Team:KULeuven/Model/Cell Death

From 2008.igem.org

(Difference between revisions)
(Parameters)
(Parameters)
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| [http://jb.asm.org/cgi/content/full/189/11/4127?view=long&pmid=17400743 link]
| [http://jb.asm.org/cgi/content/full/189/11/4127?view=long&pmid=17400743 link]
|-
|-
-
| K<sub>LuxR</sub>
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| K<sub>HSL_LuxR</sub>
-
| 1E-9 [M]/L
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| 4.05E-6 [M]/L
-
| binding LuxR on LuxPromotor
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| binding HSL_LuxR on LuxPromotor
-
| [http://jb.asm.org/cgi/content/full/189/11/4127?view=long&pmid=17400743 link]
+
| [http://parts.mit.edu/igem07/index.php/Tokyo/AHL_assay link]
|-
|-
! colspan="4" style="border-bottom: 1px solid #003E81;" | Hill Cooperativity
! colspan="4" style="border-bottom: 1px solid #003E81;" | Hill Cooperativity
|-
|-
-
| n<sub>LuxR</sub>
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| n<sub>HSL_LuxR</sub>
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| 2.0
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| 2.08
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|
+
|  
|  
 +
| [http://parts.mit.edu/igem07/index.php/Tokyo/AHL_assay link]
|-
|-
! colspan="4" style="border-bottom: 1px solid #003E81;" | Transcription Rates
! colspan="4" style="border-bottom: 1px solid #003E81;" | Transcription Rates

Revision as of 11:32, 28 July 2008

Result:

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Contents

Cell Death

Position in the system

The Cell Death subsystem receives input from two other subsystems, namely:

LuxR is the component repressing the regulation of CcdB, the toxic product causing cell death. There the LuxR production is constitutive, no protein controls the gene regulation of LuxR, but the amount of LuxR available to repress the transcripion of the CcdB gene is controlled by HSL (Homoserine lactone).

If the inverter subsystem produces HSL (occurs when no light is detectable), this will forms a complex with LuxR. This will diminish the amount of LuxR available to repress the CcdB transcription and initiate cell death. When waiting long enough the amount of HSL becomes critical.

If however the pulse generator becomes active (by the filter), it will produce a pulse of lactonase, which will then bind to the HSL, reacting to an hydroxy-acid. As opposed to HSL, this hydroxy-acid will no longer form a complex with LuxR. This increase in LuxR lowers the CcdB production. The challenge is to generate a pulse of lactonase high enough to neutralise all HSL present in the cell.

Describing the system

Cell Death.jpg

ODE's

Parameters

Parameter values (Cell Death)
Name Value Comments Reference
Degradation Rates
dLuxR 0.0010 s-1
dLuxR_HSL 0.0010 s-1 complex of HSL and LuxR degrades, giving back HSL
dRNA_LuxR 0.00227 s-1 link
dCcdB 7.7E-5 s-1 link
dRNA_CcdB 0.00231 s-1 link
dHSL 1.02E-6 s-1 link
Association/Dissociation/Reaction Rates
kass (HSL+LuxR) 1E6 s-1 association rate of HSL with LuxR. Chosen to be relatively (to the other rate constants) high and such that Kdiss (HSL + LuxR) equals 10-6
kdiss (HSL+LuxR) 1 s-1 dissociation rate of the HSL-LuxR complex
kass (HSL+lactonase) 1E6 s-1 association rate of HSL with lactonase
kdiss (HSL+lactonase) 446.5 s-1 dissociation rate of the HSL-lactonase complex
kcat (HSL:hydroxy-acid) 29 s-1 catalytic transformation of HSL to an hydroxy-acid, lactonase is the enzyme link
Dissociation Constants
KHSL_LuxR 1E-6 [M]/L kdiss / kass (HSL+LuxR) link
KHSL_LuxR 4.05E-6 [M]/L binding HSL_LuxR on LuxPromotor link
Hill Cooperativity
nHSL_LuxR 2.08 link
Transcription Rates
kmRNA_LuxR (constitutive promotor) 0.025 s-1 see Constitutive Promotors & E. coli transcription Rates
kmRNA_CcdB 0.025 s-1 maximal transcription rate for CcdB RNA (no LuxR repressor present)

Models

CellDesigner (SBML file)

Cell Death
Cell Death
Cell Death

Matlab