ETHZ/Simulations

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Contents

Basic Model

Constitutively produced proteins

Model01.png

Learning system

Model02.png

Reporter system

Model03.png

System Equations

Constitutively produced proteins

Eq01.png

Learning system

Eq02.png

Reporter system

Eq03.png

Allosteric regulation

Eq04.png


Comments

Note that the three constitutively produced proteins R, S and L exist in two different forms: as free proteins and in complexes they build with IR, IS and IL, respectively. The total amount of protein is denoted with a subscript t (e.g. Rt) in the above formulas. The amount of protein existing as complex is denoted with a superscript * (e.g. R*). The difference is the amount of free protein (e.g. Rt - R*).

Model Parameters

Parameter Value Description Comments
aR basic production of lacI
aS basic production of tetR
aL basic production of luxR
aQ1 basic production of cI
aQ2 basic production of p22cII
aYFP basic production of YFP
aGFP basic production of GFP
aRFP basic production of RFP
aCFP basic production of CFP
dR 0.06 degradation of lacI Ref. [4] --please only add parameter values with proper dimensions,
a number like this is useless (Uhrm 04:43, 13 September 2007 (EDT))--
dS degradation of tetR
dL degradation of luxR
dQ1 degradation of cI
dQ2 degradation of p22cII
dYFP degradation of YFP
dGFP degradation of GFP
dRFP degradation of RFP
dCFP degradation of CFP
dIL degradation of AHL-luxR activator
dIR degradation of IPTG-lacI repressor
dIS degradation of aTc-tetR repressor
cQ1,1 promoter strength (R/Q2 inhibited) maybe Ref. [5] can be of help here (for inhibition of R)
cQ1,2 promoter strength (L activated/Q2 inhibited)
cQ2,1 promoter strength (S/Q1 inhibited) maybe Ref. [5] can be of help here (for inhibition of Q1)
cQ2,2 promoter strength (L activated/Q1 inhibited) maybe Ref. [5] can be of help here (for inhibition of Q1)
cYFP promoter strength (S/Q1 inhibited) see also cQ2,1
cGFP promoter strength (R/Q2 inhibited) see also cQ1,1
cRFP promoter strength (S/Q2 inhibited)
cCFP promoter strength (R/Q1 inhibited)
KR 1.3e-3 - 2e-3 [mM/h] lacI repressor dissociation constant lower value is from Ref. [2], higher value is from Ref. [5]
KIR 1.5e-10 [mM/h] IPTG-lacI repressor dissociation constant Ref. [5]
KS tetR repressor dissociation constant
KIS aTc-tetR repressor dissociation constant
KL luxR activator dissociation constant
KIL AHL-luxR activator dissociation constant
KQ1 2e-3 [mM/h] cI repressor dissociation constant Ref. [5]
KQ2 p22cII repressor dissociation constant
nR 1 lacI repressor Hill cooperativity Ref. [5]
nIR 2 IPTG-lacI repressor Hill cooperativity Ref. [5]
nS 3 tetR repressor Hill cooperativity Ref. [3]
nIS aTc-tetR repressor Hill cooperativity
nL 1 luxR activator Hill cooperativity Ref. [3]
nIL 1 AHL-luxR activator Hill cooperativity Ref. [3]
nQ1 1.9 cI repressor Hill cooperativity Ref. [5]
nQ2 p22cII repressor Hill cooperativity

References

  1. A synthetic time-delay circuit in mammalian cells and mice (http://www.pnas.org/cgi/content/abstract/104/8/2643)
  2. Detailed map of a cis-regulatory input function (http://www.pnas.org/cgi/content/full/100/13/7702?ck=nck)
  3. Parameter Estimation for two synthetic gene networks (http://ieeexplore.ieee.org/iel5/9711/30654/01416417.pdf)
  4. Supplementary on-line information for "A Synthetic gene-metabolic oscillator" (no link)
  5. Genetic network driven control of PHBV copolymer composition (http://doi:10.1016/j.jbiotec.2005.08.030)

Variable Mapping

Variable Compound
R lacI
IR IPTG
S tetR
IS aTc
L luxR
IL AHL
Q1 cI
Q2 p22cII