Team:ETH Zurich/modeling/qs

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(Difference between revisions)
(Chemical Species)
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* ΦC31: serine integrase that can fold into two conformations- ΦC31a and ΦC31b. We chose to use a common connotation for both conformations - ΦC31.
* ΦC31: serine integrase that can fold into two conformations- ΦC31a and ΦC31b. We chose to use a common connotation for both conformations - ΦC31.
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=== Modelization of DNA-binding sites ===
 
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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:
 
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* SI<sub>IntegraseName</sub>: inactive DNA binding site. No dimer is bound to this site, which has never been flipped.
 
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* SA<sub>IntegraseName</sub>: active DNA binding site. A dimer is to this site.
 
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* SF<sub>IntegraseName</sub>: flipped DNA binding site. This DNA binding site has been used by a flipping.
 
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[[File:ETH_Zurich_Integrases_sites.png|center|800px|thumb|The three different states of DBxb1-DNA binding sites.]]
 
=== Reactions ===
=== Reactions ===
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;For Bxb1:
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;For the Lux system:
$$ \begin{align}
$$ \begin{align}
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Bxb1 + Bxb1 &\leftrightarrow DBxb1 \\
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&\rightarrow LuxR \\
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DBxb1 + SI_{Bxb1} & \leftrightarrow SA_{Bxb1}\\
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Lux-AHL+LuxR & \leftrightarrow RLux\\
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Bxb1 &\rightarrow \\
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RLux}+RLux & \leftrightarrow DRLux\\
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DBxb1 &\rightarrow
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DRLux}+P_{luxOFF} & \leftrightarrow P_{luxON}\\
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P_{luxON}&\rightarrow P_{luxON}+mRNA_{Bxb1}\\
 +
mRNA_{Bxb1}&\rightarrow Bxb1\\
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AHL &\rightarrow \\
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LuxR &\rightarrow  \\
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R_{Lux} &\rightarrow\\
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DR_{Lux} &\rightarrow\\
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mRNA_{Bxb1} &\rightarrow\\
 +
Bxb1 &\rightarrow
\end{align}$$
\end{align}$$

Revision as of 16:34, 11 October 2014

iGEM ETH Zurich 2014