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Team:Paris Bettencourt/GFPLac diffusion
From 2011.igem.org
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<h1>The YFP Concentration design</h1> | <h1>The YFP Concentration design</h1> | ||
| - | <p><em>YFP:tetR</em>is a recombinant fusion protein. It is composed by | + | <p><em>YFP:tetR</em> is a recombinant fusion protein. It is composed by |
Their origin come from François-Xavier Barre, Andrew Wright and Dave Lane ( -</p> | Their origin come from François-Xavier Barre, Andrew Wright and Dave Lane ( -</p> | ||
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<p>In the Ben-Yehuda paper, GFP has been proved to pass though the nanotubes. We start to build the same experiment but improved by the tetR:YFP - tetO Array system..</p> | <p>In the Ben-Yehuda paper, GFP has been proved to pass though the nanotubes. We start to build the same experiment but improved by the tetR:YFP - tetO Array system..</p> | ||
| - | <p><em>In the emittor cell</em>, we have to over express the T7 polymerase for them to have a chance to pass through the tube. As we said in the <a href="https://2011.igem.org/Team:Paris_Bettencourt/Designs">general overview</a> the production of T7 polymsease is over the control of an IPTG inducible promoter design to have a slow response by the over-expression of LacI in the cell. The RFP, placed on the same mRNA, is behaving like a reporter of the quantity of the produced T7 polymerase.</p> | + | <p><em>In the emittor cell <i>(B.Subtilis)</i></em>, we have to over express the T7 polymerase for them to have a chance to pass through the tube. As we said in the <a href="https://2011.igem.org/Team:Paris_Bettencourt/Designs">general overview</a> the production of T7 polymsease is over the control of an IPTG inducible promoter design to have a slow response by the over-expression of LacI in the cell. The RFP, placed on the same mRNA, is behaving like a reporter of the quantity of the produced T7 polymerase.</p> |
<p><em>In the receiver cell</em>, a system, sensitive to the T7 polymerase will be activated if one T7 polymerase reach on of its promoter, present in a few plasmids of the receiver cell (low copy). The system is self amplifying and the GFP is produced as a monitor of the signal.</p> | <p><em>In the receiver cell</em>, a system, sensitive to the T7 polymerase will be activated if one T7 polymerase reach on of its promoter, present in a few plasmids of the receiver cell (low copy). The system is self amplifying and the GFP is produced as a monitor of the signal.</p> | ||
Revision as of 16:11, 11 September 2011
The YFP Concentration design
YFP:tetR is a recombinant fusion protein. It is composed by Their origin come from François-Xavier Barre, Andrew Wright and Dave Lane ( -
In our designs, we wanted a protein to pass through the tube and trigger a signal in the receiver cell. We see here that T7 RNA polymerase si a very good candidate for sugh system. That's why we used as the biggest of our proof of principle molecules.
Making the YFP:tetR diffuse through the tube
In the Ben-Yehuda paper, GFP has been proved to pass though the nanotubes. We start to build the same experiment but improved by the tetR:YFP - tetO Array system..
In the emittor cell (B.Subtilis), we have to over express the T7 polymerase for them to have a chance to pass through the tube. As we said in the general overview the production of T7 polymsease is over the control of an IPTG inducible promoter design to have a slow response by the over-expression of LacI in the cell. The RFP, placed on the same mRNA, is behaving like a reporter of the quantity of the produced T7 polymerase.
In the receiver cell, a system, sensitive to the T7 polymerase will be activated if one T7 polymerase reach on of its promoter, present in a few plasmids of the receiver cell (low copy). The system is self amplifying and the GFP is produced as a monitor of the signal.
The principle of the design is summed up in the image below
Model and experiments
To know more about what we have done on this system and in the experiments, we invite you to visit the correcponding modeling and experiment pages:
