Team:Paris/Modeling/BOB

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{{Paris/Menu}}
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{{:Team:Paris/MenuBackup}}
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<center><html><div style="color:#275D96; font-size:2em;">BOB (Based On Bibliography) Approach</div></html></center>
 
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<center><html><div style="color:#275D96; font-size:2em;">BOB (Based On Bibliography) Approach</div></html></center>
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<br>
[[Image:Bob_marley.jpg|450px|thumb]]
[[Image:Bob_marley.jpg|450px|thumb]]
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** YFP behind pFlgA = f(FlhDC,FliA)
** YFP behind pFlgA = f(FlhDC,FliA)
** RFP and LasI behind pFlhB = f(FlhDC,FliA)
** RFP and LasI behind pFlhB = f(FlhDC,FliA)
-
(See also our [[Team:Paris/Project/FIFO|FIFO module]])
+
(See also our [[Team:Paris/Project/FIFO|FIFO module]] and the [[Team:Paris/Modeling/BOB/Simulations#FIFO|Simulation of the FIFO]])
* Second Subsystem[[Image:Subsystem2.jpg|center]]
* Second Subsystem[[Image:Subsystem2.jpg|center]]
** HSL = f(LasI) or f(LuxI) depending on which system is being used
** HSL = f(LasI) or f(LuxI) depending on which system is being used
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=== Mathematical model ===
=== Mathematical model ===
-
* Classically we use the following equation to model gene interactions :  
+
* Classically we use the following equation to model gene interactions (see for example in [[Team:Paris/Modeling/BOB#Bibliography|[5]]]) :  
<br>
<br>
[[Image:Classical_equation.jpg|center]]
[[Image:Classical_equation.jpg|center]]
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<br>
<br>
<br>
<br>
-
* Yet, the flagella gene network has been thoroughly studied in [1]. We used two major results presented in this study. Firstly, Shiraz Kalir and Uri Alon came up with the fact that the promoters of class 2 genes, among which fliL, flgA and flhB, behaved like SUM-gate functions with flhDC and fliA inputs. Secondly, their experiments proved that these influences could be considered as linear. Thus the following model:
+
* Yet, the flagella gene network has been thoroughly studied in [[Team:Paris/Modeling/BOB#Bibliography|[1]]]. We used two major results presented in this study. Firstly, Shiraz Kalir and Uri Alon came up with the fact that the promoters of class 2 genes, among which fliL, flgA and flhB, behaved like SUM-gate functions with flhDC and fliA inputs. Secondly, their experiments proved that these influences could be considered as linear. Thus the following model:
<br>
<br>
[[Image:Promoter_Activity.jpg|center]]
[[Image:Promoter_Activity.jpg|center]]
Line 83: Line 85:
=== Discussion ===
=== Discussion ===
==== Normalization ====
==== Normalization ====
-
*First of all, we wanted to have a proper time scale. We the set the degradation rates, γ ,to 1. It is important to note that this degradation rate is represent the influence of the degradation and dilution. We assume that the degradation can be neglected compared to the dilution caused by the cell growth. Then we have:
+
*First of all, we wanted to have a proper time scale. We the set the degradation rates, γ ,to 1. It is important to note that this degradation rate represents the influence of the degradation and dilution. We assume that the degradation can be neglected compared to the dilution caused by the cell growth. Then we have:
<br>
<br>
[[Image:Gamma_Expression.jpg|center]]
[[Image:Gamma_Expression.jpg|center]]
Line 110: Line 112:
==== Which gene goes were? ====
==== Which gene goes were? ====
-
* The key element to understand is that fliA stands as an accelerator. The first influence is caused by flhDC, and fliA gives the last burst. fliA also has a great influence in the fading phase, since it introduces a delay (result found by experiments in [1]). This is what determined our choice in the order of fliL, flgA and flhB. We wanted to put in first the gene that was the least influenced by fliA, and in the end the gene the most influenced by fliA.  
+
* The key element to understand is that fliA stands as an accelerator. The first influence is caused by flhDC, and fliA gives the last burst. fliA also has a great influence in the fading phase, since it introduces a delay (result found by experiments in [[Team:Paris/Modeling/BOB#Bibliography|[1]]]). This is what determined our choice in the order of fliL, flgA and flhB. We wanted to put in first the gene that was the least influenced by fliA, and in the end the gene the most influenced by fliA.  
<br>
<br>
[[Image:Graph_No_FliA_2.jpg|center]]
[[Image:Graph_No_FliA_2.jpg|center]]
[[Image:Graph_FliA.jpg|center]]
[[Image:Graph_FliA.jpg|center]]
-
 
