Team:ETH Zurich/modeling/qs
From 2014.igem.org
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* Lux-AHL: | * Lux-AHL: | ||
- | * LuxR: | + | * LuxR: constitutively expressed regulator protein that can bind Lux-AHL and stimulate transcription of Bxb1. |
* DBxb1: | * DBxb1: | ||
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* Las-AHL: | * Las-AHL: | ||
- | * LasR: | + | * LasR: constitutively expressed regulator protein that can bind Las-AHL and stimulate transcription of ΦC31. |
* RLas: | * RLas: | ||
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* DRLas: | * DRLas: | ||
- | * ΦC31 | + | * ΦC31: |
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Revision as of 16:02, 11 October 2014
Modeling quorum sensing
Model
The Quorum sensing module is mainly involved in receiving signals from the sender cells. The sender cells secrete some signalling molecules (inducers) which bind to the regulator molecules in the receiver cells, thus activating the transcription of certain genes. The model for this module is presented below.
Chemical Species
- Lux-AHL:
- LuxR: constitutively expressed regulator protein that can bind Lux-AHL and stimulate transcription of Bxb1.
- DBxb1:
- RLux:
- DRLux:
- Bxb1:
- Las-AHL:
- LasR: constitutively expressed regulator protein that can bind Las-AHL and stimulate transcription of ΦC31.
- RLas:
- DRLas:
- ΦC31:
Modelization of DNA-binding sites
Each dimer of integrases can specifically bind to a DNA binding site. As the flipping is irreversible, these DNA binding sites can be three possible states:
- SIIntegraseName: inactive DNA binding site. No dimer is bound to this site, which has never been flipped.
- SAIntegraseName: active DNA binding site. A dimer is to this site.
- SFIntegraseName: flipped DNA binding site. This DNA binding site has been used by a flipping.
Reactions
- For Bxb1
$$ \begin{align} Bxb1 + Bxb1 &\leftrightarrow DBxb1 \\ DBxb1 + SI_{Bxb1} & \leftrightarrow SA_{Bxb1}\\ Bxb1 &\rightarrow \\ DBxb1 &\rightarrow \end{align}$$
- For ΦC31
\begin{align} \phi C31 + \phi C31 &\leftrightarrow D\phi C 31 \\ D\phi C 31 + SI_{\phi C31} & \leftrightarrow SA_{\phi C31}\\ \phi C31 &\rightarrow \\ D\phi C31 &\rightarrow \end{align}
Differential Equations
Applying mass action kinetic laws, we obtain the following set of differential equations.
$$\frac{d[Bxb1]}{dt}=-2 k_{dimBxb1}[Bxb1]^2+ 2 k_{-dimBxb1}[DBxb1]-d_{Bxb1}[Bxb1]$$
$$\frac{d[DBxb1]}{dt}=-k_{DNABxb1}[DBxb1][SI_{Bxb1}]+k_{-DNABxb1}[SA_{Bxb1}]+k_{dimBxb1}[Bxb1]^2-k_{-dimBxb1}[DBxb1a]-d_{DBxb1}[DBxb1]$$
$$\frac{d[SA_{Bxb1}]}{dt}=k_{DNABxb1}[DBxb1][SI_{Bxb1}]-k_{-DNABxb1}[SA_{Bxb1}]$$
Characterization
Data
Assumptions
Parameter fitting
Range of validity of the assumptions
Characterization
Data
Assumptions
Parameter fitting
Range of validity of the assumptions