cells would no longer be negligible in the afterwards models. Further details on its rules and results to come afterwards.
In the light sensing model, due to the big influence of light from the outer environment, cell movement has almost nothing to do with final results both in simulation or realistic experiments. As a result, we simplify the movement of cells. However, the movement of cells would no longer be negligible in the afterwards models. Further details on its rules and results to come afterwards.
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d) Cell Death
d) Cell Death
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[[File:Seuofun4.GIF|center]]
[[File:Seuofun4.GIF|center]]
*u: AHL density; D: diffusion constant;  q: AHL releasing rate of a single triggered cell; γ describes the decomposition process of AHL; m: total number of cells.
*u: AHL density; D: diffusion constant;  q: AHL releasing rate of a single triggered cell; γ describes the decomposition process of AHL; m: total number of cells.
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'''Simulation Procedure'''
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At the very beginning, AHL density u(r, 0)=0 on the infinite plane. In order to eliminate the asymmetry in the results that might be caused by the asymmetry of the original state, there is only one green cell at first. Choose several separate cells manually to shed light on. With the sliding improvement of the colony from merely one cell, green cells would eventually reach the light area where they would transform into red cells. Red cells begin to release AHL. When the quantity of red cells accumulates to a certain threshold, high density of AHL in certain areas would repress the division of cells and begin to trigger the differentiation of cell and therefore break the symmetry of the colony.
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'''Results'''
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----
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'''Macro Model'''
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The micro model is somehow quite easy to understand. We can relatively directly observe and analyze the location and state of each cell, so that this model is suitable for small-scale colony pattern vicissitude analysis. However the application of several random factors like division probability or others eventually complicates the anticipation process. Moreover, variations exist every time of simulation. We have to observe the shape of colony directly(with eyes) on a larger scale, which would obey the statistical rules. For the sake of seeking the most probable situation, we have a macro model to simulate. Macro model differs from the micro model mainly in that the number of cells in a spatial unit no longer limits to one but pertains to another characteristic: cellular density. The macro model would on one hand reduce the quantity of calculation and on the other hand reflects the possible results more realisticly.
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Compared to micro model, the AHL density u(r, t) for every spatial unit possesses the same meaning and remain compliant to equation(4). Whereas, the characteristic of cells is no longer weighed by whether existed or not, nor does  the type or state of a single cell be considered, but using the density of green normal cells  and that  of red special cells
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'''The Cellular Density Logistic Model'''
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In the micro model, we can discuss the division process and growing period of single cells, but not in the macro model any more. For the concept of single cells is eliminated and instead we just take into consideration the quantity of cells in certain areas which would obey some kinds of rules. Here, we applied the classic Logistic Model to lineate the quantity visisitude of colony. With the original number of cells ranging from 1 and 200 and a environmental limit of 100, the changing situation of the number of cells is shown as below:
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[[File:Seuologist.GIF|center]]
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*Logistic model with initial cell number of 1 and 200
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Revision as of 14:28, 25 September 2012

header1
header2



Modeling






Simulation

  • Introduction
  • Light Induce
  • Auto-differentiation

Data Process

  • Parameter Estimates
  • Image Process

System Simulation


Introduction

In order to verify the availability and probable effect of our design scheme, simulation mathematical models based on Cellular Automata technique have been conducted.

In catering to our past experiment scheme, we have constructed two models as follows:

  • Light Sensing Model: use light to trigger the asymmetry process of the colony;
  • Movement Model: use more complicated pathways to induce the break of symmetry.

A cellular automaton is in nature a finite-state machine in discrete time as well as space studied in computability theory,mathematics, physics, complexity science, theoretical biology and microstructure modeling.

This model provides a significant reference to the appraise of realistic experiments by simulating the whole pattern changing process, which consists of division, movement, death and some relevant ones.

Light Induced Model


Micro Model

To display the simulation results directly, we have constructed a micro model based on cellular automata. Each minimum spatial unit is able to hold up at most one cell, which can be characterized by a cellular automaton; Meanwhile, another property that wonders in every minimum spatial unit is the density of AHL, which relies on the density diffusion equation. The detailed cellular automata rules would be as follows.


a) Cell types

Each minimum spatial unit in this cellular automata model is able to hold up at most one cell. Cells can be divided into two types, normal cells(marked by green) and special cells(marked by red). Red cells are transferred from green cells by the trigger of light. The type of cells is denoted by ‘C’ as follows:

‘n’ represents the n th period, ‘(i, j)’ represents the location of the cell. Same below Red cells emit AHL at the rate of ‘q’ in every period.


b) Cell Division and Cellular States

Both kinds of cells are likely to divide. A mature cell possesses a division probability of Pdiv every time unit and gets two green cells after division. The newly generated cell would grow closely to the original cell and would emerge at the eight neighboring positions with equal probability. If the eight neighboring positions had been occupied, then the original cell would not be able to divide.

Consider the realistic condition where continuous cell division is impossible, so we use Φ to denote cellular states. At the very beginning Φ=1; Then with the cells growing, Φ=Φ+1 with every period; When Φ=τ, the cell would be mature enough to divide with a division probability of Pdiv during every period; After every division, the Φ(n;i,j) of the original and new cells would both change into:

However, in our system, as a signal molecule, AHL can trigger the antisense Ftsz part which can be functional as a division repressor. So Pdiv is actually a constant but a parameter proportional to the density of AHL. With several steps of calculations and experiments, the relationship between Pdiv and the density of AHL can be induced as follows:

Among it both ‘a’ and ‘b’ are unknown parameters.


c) Cell Movement

In the light sensing model, due to the big influence of light from the outer environment, cell movement has almost nothing to do with final results both in simulation or realistic experiments. As a result, we simplify the movement of cells. However, the movement of cells would no longer be negligible in the afterwards models. Further details on its rules and results to come afterwards.


d) Cell Death

In all models mentioned in this text, cell death has merely minor influence on our final results so it is neglected in all.


AHL Density Equation

AHL density can be expressed as u(r,t). Take the discrete characteristic of cellular automata into consideration, just denote it as . As a solute, AHL has the phenomenon of diffusion and decomposition. At mentioned above, red cells would spread out AHL. In conclusion, AHL complies to diffusion equation:

  • u: AHL density; D: diffusion constant; q: AHL releasing rate of a single triggered cell; γ describes the decomposition process of AHL; m: total number of cells.


Simulation Procedure

At the very beginning, AHL density u(r, 0)=0 on the infinite plane. In order to eliminate the asymmetry in the results that might be caused by the asymmetry of the original state, there is only one green cell at first. Choose several separate cells manually to shed light on. With the sliding improvement of the colony from merely one cell, green cells would eventually reach the light area where they would transform into red cells. Red cells begin to release AHL. When the quantity of red cells accumulates to a certain threshold, high density of AHL in certain areas would repress the division of cells and begin to trigger the differentiation of cell and therefore break the symmetry of the colony.


Results





Macro Model


The micro model is somehow quite easy to understand. We can relatively directly observe and analyze the location and state of each cell, so that this model is suitable for small-scale colony pattern vicissitude analysis. However the application of several random factors like division probability or others eventually complicates the anticipation process. Moreover, variations exist every time of simulation. We have to observe the shape of colony directly(with eyes) on a larger scale, which would obey the statistical rules. For the sake of seeking the most probable situation, we have a macro model to simulate. Macro model differs from the micro model mainly in that the number of cells in a spatial unit no longer limits to one but pertains to another characteristic: cellular density. The macro model would on one hand reduce the quantity of calculation and on the other hand reflects the possible results more realisticly.

Compared to micro model, the AHL density u(r, t) for every spatial unit possesses the same meaning and remain compliant to equation(4). Whereas, the characteristic of cells is no longer weighed by whether existed or not, nor does the type or state of a single cell be considered, but using the density of green normal cells and that of red special cells


The Cellular Density Logistic Model

In the micro model, we can discuss the division process and growing period of single cells, but not in the macro model any more. For the concept of single cells is eliminated and instead we just take into consideration the quantity of cells in certain areas which would obey some kinds of rules. Here, we applied the classic Logistic Model to lineate the quantity visisitude of colony. With the original number of cells ranging from 1 and 200 and a environmental limit of 100, the changing situation of the number of cells is shown as below:

  • Logistic model with initial cell number of 1 and 200




Division Inhibition