Team:Paris/Modeling/f4

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(Difference between revisions)
 
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{{Paris/Header|Method & Algorithm : ƒ4}}
{{Paris/Header|Method & Algorithm : ƒ4}}
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<center> = act_''pFliA'' </center>
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<br>
[[Image:f4DCA.png|thumb|Specific Plasmid Characterisation for &#131;4]]
[[Image:f4DCA.png|thumb|Specific Plasmid Characterisation for &#131;4]]
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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,
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>
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we have ''' [''FlhDC'']<sub>''real''</sub> = {coef<sub>''flhDC''</sub>} &#131;1([aTc]<sub>i</sub>) '''
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and <span style="color:#0000FF;">[''FliA'']<sub>''real''</sub> = {coef<sub>''fliA''</sub>} &#131;2([arab]<sub>i</sub>)</span>
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and ''' [''FliA'']<sub>''real''</sub> = {coef<sub>''fliA''</sub>} &#131;2([arab]<sub>i</sub>) '''
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but we use <span style="color:#0000FF;">[aTc]<sub>i</sub> = Inv_&#131;1( [''FlhDC''] ) </span>
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but we use ''' [aTc]<sub>i</sub> = Inv_&#131;1( [''FlhDC''] ) '''
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and        <span style="color:#0000FF;">[arab]<sub>i</sub> = Inv_&#131;2( [''FliA''] ) </span>
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and        ''' [arab]<sub>i</sub> = Inv_&#131;2( [''FliA''] ) '''
So, at steady-states,
So, at steady-states,

Latest revision as of 02:07, 30 October 2008

Method & Algorithm : ƒ4


= act_pFliA


Specific Plasmid Characterisation for ƒ4

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,

F4.jpg

we use this analytical expression to determine the parameters :

↓ Table of Values ↑


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.
ƒ4 activity of
pFliA with RBS E0032
nM.min-1



param signification
corresponding parameters in the equations
unit value comments
β18 total transcription rate of
FlhDC><pFliA with RBS E0032
β18
nM.min-1
(K1/{coefflhDC}) activation constant of FlhDC><pFliA
K1
nM
n1 complexation order of FlhDC><pFliA
n1
no dimension
β23 total transcription rate of
FliA><pFliA with RBS E0032
β23
nM.min-1
(K7/{coeffliA}) activation constant of FliA><pFliA
K7
nM
n10 complexation order of FliA><pFliA
n7
no dimension
↓ Algorithm ↑


find_ƒ4

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

SumpFliA.jpg


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