+
* We wished to run simulations with Matlab to confirm this reasoning : for further information see our [[Team:Paris/Modeling/BOB/Simulations#FIFO|simulations]].
-
=== Justification of this linear choice ===
+
* In fact, this enabled us to force the curves into crossing themselves. In addition, the delay imposed by fliA in the decreasing phase, would permit us to widen the delays between the first and the last gene expression, thus getting better conditions to observe the FIFO in the wet lab.
-
akaike...
+
-
<br>
+
== Second Subsystem ==
== Second Subsystem ==
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==== Dynamics of HSL ====
==== Dynamics of HSL ====
* First and foremost, it is clear that HSL is the key element in the synchronisation process: we used a diffusive specie in order to insert a reference specie inside the medium. Therefore, the HSL concentration, denoted [HSL], is the link to the outside medium HSL concentration, denoted [HSL<sub>ext</sub>], which is the intermediate reference value.
* First and foremost, it is clear that HSL is the key element in the synchronisation process: we used a diffusive specie in order to insert a reference specie inside the medium. Therefore, the HSL concentration, denoted [HSL], is the link to the outside medium HSL concentration, denoted [HSL<sub>ext</sub>], which is the intermediate reference value.
-
* We use the classical osmosis term '''η x ( [HSL] - [HSL<sub>ext</sub>] )''' where '''η = membrane permeability x ( area<sub> 1cell</sub> / volume<sub> 1cell</sub> )''' is the diffusion rate expressed in time<sup>-1</sup>.
+
* We use the classical osmosis term '''η x ( [HSL] - [HSL<sub>ext</sub>] )''' where '''η = membrane permeability x ( Surface<sub> 1cell</sub> / Volume<sub> 1cell</sub> )''' is the diffusion rate expressed in time<sup>-1</sup>.
* The degradation rate is naturally linear: '''- γ x [HSL]'''.
* The degradation rate is naturally linear: '''- γ x [HSL]'''.
-
* To model the production, we were at first inspired by [2] where it is described as being linear: '''β x [LasI]''' where β is a given constant value. However, the results presented in this study were introduced as only being theoretical so we chose to model the creation of HSL by a Michaelis Menten expression (because there is no known cooperativity).
+
* To model the production, we were inspired by [[Team:Paris/Modeling/BOB#Bibliography|[2]]] where it is described as being linear: '''β x [LasI]''' (β is a given constant value). However, the results presented in this study were introduced as only being theoretical and it is also possible to model the creation of HSL by a Michaelis Menten expression (similar to a Hill expression when there is no cooperativity).
* The final expression where Θ<sub>HSL</sub> is expressed in concentration units and β<sub>HSL</sub> in (concentration * time) unit is: [[Image:HSL_final_choice_2.jpg|center]]
* The final expression where Θ<sub>HSL</sub> is expressed in concentration units and β<sub>HSL</sub> in (concentration * time) unit is: [[Image:HSL_final_choice_2.jpg|center]]
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* The evolution of HSLext may be described with three terms. First of all, there is a dilution rate, D<sub>renewal</sub>, due to the renewal of the chemostat. There is the usual degradation rate,γ<sub>[HSL]<sub>ext</sub></sub>. Then we have a the osmotic term, likewise the one presented before :  
* The evolution of HSLext may be described with three terms. First of all, there is a dilution rate, D<sub>renewal</sub>, due to the renewal of the chemostat. There is the usual degradation rate,γ<sub>[HSL]<sub>ext</sub></sub>. Then we have a the osmotic term, likewise the one presented before :  
** If [HSL]<sub>ext</sub> > [HSL], then there is a positive flow of HSL from inside the cells to the exterior medium.  
** If [HSL]<sub>ext</sub> > [HSL], then there is a positive flow of HSL from inside the cells to the exterior medium.  
-
** Else, if[HSL]<sub>ext</sub> > [HSL], then there is a negative of HSL (from outside to inside the cells).  
+
** Else, if[HSL]<sub>ext</sub> < [HSL], then there is a negative flow of HSL (from outside to inside the cells).  
[[Image:HSLext_sum_2.jpg|center]]
[[Image:HSLext_sum_2.jpg|center]]
Which gives
Which gives
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==== TetR=f(HSL) ====
==== TetR=f(HSL) ====
-
* Here we had the choice to model the complexation phase of HSL and lasR, and then the binding phase of this complex on the pLas promoter. We assumed that those stages were short, and then decided to model them by a single step.
+
* Here we had the choice to model the complexation phase of HSL and lasR, and then the binding phase of this complex on the pLas promoter. We assumed that those stages were fast, and then decided to model them by a single step.
-
* We checked in the registry that the pLas sequence was the same as in [promoter specificity]. It is explained that there are two operators, denoted OP1 and OP2. The Hill parameters were detailed in this article, hence our modeling choice :
+
* We checked in the registry that the pLas sequence was the same as the one of lasB described in [[Team:Paris/Modeling/BOB#Bibliography|[4]]]. It is explained that there are two operators, denoted OP1 and OP2. The Hill parameters were detailed in this article, hence our modeling choice:
[[Image:tetR_final_2.jpg|center]]
[[Image:tetR_final_2.jpg|center]]
-
* It is noticeable that we assumed a 'sum' behavior for the two operons.
+
* It is noticeable that we assumed a "sum" behavior for the two operons.
=== Discussion ===
=== Discussion ===
==== Normalization ====
==== Normalization ====
-
* In this subsystem, we decided not to normalize the HSL concentration, since HSL<sub>ext</sub> is to be understood as a global variable.
+
* [HSL] can be normalized for simplification purposes. According to [[Team:Paris/Modeling/BOB#Bibliography|[8]]] (table 2 of the article), at the equilibrium [HSL] can be estimated to be about 230 nM. Thresholds for TetR production (hill kinetics depending on [HSL]) become 0.160 nM -> 6.96e-4 and 0.0089 nM -> 3.87e-5 (initial values are from [[Team:Paris/Modeling/BOB#Bibliography|[4]]] and the reference value from [[Team:Paris/Modeling/BOB#Bibliography|[8]]] then becomes the 1 = 'equilibrium' value)
* Nevertheless, it is coherent to normalize [tetR]. Likewise we set out time-scale by setting the degradation rates to the value of 1 in the previous equations, we set γ<sub>tetR</sub> to 1. Following the same train of thought as in the first subsystem, if we consider the equilibrium hypothetical stage when [HSL] concentration is fully expressed, we deduce that :  
* Nevertheless, it is coherent to normalize [tetR]. Likewise we set out time-scale by setting the degradation rates to the value of 1 in the previous equations, we set γ<sub>tetR</sub> to 1. Following the same train of thought as in the first subsystem, if we consider the equilibrium hypothetical stage when [HSL] concentration is fully expressed, we deduce that :  
[[Image:Beta_limit_2.jpg|center]]
[[Image:Beta_limit_2.jpg|center]]
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[[Image:Beta_Tet_2.jpg|center]]
[[Image:Beta_Tet_2.jpg|center]]
-
==== For the Lux system ====
+
==== Concerning the Lux system ====
-
[[Image:lux_system.jpg|center]]
+
[[Image:lux_system_2.jpg|center]]
-
* We shall try to construct both systems (las and lux). In the case of the lux system, the only change would be in the expression of TetR
+
* We shall try to construct both systems (las and lux). In the case of the lux system, the only change would be in the expression of TetR. Indeed, since there is a single operator we have modeled [TetR] dynamics as follows, reasoning like in the las system :
 +
 
 +
[[Image:TetR_lux.jpg|center]]
 +
 
 +
* Concerning the normalization, according to the previous reasoning, we have β<sub>TetR(lux)</sub>=1.
 +
 
 +
==== Simplification ====
 +
In our system, HSL activates the pLas promoter which control the transcription of tetR. According to the bibliography the pLas promoter is made of two distincts operators, each operator's action being modeled by a Hill function as explained above.
 +
 
 +
However, to simplify the global model, we wanted to keep only linear or hill activation but not mixed expressions like a sum of two hill functions. Any function can be approximated by another but the square difference will of course become important if you don't choose the new function and its parameters accurately.
 +
 
 +
To sum up, we had to simplify '''β<sub>TetR</sub> x ( hill(x , θ<sub>TetR-OP1</sub> , n<sub>TetR-OP1</sub>) + hill(x , θ<sub>TetR-OP2</sub> , n<sub>TetR-OP2</sub>) )''' by something more consistant with the model. We chose to use a single hill function '''0.5 x β<sub>TetR</sub> x hill(x,θ<sub>TetR-s</sub>,n<sub>TetR-s</sub>)''', still having to find the new threshold and steepness parameters (subscripted <sub>-s</sub>).
 +
 
 +
It is an optimization issue which can be solved by the '''lsqnonlin''' Matlab function.
 +
The following function that we wrote can find the parameters of the hill function that fit the best to a given timespan and set of points:
 +
 
 +
<html><pre>
 +
<span class="keyword">function</span> <span class="string">optimal_parameters</span> <span class="string">=</span> <span class="string">hill_find(xspan,set)</span>
 +
 +
<span class="keyword">function</span> output = difference(xspan,parameters)
 +
output = parameters(1) * arrayfun(@(x)(hill(x,parameters(2),parameters(3))),xspan) - set;
 +
<span class="keyword">end</span>
 +
lsqnonlin_options = optimset(<span class="string">'LevenbergMarquardt'</span>,<span class="string">'on'</span>,<span class="string">'TolX'</span>,1e-10,<span class="string">'MaxFunEvals'</span>,1e7,<span class="string">'TolFun'</span>,1e-5);
 +
optimal_parameters = lsqnonlin(@(parameters)difference(xspan,parameters), ...
 +
[1 1 1],[0 0 0],[10 10 10],lsqnonlin_options);
 +
optimal_parameters = optimal_parameters(:);
 +
 +
<span class="keyword">end</span>
 +
</pre></html>
 +
 
 +
The script below then use this hill_find function and the optimal_parameters it returns:
 +
 
 +
<html><pre>
 +
close, clear <span class="string">all</span>
 +
 +
xspan = linspace(0,1,1e4);
 +
hillsum = 0.5 * arrayfun(@(x)(hill(x,6.96e-4,1) + hill(x,3.87e-5,1.5)),xspan);
 +
parameters = hill_find(xspan,hillsum);
 +
newhill = parameters(1)*arrayfun(@(x)(hill(x,parameters(2),parameters(3))),xspan);
 +
 +
plot(xspan,hillsum,<span class="string">'blue'</span>)
 +
hold <span class="string">on</span>
 +
plot(xspan,newhill,<span class="string">'red'</span>)
 +
</pre></html>
 +
 
 +
[[Image:hillsum2hill.jpg|center]]
 +
 
 +
We were, by running this script, able to compare the original function with a single hill. As you can see on the screenshot above, the difference is tiny so the approximation should not modify the dynamic behaviour of the global system. Values obtained are: '''β<sub>TetR</sub>=1.9948''', '''θ<sub>TetR-s</sub>=0.3638''' and '''n<sub>TetR-s</sub>=0.0145'''. Note that it does not have a true "meaning" but it is only a good numerical approximation to simplify 2 functions into one on the [0 1] domain.
 +
 
 +
[[Image:TetR_simplif.jpg|center]]
== Third Subsystem ==
== Third Subsystem ==
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=== Discussion : Normalization ===
=== Discussion : Normalization ===
-
* Likewise the previous analysis, we set γ<sub>lflhDC</sub> to 1. Then, since FlhDC is fully expressed when TetR is not, we see that when solving under this conditions, we get
+
* Likewise the previous analysis, we set γ<sub>FlhDC</sub> to 1. Then, since FlhDC is fully expressed when TetR is not, we see that when solving under this conditions, we get
[[Image:flhDC_norm.jpg|center]]
[[Image:flhDC_norm.jpg|center]]
hence the need to set
hence the need to set
[[Image:Beta_flhDC.jpg|center]]
[[Image:Beta_flhDC.jpg|center]]
 +
* Furthermore, since [TetR] has been normalized, we have to do so for θ<sub>FlhDC</sub> as well, since its role is to stand as a reference concentration for [TetR]. Therefore, we have to normalize it in the same way we did for [TetR]:
 +
we had [[Image:norm_tetR.jpg|center]]
 +
which means we have to impose : [[Image:norm_Theta.jpg|center]]
== Parameters summary ==
== Parameters summary ==
=== Parameters Table ===
=== Parameters Table ===
-
(Under Construction)
 
-
 
<center>
<center>
{|
{|
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| Unit
| Unit
| Source
| Source
 +
|- style="background: #dddddd;"   
|- style="background: #dddddd;"   
-
| style="background: #D4E2EF;" | α<sub>cell</sub>
+
| style="background: #D4E2EF;"|γ
|  
|  
-
| Growth rate
+
| Degradation rate
-
|
+
-
|
+
-
| min<sup>-1</sup>
+
-
| [[Team:Paris/Modeling/BOB#Remarks|wet-lab]]
+
-
|- style="background: #dddddd;" 
+
-
| style="background: #D4E2EF;"| c<sub>max</sub>
+
-
|
+
-
| Carrying capacity for cell growth
+
-
| 100000
+
-
| 100000
+
-
| cells/nL
+
-
| [[Team:Paris/Modeling/BOB#Remarks|[3]]]
+
-
|- style="background: #dddddd;" 
+
-
| style="background: #D4E2EF;"| D<sub>renewal</sub>
+
-
|
+
-
| Dilution rate
+
-
| (0.005)
+
-
| (0.005)
+
-
| min<sup>-1</sup>
+
-
| [[Team:Paris/Modeling/BOB#Remarks|wet-lab]] ([[Team:Paris/Modeling/BOB#Bibliography|[3]]])
+
-
|- style="background: #dddddd;" 
+
-
| style="background: #D4E2EF;"| d
+
-
|
+
-
| Death rate
+
| 0.0198
| 0.0198
| 1
| 1
| min<sup>-1</sup>
| min<sup>-1</sup>
| [[Team:Paris/Modeling/BOB#Remarks|wet-lab]]
| [[Team:Paris/Modeling/BOB#Remarks|wet-lab]]
-
|- style="background: #dddddd;"
+
|- style="background: #dddddd;"
-
| style="background: #D4E2EF;"|γ<sub>FliA</sub>
+
| style="background: #D4E2EF;" |β<sub>FlhDC</sub>
|  
|  
-
| Degradation rate
+
| Maximum production rate
-
| 0.0198
+
|
| 1
| 1
| min<sup>-1</sup>
| min<sup>-1</sup>
-
| [[Team:Paris/Modeling/BOB#Remarks|wet-lab]]
+
| [[Team:Paris/Modeling/BOB#Remarks|]]
|- style="background: #dddddd;"
|- style="background: #dddddd;"
| style="background: #D4E2EF;"|β<sub>FliA</sub>
| style="background: #D4E2EF;"|β<sub>FliA</sub>
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| min<sup>-1</sup>
| min<sup>-1</sup>
| [[Team:Paris/Modeling/BOB#Bibliography|[1]]]
| [[Team:Paris/Modeling/BOB#Bibliography|[1]]]
-
|- style="background: #dddddd;"
 
-
| style="background: #D4E2EF;"|γ<sub>CFP</sub>
 
-
|
 
-
| Degradation rate
 
-
| 0.0198
 
-
| 1
 
-
| min<sup>-1</sup>
 
-
| [[Team:Paris/Modeling/BOB#Remarks|wet-lab]]
 
|- style="background: #dddddd;"
|- style="background: #dddddd;"
| style="background: #D4E2EF;"|β<sub>CFP</sub>
| style="background: #D4E2EF;"|β<sub>CFP</sub>
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| min<sup>-1</sup>
| min<sup>-1</sup>
| [[Team:Paris/Modeling/BOB#Bibliography|[1]]]
| [[Team:Paris/Modeling/BOB#Bibliography|[1]]]
-
|- style="background: #dddddd;"
 
-
| style="background: #D4E2EF;"|γ<sub>YFP</sub>
 
-
|
 
-
| Degradation rate
 
-
| 0.0198
 
-
| 1
 
-
| min<sup>-1</sup>
 
-
| [[Team:Paris/Modeling/BOB#Remarks|wet-lab]]
 
|- style="background: #dddddd;"
|- style="background: #dddddd;"
| style="background: #D4E2EF;" |β<sub>YFP</sub>
| style="background: #D4E2EF;" |β<sub>YFP</sub>
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| min<sup>-1</sup>
| min<sup>-1</sup>
| [[Team:Paris/Modeling/BOB#Bibliography|[1]]]
| [[Team:Paris/Modeling/BOB#Bibliography|[1]]]
-
|- style="background: #dddddd;"
 
-
| style="background: #D4E2EF;" |γ<sub>RFP</sub>
 
-
|
 
-
| Degradation rate
 
-
| 0.0198
 
-
| 1
 
-
| min<sup>-1</sup>
 
-
| [[Team:Paris/Modeling/BOB#Remarks|wet-lab]]
 
|- style="background: #dddddd;"
|- style="background: #dddddd;"
| style="background: #D4E2EF;" |β<sub>RFP</sub>
| style="background: #D4E2EF;" |β<sub>RFP</sub>
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| [[Team:Paris/Modeling/BOB#Bibliography|[1]]]
| [[Team:Paris/Modeling/BOB#Bibliography|[1]]]
|- style="background: #dddddd;"
|- style="background: #dddddd;"
-
| style="background: #D4E2EF;" |γ<sub>HSL</sub>  
+
| style="background: #D4E2EF;" |n<sub>envZ</sub>
|  
|  
-
| Degradation rate
+
| Hill coefficient
-
| 0.0198
+
-
| 1
+
-
| min<sup>-1</sup>
+
-
| [[Team:Paris/Modeling/BOB#Remarks|wet-lab]]
+
-
|- style="background: #dddddd;"
+
-
| style="background: #D4E2EF;" |β<sub>HSL</sub>
+
|  
|  
-
| Production rate
+
| 4
-
| 0.01
+
| ¤
-
| 0.01
+
| [[Team:Paris/Modeling/BOB#Bibliography|]]
-
| min<sup>-1</sup>
+
-
| [[Team:Paris/Modeling/BOB#Bibliography|[2]]]
+
|- style="background: #dddddd;"
|- style="background: #dddddd;"
-
| style="background: #D4E2EF;" |θ<sub>HSL</sub>  
+
| style="background: #D4E2EF;" |θ<sub>envZ</sub>
|  
|  
| Hill characteristic concentration
| Hill characteristic concentration
|  
|  
-
|
+
| 0.5
-
|  
+
| [[Team:Paris/Modeling/BOB#Remarks|c.u]]
-
|
+
| [[Team:Paris/Modeling/BOB#Bibliography|∅]]
|- style="background: #dddddd;"
|- style="background: #dddddd;"
-
| style="background: #D4E2EF;" |η
+
| style="background: #D4E2EF;" |β<sub>envZ</sub>
-
|
+
-
| Diffusion rate
+
-
| 2
+
-
|
+
|  
|  
-
| [[Team:Paris/Modeling/BOB#Bibliography|[2]]]
+
| Maximum production rate
-
|- style="background: #dddddd;"
+
-
| style="background: #D4E2EF;"|γ<sub>HSL<sub>ext</sub></sub> <br> <br>
+
-
|
+
-
| Degradation rate
+
|  
|  
 +
| 1
 +
| min<sup>-1</sup>
 +
| [[Team:Paris/Modeling/BOB#Remarks|∅]]
 +
|- style="background: #dddddd;" 
 +
| style="background: #D4E2EF;" | α<sub>cell</sub>
|  
|  
 +
| Growth rate
 +
| 0.0198
 +
| 1
 +
| min<sup>-1</sup>
 +
| [[Team:Paris/Modeling/BOB#Remarks|wet-lab]]
 +
|- style="background: #dddddd;" 
 +
| style="background: #D4E2EF;"| c<sub>max</sub>
|
|
 +
| Carrying capacity for cell growth
 +
| 0.1
 +
| 0.1
 +
| µm<sup>3</sup>
 +
| [[Team:Paris/Modeling/BOB#Bibliography|[3]]]
 +
|- style="background: #dddddd;" 
 +
| style="background: #D4E2EF;"| D<sub>renewal</sub>
|
|
-
|- style="background: #dddddd;"
+
| Dilution rate
-
| style="background: #D4E2EF;"|V<sub>1Cell</sub>
+
| 0.00198
-
|
+
| 0.1
-
| Cell Volume
+
| min<sup>-1</sup>
-
|
+
| [[Team:Paris/Modeling/BOB#Remarks|wet-lab]] ([[Team:Paris/Modeling/BOB#Bibliography|[3]]])
-
|
+
|- style="background: #dddddd;"
-
|
+
| style="background: #D4E2EF;"| d
|
|
 +
| Death rate
 +
| 0.0099
 +
| 0.5
 +
| min<sup>-1</sup>
 +
| [[Team:Paris/Modeling/BOB#Remarks|wet-lab]]
|- style="background: #dddddd;"
|- style="background: #dddddd;"
-
| style="background: #D4E2EF;"|V<sub>tot</sub>
+
| style="background: #D4E2EF;" |γ<sub>HSL</sub>  
-
|
+
-
| Total Volume
+
-
|
+
-
|
+
-
|
+
-
|
+
-
|- style="background: #dddddd;"
+
-
| style="background: #D4E2EF;" |γ<sub>tetR</sub>
+
|  
|  
| Degradation rate
| Degradation rate
-
| 0.0198
+
| 0.0053
-
| 1
+
| 0.2690
| min<sup>-1</sup>
| min<sup>-1</sup>
| [[Team:Paris/Modeling/BOB#Remarks|wet-lab]]
| [[Team:Paris/Modeling/BOB#Remarks|wet-lab]]
|- style="background: #dddddd;"
|- style="background: #dddddd;"
-
| style="background: #D4E2EF;" |β<sub>tetR</sub>
+
| style="background: #D4E2EF;"|γ<sub>HSL<sub>ext</sub></sub> <br> <br>
|  
|  
-
| Maximum production rate for the first operator
+
| Degradation rate
-
| 110
+
| 0.0106
-
| 0.5
+
| 0.5380
-
|min<sup>-1</sup>
+
| min<sup>-1</sup>
-
| [[Team:Paris/Modeling/BOB#Bibliography|[4]]]
+
| [[Team:Paris/Modeling/BOB#Bibliography|[6]]]
|- style="background: #dddddd;"
|- style="background: #dddddd;"
-
| style="background: #D4E2EF;" |n<sub>tetR-OP1</sub>
+
| style="background: #D4E2EF;" |β<sub>HSL</sub>  
|  
|  
-
| Hill coefficient for the first operator
+
| Production rate
-
| 1.0
+
| 0.3168
-
| 1.0
+
| 16
-
|  
+
| min<sup>-1</sup>
-
| [[Team:Paris/Modeling/BOB#Bibliography|[4]]]
+
| [[Team:Paris/Modeling/BOB#Bibliography|]]
|- style="background: #dddddd;"
|- style="background: #dddddd;"
-
| style="background: #D4E2EF;" |θ<sub>tetR-OP1</sub>
+
| style="background: #D4E2EF;" |η
-
|  
+
|
-
| Hill characteristic concentration for the first operator
+
| Diffusion rate
-
| 160
+
| 10
-
| 160
+
| 505
-
|  
+
| min<sup>-1</sup>
-
| [[Team:Paris/Modeling/BOB#Bibliography|[4]]]
+
| [[Team:Paris/Modeling/BOB#Bibliography|[2]]]
|- style="background: #dddddd;"
|- style="background: #dddddd;"
-
| style="background: #D4E2EF;" |n<sub>tetR-OP2</sub>
+
| style="background: #D4E2EF;"|V<sub>1Cell</sub>
|  
|  
-
| Hill coefficient for the second operator
+
| Cell Volume
-
| 1.5
+
-
| 1.5
+
-
|
+
-
| [[Team:Paris/Modeling/BOB#Bibliography|[4]]]
+
-
|- style="background: #dddddd;"
+
-
| style="background: #D4E2EF;" |θ<sub>tetR-OP2</sub>
+
-
|
+
-
| Hill characteristic concentration for the second operator
+
-
| 8.9
+
-
| 8.9
+
-
|
+
-
| [[Team:Paris/Modeling/BOB#Bibliography|[4]]]
+
-
|- style="background: #dddddd;"
+
-
| style="background: #D4E2EF;" |γ<sub>flhDC</sub>
+
-
|
+
-
| Degradation rate
+
-
| 0.0198
+
| 1
| 1
-
| min<sup>-1</sup>
+
| 1
 +
| µm<sup>3</sup>
| [[Team:Paris/Modeling/BOB#Remarks|wet-lab]]
| [[Team:Paris/Modeling/BOB#Remarks|wet-lab]]
|- style="background: #dddddd;"
|- style="background: #dddddd;"
-
| style="background: #D4E2EF;" |β<sub>FlhDC</sub>
+
| style="background: #D4E2EF;" |n<sub>HSL</sub>
-
|
+
-
| Maximum production rate
+
-
| ∅
+
-
| 1
+
-
| min<sup>-1</sup>
+
-
| [[Team:Paris/Modeling/BOB#Remarks|∅]]
+
-
|- style="background: #dddddd;"
+
-
| style="background: #D4E2EF;" |n<sub>FlhDC</sub>
+
|  
|  
| Hill coefficient
| Hill coefficient
|  
|  
-
|
+
| 4
-
|  
+
| ¤
-
|
+
| [[Team:Paris/Modeling/BOB#Bibliography|[3]]]
|- style="background: #dddddd;"
|- style="background: #dddddd;"
-
| style="background: #D4E2EF;" |θ<sub>FlhDC</sub>
+
| style="background: #D4E2EF;" |θ<sub>HSL</sub>
|  
|  
-
| Hill characteristic concentration
+
| Hill characteristic concentration for the second operator
|  
|  
-
|
+
| 0.5
-
|  
+
| [[Team:Paris/Modeling/BOB#Remarks|c.u]]
-
|
+
| [[Team:Paris/Modeling/BOB#Bibliography|[3]]]
 +
 
 +
 
|}</center>
|}</center>
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The value for half-life time we found and used is 35min.
The value for half-life time we found and used is 35min.
-
* Furthermore, D<sub>renewal</sub> is a wet-lab data since we can impose the exact value of our wish. What is more, thatnks to this model, we are able to evaluate an optimisez value of this parameter so as to carry the experiments with the best probability to have the wanted behavior.
+
* Furthermore, D<sub>renewal</sub> is a wet-lab data since we can impose the exact value of our wish. What is more, thanks to this model, we are able to evaluate an optimised value of this parameter so as to carry the experiments with the best probability to have the wanted behavior.
* ∅ occurance in the table corresponds to value we did not need due to our normalization process.
* ∅ occurance in the table corresponds to value we did not need due to our normalization process.
Line 480: Line 461:
Much of our inspiration comes from four articles to which we shall refer in the next subsections :  
Much of our inspiration comes from four articles to which we shall refer in the next subsections :  
<br>
<br>
-
* [1] Shiraz Kalir, Uri Alon. Using quantitative blueprint to reprogram the dynamics of the flagella network. Cell, June 11, 2004, Vol.117, 713-720.
+
* [1] Shiraz Kalir, Uri Alon. ''Using quantitative blueprint to reprogram the dynamics of the flagella network.'' Cell, June 11, 2004, Vol.117, 713-720.
-
* [2]Jordi Garcia-Ojalvo, Michael B. Elowitz, Steven H. Strogratz. Modeling a synthetic multicellular clock : repressilators coupled by quorum sensing. PNAS, July 27, 2004, Vol. 101, no. 30.
+
* [2]Jordi Garcia-Ojalvo, Michael B. Elowitz, Steven H. Strogratz. ''Modeling a synthetic multicellular clock : repressilators coupled by quorum sensing.'' PNAS, July 27, 2004, Vol. 101, no. 30.
-
* [3]Frederick K. Balagaddé, Hao Song, Jun Ozaki, Cynthia H. Collins, Matthew Barnet, Frances H. Arnold, Stephen R. Quake, Lingchong You. A Synthetic Escherichia Coli predator prey ecosystem. Molecular Systems Biology. 2008.
+
* [3]Frederick K. Balagaddé, Hao Song, Jun Ozaki, Cynthia H. Collins, Matthew Barnet, Frances H. Arnold, Stephen R. Quake, Lingchong You. ''A Synthetic Escherichia Coli predator prey ecosystem.'' Molecular Systems Biology. 2008.
-
* [4]M. Schuster, M. L Urbanowski, E. P. Greenberg. Promoter Specificity in Pseudomonas aeruginosa quorum sensing revealed by DNA binding of purified LasR. PNAS, November 9, 2004, vol. 101, no. 45.
+
* [4]M. Schuster, M. L Urbanowski, E. P. Greenberg. ''Promoter Specificity in Pseudomonas aeruginosa quorum sensing revealed by DNA binding of purified LasR.'' PNAS, November 9, 2004, vol. 101, no. 45.
-
 
