Team:Grenoble/Modeling/Conclusion
From 2012.igem.org
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- | In the amplification module, we saw that we could get a signal if there was more than 10<SUP>-6</SUP> mol | + | In the amplification module, we saw that we could get a signal if there was more than 10<SUP>-6</SUP> mol.L<span class="exposant">-1</span> of initial cAMP. In the signaling part, we saw that when the dipeptide is detected, it will lead to the production of adenylate cyclase. Then, when the adenylate cyclase is produced, it leads to the production of cAMP, and this will launch the amplification module. Thus, we will have: |
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- | We notice that for an initial concentration of dipeptide around 10<SUP>-8,5</SUP> mol | + | We notice that for an initial concentration of dipeptide around 10<SUP>-8,5</SUP> mol.L<span class="exposant">-1</span> of dipeptide we can get a signal. If we make the conversion in number of molecule (we multiply by the Avogadro number (=6,02*10<SUP>23</SUP> mol.L<span class="exposant">-1</span>) and by the volume of the cell (given in the quorum sensing part = 10<SUP>-15</SUP> L), we obtain that our detection threshold is around 20 molecules. |
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Revision as of 21:05, 25 September 2012
How does the entire system work?
Now, we need to answer two questions:- Is the sensitivity of the amplification module satisfying regarding to the quantity of adenylate cyclase that the signaling module can create?
- What is the time of answer of our system?