Team:Paris/Modeling/f7

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[[Image:f7DCA.png|thumb|Specific Plasmid Characterisation for ƒ7]]
[[Image:f7DCA.png|thumb|Specific Plasmid Characterisation for ƒ7]]
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We have <span style="color:#0000FF;">[''FlhDC'']<sub>''real''</sub> = {coef<sub>''flhDC''</sub>} &#131;1([aTc]<sub>i</sub>)</span>
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According to the characterization plasmid (see right) and to our modeling, in the '''exponential phase of growth''', at the steady state,
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we have <span style="color:#0000FF;">[''FlhDC'']<sub>''real''</sub> = {coef<sub>''flhDC''</sub>} &#131;1([aTc]<sub>i</sub>)</span>
and <span style="color:#0000FF;">[''FliA'']<sub>''real''</sub> = {coef<sub>''fliA''</sub>} &#131;2([arab]<sub>i</sub>)</span>
and <span style="color:#0000FF;">[''FliA'']<sub>''real''</sub> = {coef<sub>''fliA''</sub>} &#131;2([arab]<sub>i</sub>)</span>
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[[Image:F7a.jpg|center]]
[[Image:F7a.jpg|center]]
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<br>
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we use this analytical expression to determine the parameters :
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{{Paris/Toggle|Table|Team:Paris/Modeling/More_f7_Table}}  
{{Paris/Toggle|Table|Team:Paris/Modeling/More_f7_Table}}  
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Revision as of 01:59, 30 October 2008

Method & Algorithm : ƒ7


Specific Plasmid Characterisation for ƒ7

According to the characterization plasmid (see right) and to our modeling, in the exponential phase of growth, at the steady state,

we have [FlhDC]real = {coefflhDC} ƒ1([aTc]i) and [FliA]real = {coeffliA} ƒ2([arab]i)

but we use [aTc]i = Inv_ƒ1( [FlhDC] ) and [arab]i = Inv_ƒ2( [FliA] )

So, at steady-states,

F7a.jpg

we use this analytical expression to determine the parameters :

↓ Table ↑


param signification unit value comments
(fluorescence) value of the observed fluorescence au need for 20 mesures with well choosen values of [aTc]i
and for 20 mesures with well choosen values of [arab]i
and 5x5 measures for the relation below?
conversion conversion ratio between
fluorescence and concentration
↓ gives ↓ 		nM.au-1 (1/79.429)
[GFP] GFP concentration at steady-state nM
γGFP dilution-degradation rate
of GFP(mut3b)
↓ gives ↓ 		min-1 0.0198 Time Cell Division : 35 min.
ƒ7 activity of
pFlgB with RBS E0032 		nM.min-1



param signification
corresponding parameters in the equations 		unit value comments
β28 total transcription rate of
FlhDC><pFlgB with RBS E0032
β28 		nM.min-1
(K4/{coeffliA}) activation constant of FlhDC><pFlgB
K4 		nM
n4 complexation order of FlhDC><pFlgB
n4 		no dimension
β29 total transcription rate of
FlhDC><pFlgB with RBS E0032
β29 		nM.min-1
(K10/{coefflhDC}) activation constant of FlhDC><pFlgB
K10 		nM
n10 complexation order of FlhDC><pFlgB
n10 		no dimension
↓ Algorithm ↑


find_ƒP 

function optimal_parameters = find_FP(X_data, Y_data, initial_parameters)
% gives the 'best parameters' involved in f4, f5, f6, f7 or f8  
% with FlhDC = 0 or FliA = 0 by least-square optimisation
 
% X_data = vector of given values of [FliA]i or [FlhDC]i (experimentally
% controled)
% Y_data = vector of experimentally measured values f4, f5, f6, f7 or f8
% corresponding of the X_data
% initial_parameters = values of the parameters proposed by the literature
%                       or simply guessed
%                    = [beta, K -> (K)/(coef), n]
 
     function output = act_pProm(parameters, X_data)
         for k = 1:length(X_data)
                 output(k) = parameters(1)*hill(X_data(k), parameters(2), parameters(3));
         end
     end
 
options=optimset('LevenbergMarquardt','on','TolX',1e-10,'MaxFunEvals',1e10,'TolFun',1e-10,'MaxIter',1e4);
% options for the function lsqcurvefit
 
optimal_parameters = lsqcurvefit( @(parameters, X_data) act_pProm(parameters, X_data),...
     initial_parameters, X_data, Y_data, options );
% search for the fittest parameters, between 1/10 and 10 times the initial
% parameters
 
end

Then, if we have time, we want to verify the expected relation

SumpFlgB.jpg


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<Back - to "Protocol Of Characterization" |

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