Timer Plus Sumo

From 2013.igem.org

(Difference between revisions)
Line 5: Line 5:
<html>
<html>
-
<div style="margin-top:10px;margin-left:50px;margin-right:50px;float:left;display:inline-block;">   
+
<div style="margin-top:10px;margin-left:30px;margin-right:30px;float:left;display:inline-block;">   
<h2 align="center">Timer Plus Sumo</h2>
<h2 align="center">Timer Plus Sumo</h2>
<br>
<br>
Line 18: Line 18:
</center>
</center>
-
<div style="margin-top:40px;margin-left:50px;margin-right:50px;float:left;display:inline-block;">   
+
<div style="margin-top:40px;margin-left:30px;margin-right:30px;float:left;display:inline-block;">   
<h2 align="center">Differential Equations</h2>
<h2 align="center">Differential Equations</h2>
Line 32: Line 32:
</center>
</center>
-
<div style="margin-top:30px;margin-left:50px;margin-right:50px;float:left;display:inline-block;">   
+
<div style="margin-top:30px;margin-left:30px;margin-right:30px;float:left;display:inline-block;">   
<h2 align="center">Parameters</h2>
<h2 align="center">Parameters</h2>
<br>
<br>
Line 51: Line 51:
The promoter strengths of cI and Tet are taken as a factor of T7. PcI is found to be approximatly
The promoter strengths of cI and Tet are taken as a factor of T7. PcI is found to be approximatly
0.43 times the strength of T7 [1] and Ptet is approximatly 2.79. [2].
0.43 times the strength of T7 [1] and Ptet is approximatly 2.79. [2].
 +
<br>
</p>
</p>
 +
<b>Turnover rate Ulp</b><br>
 +
<p>
 +
The parameter kcUlp is the turnover rate. It can be calculated based on in vitro specifications [5]. It is
 +
stated that 10^(-5) mg of Ulp1 cleaves 85% of 100 μg of SUMO combined with GFP in 1 hr. Furthermore
 +
the molecular weight of Ulp1 is 28 kDa and the molecular weight of SUMO is 11 kDa and the molecular
 +
weight of GFP is 27 kDa.
 +
<br>
 +
<center>
 +
<img src="https://static.igem.org/mediawiki/2013/e/ea/Equation2.png" >
 +
</center>
 +
</p>
 +
</html>
</html>

Revision as of 14:51, 15 August 2013

Timer Plus Sumo


In this section the system of Figure 1 is modeled. The structure of the timer is very similar version of the timer compared to the construct of iGEM TU Delft team 2009. Here the input is changed to a T7 promoter and the output to Ulp-1. Furthermore, the Ulp-1 cleaves off the SUMO from the peptide combined with the SUMO.


Figure 1: Circuit of the timer including sumo cleaving

Differential Equations

The above circuit can be represented by the following differential equations. We assume a binary behavior of the T7 promoter. In the presence of IPTG, the T7 promoter will be active. So, we make the assumption that the T7 is binary variable with two possible states: either active 1 or inactive 0, this is the variable s.


Parameters


Transcription rates of T7

For the T7 promoter an transcription rate of 50 bp/sec [2] converted to per minute using an average base pair length of 720 bp:


Relative promoter strength

The promoter strengths of cI and Tet are taken as a factor of T7. PcI is found to be approximatly 0.43 times the strength of T7 [1] and Ptet is approximatly 2.79. [2].

Turnover rate Ulp

The parameter kcUlp is the turnover rate. It can be calculated based on in vitro specifications [5]. It is stated that 10^(-5) mg of Ulp1 cleaves 85% of 100 μg of SUMO combined with GFP in 1 hr. Furthermore the molecular weight of Ulp1 is 28 kDa and the molecular weight of SUMO is 11 kDa and the molecular weight of GFP is 27 kDa.