+
* [5]Nitzan Rosenfeld, Michael B. Elowitz, Uri Alon. ''Negative autoregulation speeds the response times of transcription networks.'' JMB, 2003, 323, 785-793.
-
A VOIR
+
* [6]Lingchong You, Robert Sidney Cox III, Ron Weiss, Frances H. Arnold. ''Programmed population control by cell-cell communication and regulation killing.'' Nature, April 22, 2004.
-
 
+
* [7] Braun D et al. ''Parameter Estimation for Two Synthetic Gene Networks: A Case Study'', ICASSP 5:769-772, 2005.
-
 
+
* [8] Pearson et al. ''Active Efflux and Diffusion Are Involved in Transport of Pseudomonas aeruginosa Cell-to-Cell Signals'' Journal of Bacteriology, February 1999, p. 1203-1210, Vol. 181, No. 4
-
 
+
-
* [3]Nitzan Rosenfeld, Uri Alon. Response delays and the structure of transcription networks. JMB, 2003, 329, 645-654.
+
-
* [4]Nitzan Rosenfeld, Michael B. Elowitz, Uri Alon. Negative autoregulation speeds the response times of transcription networks. JMB, 2003, 323, 785-793.
+
-
* [5]S.Kalir, J. McClure, K. Pabbaraju, C. Southward, M. Ronen, S. Leibler, M. G. Surette, U. Alon. Ordering genes in a flagella pathway by analysis of expression kinetics from living bacteria. Science, June 2001, Vol 292.
+
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Latest revision as of 04:46, 30 October 2008

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BOB (Based On Bibliography) Approach


Bob marley.jpg

Contents

Introduction

  • The key problem with a dynamic system consists in the fact that adding a new equation gives a more detailed idea of the overall process, but one looses meaning by doing so since new undefined parameters appear. Hence, it becomes hard to link those parameters with a biological meaning and reality.
  • In that respect we chose to build at first a simplified model, which would enable us to help us understand the processes implied in the system. In that respect, we chose not to introduce the mRNA state between transcription and translation in our model. We presented things as if a protein would act directly upon the following. Furthermore, we assumed that describing routinely every step, would only force us into finding more parameters.
  • This preliminary approach is mainly based on a bibliographical work. In fact, it is important to understand that with this approach, we did not intend to design the most accurate model possible. We found essential to choose only parameters that we could determine or control in the wet lab. The main goal was to get quickly a first idea of the way our system could behave.
  • The goal here is to present the differential equations we used in the model. At each step we shall describe why we chose these precise equations, the drawbacks and possible improvements, the parameters involved and eventually a biologically coherent value.

Model

  • Here is an overall view of the whole system :
Globalmodel.jpg

Steps of the Model

We chose to broke up this system in three sub systems for presentation clarity

  • Population Growth : we wished to model the population evolution in the chemostat, since our experiments will be carried out in these conditions.
  • First Subsystem
    Subsystem1.jpg
    • FliA behind pFliA= f(FlhDC,FliA)
    • CFP behind pFliL = f(FlhDC,FliA)
    • YFP behind pFlgA = f(FlhDC,FliA)
    • RFP and LasI behind pFlhB = f(FlhDC,FliA)

(See also our FIFO module and the Simulation of the FIFO)

  • Second Subsystem
    Subsystem2.jpg
    • HSL = f(LasI) or f(LuxI) depending on which system is being used
    • HSL ⇋ HSLext
    • TetR = f(HSL)

(See also our Synchronisation module)

  • Third Subsystem
    Subsystem3.jpg
    • FlhDC = f(TetR)
  • In each subsystem we will describe the way we decided to normalize each protein resulting from genic expression. In fact, in every case we normalize the concentration by their maximum values, in order to keep the influence relations that rule the system behavior. This will enable us to compare the different concentration evolutions, and interpret the data we get from our simulations.

Population evolution

  • First of all, it seems important at this stage to present the way we interpret the evolution of the population in the chemostat. We want to impose to our model the fact that the rate of production has to be proportional to the existing population and to the amount of available resources. Hence a logistic model of the population, where c denotes the concentration of cells in the medium:


Population evolution 2.jpg


  • Then, we need to add the death term, and a dilution term cause by the renewal of the chemostat. Finally we get :


Population evolution full 2.jpg


where cmax is the carrying capacity for cell growth, and D renewal.jpg the dilution rate, d the death rate constant

First Subsystem

Steps involved

  • FliA behind pFliA= f(FlhDC,FliA)
  • CFP behind pFliL = f(FlhDC,FliA)
  • YFP behind pFlgA = f(FlhDC,FliA)
  • RFP and LasI behind pFlhB = f(FlhDC,FliA)

Mathematical model

  • Classically we use the following equation to model gene interactions (see for example in [5]) :


Classical equation.jpg


where [Y] denotes the concentration of Y protein and γ its degradation rate (which unit is time-1).

  • Yet, the flagella gene network has been thoroughly studied in [1]. We used two major results presented in this study. Firstly, Shiraz Kalir and Uri Alon came up with the fact that the promoters of class 2 genes, among which fliL, flgA and flhB, behaved like SUM-gate functions with flhDC and fliA inputs. Secondly, their experiments proved that these influences could be considered as linear. Thus the following model:


Promoter Activity.jpg


β and β’ represent the relative influence of flhDC and fliA respectively, the units of β and β’ being time-1.

  • Furthermore, they came up with numerical values of β and β’ for each gene, which fitted quite well to their experiments. We then decided that we could use those values as well in our model.



  • Finally, here are our final equations:


FliA dynamics.jpg
CFP.jpg
YFP.jpg
RFP.jpg


Discussion

Normalization

  • First of all, we wanted to have a proper time scale. We the set the degradation rates, γ ,to 1. It is important to note that this degradation rate represents the influence of the degradation and dilution. We assume that the degradation can be neglected compared to the dilution caused by the cell growth. Then we have:


Gamma Expression.jpg


  • Since we can know easily the value of the real half-time, we may know the real timescale out of our computations. We kept the designation “degradation rate” for convenience, so as not to mix up with the dilution that occurs with the HSL in the synchronisation step.
  • We kept the β and β’ values found by S. Kalir and U. Alon, since they showed the relative influence of flhDC and fliA. To have the same order of magnitude between each specie, we normalized those parameters between 0 and 1 as following. We reasoned independently for each equation, wishing to set the equilibrium values of the concentration to 1 given input values of 1. This gave:
Beta Resize.jpg


Beta p Resize.jpg


  • In fact, if we take CFP for example:
CFP.jpg

The maximum of [CFP] is reached when [fliA] = 1 and [flhDC] = 1 ; when we solve with these condidtions, we obtain :

CFP Solve.jpg

Then setting the equilibrium value of [CFP] to 1 corresponds to setting

Beta Gamma resize.jpg
  • The analysis of fliA is different, but not the result:
FliA Analysis.jpg

With an input of flhDC equal to 1, the solution of the differential equation is:

FliA Solve.jpg

And the condition on the equilibrium imposes

Beta Gamma Resize FliA.jpg
  • To conclude, we see that we always get the same condition:
Final Resize.jpg
  • Finally, since we had imposed γ=1 we resulted with β+β'=1.

Which gene goes were?

  • The key element to understand is that fliA stands as an accelerator. The first influence is caused by flhDC, and fliA gives the last burst. fliA also has a great influence in the fading phase, since it introduces a delay (result found by experiments in [1]). This is what determined our choice in the order of fliL, flgA and flhB. We wanted to put in first the gene that was the least influenced by fliA, and in the end the gene the most influenced by fliA.


Graph No FliA 2.jpg
Graph FliA.jpg
  • We wished to run simulations with Matlab to confirm this reasoning : for further information see our simulations.
  • In fact, this enabled us to force the curves into crossing themselves. In addition, the delay imposed by fliA in the decreasing phase, would permit us to widen the delays between the first and the last gene expression, thus getting better conditions to observe the FIFO in the wet lab.

Second Subsystem

Steps involved

  • HSL = f(LasI) or f(LuxI) depending on which system is being used
  • HSL ⇋ HSLext
  • TetR = f(HSL)

Mathematical Model

Dynamics of HSL

  • First and foremost, it is clear that HSL is the key element in the synchronisation process: we used a diffusive specie in order to insert a reference specie inside the medium. Therefore, the HSL concentration, denoted [HSL], is the link to the outside medium HSL concentration, denoted [HSLext], which is the intermediate reference value.
  • We use the classical osmosis term η x ( [HSL] - [HSLext] ) where η = membrane permeability x ( Surface 1cell / Volume 1cell ) is the diffusion rate expressed in time-1.
  • The degradation rate is naturally linear: - γ x [HSL].
  • To model the production, we were inspired by [2] where it is described as being linear: β x [LasI] (β is a given constant value). However, the results presented in this study were introduced as only being theoretical and it is also possible to model the creation of HSL by a Michaelis Menten expression (similar to a Hill expression when there is no cooperativity).
  • The final expression where ΘHSL is expressed in concentration units and βHSL in (concentration * time) unit is:
    HSL final choice 2.jpg
  • It is important to note that we took into account the fact that lasR/(lasR linked to HSL) was a function of HSL. However, we assumed that the fraction of HSL bound to lasR would not influence HSL concentration; this is the reason why, no "degradation due to binding" term appears in the HSL model.
  • Last but not least, lasR does not intervene in the equations because we have considered it to be constitutively expressed. Like aTc (see below), it can be used later as a control for our system.

Dynamics of HSLext

  • The evolution of HSLext may be described with three terms. First of all, there is a dilution rate, Drenewal, due to the renewal of the chemostat. There is the usual degradation rate,γ[HSL]ext. Then we have a the osmotic term, likewise the one presented before :
    • If [HSL]ext > [HSL], then there is a positive flow of HSL from inside the cells to the exterior medium.
    • Else, if[HSL]ext < [HSL], then there is a negative flow of HSL (from outside to inside the cells).
HSLext sum 2.jpg

Which gives

HSLext final 2.jpg

where

Cell number volume.jpg

TetR=f(HSL)

  • Here we had the choice to model the complexation phase of HSL and lasR, and then the binding phase of this complex on the pLas promoter. We assumed that those stages were fast, and then decided to model them by a single step.
  • We checked in the registry that the pLas sequence was the same as the one of lasB described in [4]. It is explained that there are two operators, denoted OP1 and OP2. The Hill parameters were detailed in this article, hence our modeling choice:
TetR final 2.jpg
  • It is noticeable that we assumed a "sum" behavior for the two operons.

Discussion

Normalization

  • [HSL] can be normalized for simplification purposes. According to [8] (table 2 of the article), at the equilibrium [HSL] can be estimated to be about 230 nM. Thresholds for TetR production (hill kinetics depending on [HSL]) become 0.160 nM -> 6.96e-4 and 0.0089 nM -> 3.87e-5 (initial values are from [4] and the reference value from [8] then becomes the 1 = 'equilibrium' value)
  • Nevertheless, it is coherent to normalize [tetR]. Likewise we set out time-scale by setting the degradation rates to the value of 1 in the previous equations, we set γtetR to 1. Following the same train of thought as in the first subsystem, if we consider the equilibrium hypothetical stage when [HSL] concentration is fully expressed, we deduce that :
Beta limit 2.jpg

and solving gives:

TetR solve 2.jpg

thus the conclusion :

Beta Tet 2.jpg

Concerning the Lux system

Lux system 2.jpg
  • We shall try to construct both systems (las and lux). In the case of the lux system, the only change would be in the expression of TetR. Indeed, since there is a single operator we have modeled [TetR] dynamics as follows, reasoning like in the las system :
TetR lux.jpg
  • Concerning the normalization, according to the previous reasoning, we have βTetR(lux)=1.

Simplification

In our system, HSL activates the pLas promoter which control the transcription of tetR. According to the bibliography the pLas promoter is made of two distincts operators, each operator's action being modeled by a Hill function as explained above.

However, to simplify the global model, we wanted to keep only linear or hill activation but not mixed expressions like a sum of two hill functions. Any function can be approximated by another but the square difference will of course become important if you don't choose the new function and its parameters accurately.

To sum up, we had to simplify βTetR x ( hill(x , θTetR-OP1 , nTetR-OP1) + hill(x , θTetR-OP2 , nTetR-OP2) ) by something more consistant with the model. We chose to use a single hill function 0.5 x βTetR x hill(x,θTetR-s,nTetR-s), still having to find the new threshold and steepness parameters (subscripted -s).

