Team:KAIST-Korea/Project/Modeling

From 2010.igem.org

(Difference between revisions)
 
(5 intermediate revisions not shown)
Line 25: Line 25:
<img src = "https://static.igem.org/mediawiki/2010/b/bd/Modeling1.png" width = 400>
<img src = "https://static.igem.org/mediawiki/2010/b/bd/Modeling1.png" width = 400>
</html>
</html>
 +
<br>
<br>
<br>
&nbsp;&nbsp;And we can expect that the concentration of FGFRCDnP is constant at equilibrium state. The concentration of FGFRCDnP is<br>
&nbsp;&nbsp;And we can expect that the concentration of FGFRCDnP is constant at equilibrium state. The concentration of FGFRCDnP is<br>
Line 30: Line 31:
<img src = "https://static.igem.org/mediawiki/2010/a/a6/KAISTModeling2.png" width = 200>
<img src = "https://static.igem.org/mediawiki/2010/a/a6/KAISTModeling2.png" width = 200>
</html>
</html>
 +
<br>
<br>
<br>
&nbsp;&nbsp;And the concentration of FGFRCD is
&nbsp;&nbsp;And the concentration of FGFRCD is
<br>
<br>
<html>
<html>
-
<img src = "https://static.igem.org/mediawiki/2010/a/a6/KAISTModeling2.png" width = 200>
+
<img src = "https://static.igem.org/mediawiki/2010/5/5e/KAISTModeling3.png" width = 150>
</html>
</html>
 +
<br>
<br>
<br>
&nbsp;&nbsp;And the concentration of FGFRC is
&nbsp;&nbsp;And the concentration of FGFRC is
<br>
<br>
<html>
<html>
-
<img src = "https://static.igem.org/mediawiki/2010/a/a6/KAISTModeling2.png" width = 200>
+
<img src = "https://static.igem.org/mediawiki/2010/c/c0/KAISTModeling4.png" width = 200>
</html>
</html>
 +
<br>
<br>
<br>
&nbsp;&nbsp;Therefore, the concentration of FGFRCDnP as the function of concentration of FGFR [FGFR], that of antigen [antigen] and phosphorylation number n is<br>
&nbsp;&nbsp;Therefore, the concentration of FGFRCDnP as the function of concentration of FGFR [FGFR], that of antigen [antigen] and phosphorylation number n is<br>
<html>
<html>
-
<img src = "https://static.igem.org/mediawiki/2010/a/a6/KAISTModeling2.png" width = 200>
+
<img src = "https://static.igem.org/mediawiki/2010/0/02/KAISTModeling5.png" width = 500>
</html>
</html>
 +
<br>
<br>
<br>

Latest revision as of 05:22, 16 August 2010

 

Modeling



  Leaving cell transmit signal through chemical modifications of signal-related molecules like phosphorylation, methylation, acetylation or ubiquitination. And these chemical modifications are basically chemical reactions. Therefore, we can assume signal transduction pathway as sequential chemical reactions. We applied this assumption to signal transduction initiated by modified FGFR-antigen binding. Signal transduction follows these steps.

  1. Antigen binds to the single chain antibody of modified FGFR and form FGFR-complex(FGFRC).
  2. Two FGFR-complexes bind each other and form FGFR-complex-dimer(FGFRCD).
  3. FGFRCD phosphorylate each other and form FGFR-complex-dimer-phosphorylate (FGFRCDnP)
  4. FGFRCDnP phosphorylate STAT1 to for STAT1P.
  5. Two STAT1Ps bind each other and form STAT1P-dimer.
  6. STAT1P-dimer near cell surface diffuse to inside of nucleus of yeast.
  7. STAT1P-dimer in nucleus binds to GAS element and activate GFP gene.



  And these steps may be formulated as these reactions.


  And we can expect that the concentration of FGFRCDnP is constant at equilibrium state. The concentration of FGFRCDnP is


  And the concentration of FGFRCD is


  And the concentration of FGFRC is


  Therefore, the concentration of FGFRCDnP as the function of concentration of FGFR [FGFR], that of antigen [antigen] and phosphorylation number n is