It is an optimization issue which can be solved by the lsqnonlin Matlab function. The following function that we wrote can find the parameters of the hill function that fit the best to a given timespan and set of points:

function optimal_parameters = hill_find(xspan,set) 
 
function output = difference(xspan,parameters)
output = parameters(1) * arrayfun(@(x)(hill(x,parameters(2),parameters(3))),xspan) - set;
end 
lsqnonlin_options = optimset('LevenbergMarquardt','on','TolX',1e-10,'MaxFunEvals',1e7,'TolFun',1e-5);
optimal_parameters = lsqnonlin(@(parameters)difference(xspan,parameters), ...
[1 1 1],[0 0 0],[10 10 10],lsqnonlin_options);
optimal_parameters = optimal_parameters(:);
 
end 

The script below then use this hill_find function and the optimal_parameters it returns:

close, clear all 
 
xspan = linspace(0,1,1e4);
hillsum = 0.5 * arrayfun(@(x)(hill(x,6.96e-4,1) + hill(x,3.87e-5,1.5)),xspan);
parameters = hill_find(xspan,hillsum);
newhill = parameters(1)*arrayfun(@(x)(hill(x,parameters(2),parameters(3))),xspan);
 
plot(xspan,hillsum,'blue')
hold on 
plot(xspan,newhill,'red')

Hillsum2hill.jpg

We were, by running this script, able to compare the original function with a single hill. As you can see on the screenshot above, the difference is tiny so the approximation should not modify the dynamic behaviour of the global system. Values obtained are: βTetR=1.9948, θTetR-s=0.3638 and nTetR-s=0.0145. Note that it does not have a true "meaning" but it is only a good numerical approximation to simplify 2 functions into one on the [0 1] domain.

TetR simplif.jpg

Third Subsystem

Mathematical Model

  • FlhDC = f(TetR)
  • Here we chose to understand aTc as a regulation and control variable, that will help us influence our parameters in the wet lab. Therefore, [aTc] does not appear in this model.
  • For this last step, in addition to the usual degradation term, we simply chose a complete Hill function to describe the dynamics of flhDC, because this is the way it is commonly described in the literature:
FlhDC dynamics final.jpg

Discussion : Normalization

  • Likewise the previous analysis, we set γFlhDC to 1. Then, since FlhDC is fully expressed when TetR is not, we see that when solving under this conditions, we get
FlhDC norm.jpg

hence the need to set

Beta flhDC.jpg
  • Furthermore, since [TetR] has been normalized, we have to do so for θFlhDC as well, since its role is to stand as a reference concentration for [TetR]. Therefore, we have to normalize it in the same way we did for [TetR]:
we had
Norm tetR.jpg
which means we have to impose :
Norm Theta.jpg

Parameters summary

Parameters Table

Parameter Table
Parameter Parameter in code Meaning Original Value Normalized Value Unit Source


γ Degradation rate 0.0198 1 min-1 wet-lab
βFlhDC Maximum production rate 1 min-1
βFliA FlhDC activation coefficient 50 0.1429 min-1 [1]
β'FliA FliA activation coefficient 300 0.8571 min-1 [1]
βCFP FlhDC activation coefficient 1200 0.8276 min-1 [1]
β'CFP FliA activation coefficient 250 0.1724 min-1 [1]
βYFP FlhDC activation coefficient 150 0.3333 min-1 [1]
β'YFP FliA activation coefficient 300 0.6667 min-1 [1]
βRFP FlhDC activation coefficient 100 0.2222 min-1 [1]
β'RFP FliA activation coefficient 350 0.7778 min-1 [1]
nenvZ Hill coefficient 4 ¤
θenvZ Hill characteristic concentration 0.5 c.u
βenvZ Maximum production rate 1 min-1
αcell Growth rate 0.0198 1 min-1 wet-lab
cmax Carrying capacity for cell growth 0.1 0.1 µm3 [3]
Drenewal Dilution rate 0.00198 0.1 min-1 wet-lab ([3])
d Death rate 0.0099 0.5 min-1 wet-lab
γHSL Degradation rate 0.0053 0.2690 min-1 wet-lab
γHSLext

Degradation rate 0.0106 0.5380 min-1 [6]
βHSL Production rate 0.3168 16 min-1
η Diffusion rate 10 505 min-1 [2]
V1Cell Cell Volume 1 1 µm3 wet-lab
nHSL Hill coefficient 4 ¤ [3]
θHSL Hill characteristic concentration for the second operator 0.5 c.u [3]


Remarks

  • We denote by c.u the arbitrary (due to normalization) concentration unit.
  • We evaluated in the wet lab the half life time for our cells, and then calculated the degradation constants using :
Gamma Expression.jpg

The value for half-life time we found and used is 35min.

  • Furthermore, Drenewal is a wet-lab data since we can impose the exact value of our wish. What is more, thanks to this model, we are able to evaluate an optimised value of this parameter so as to carry the experiments with the best probability to have the wanted behavior.
  • ∅ occurance in the table corresponds to value we did not need due to our normalization process.

Bibliography

Much of our inspiration comes from four articles to which we shall refer in the next subsections :

  • [1] Shiraz Kalir, Uri Alon. Using quantitative blueprint to reprogram the dynamics of the flagella network. Cell, June 11, 2004, Vol.117, 713-720.
  • [2]Jordi Garcia-Ojalvo, Michael B. Elowitz, Steven H. Strogratz. Modeling a synthetic multicellular clock : repressilators coupled by quorum sensing. PNAS, July 27, 2004, Vol. 101, no. 30.
  • [3]Frederick K. Balagaddé, Hao Song, Jun Ozaki, Cynthia H. Collins, Matthew Barnet, Frances H. Arnold, Stephen R. Quake, Lingchong You. A Synthetic Escherichia Coli predator prey ecosystem. Molecular Systems Biology. 2008.
  • [4]M. Schuster, M. L Urbanowski, E. P. Greenberg. Promoter Specificity in Pseudomonas aeruginosa quorum sensing revealed by DNA binding of purified LasR. PNAS, November 9, 2004, vol. 101, no. 45.
  • [5]Nitzan Rosenfeld, Michael B. Elowitz, Uri Alon. Negative autoregulation speeds the response times of transcription networks. JMB, 2003, 323, 785-793.
  • [6]Lingchong You, Robert Sidney Cox III, Ron Weiss, Frances H. Arnold. Programmed population control by cell-cell communication and regulation killing. Nature, April 22, 2004.
  • [7] Braun D et al. Parameter Estimation for Two Synthetic Gene Networks: A Case Study, ICASSP 5:769-772, 2005.
  • [8] Pearson et al. Active Efflux and Diffusion Are Involved in Transport of Pseudomonas aeruginosa Cell-to-Cell Signals Journal of Bacteriology, February 1999, p. 1203-1210, Vol. 181, No. 4
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