Team:Grenoble/Project/Abstract
From 2012.igem.org
(Difference between revisions)
m |
|||
(3 intermediate revisions not shown) | |||
Line 6: | Line 6: | ||
<div id="cadre"> | <div id="cadre"> | ||
<section> | <section> | ||
- | <h1> | + | <h1>sEnsiColi: A tunable and reliable ultra-sensitive detector</h1> |
- | + | ||
- | + | Multi-resistant bacteria are a worldwide issue which in a very near future will have | |
+ | huge impacts on our societies and ways diagnosis and prevention will be performed. | ||
+ | In this optic, the Grenoble iGEM team has built an ultra-sensitive pathogen detector. | ||
+ | <br/><br/>It consists of three interconnected modules: | ||
<ol> | <ol> | ||
- | + | <li>Detection</li> | |
- | + | <li>Amplification/Communication</li> | |
- | + | <li>Output</li> | |
</ol> | </ol> | ||
<br/> | <br/> | ||
- | The detection module | + | The detection module consists of a recombinant membrane receptor that, once activated, actuates an amplification loop. The amplification system contains a genetic feed forward loop, which filters out false |
- | The amplification system contains a genetic feed forward loop | + | positive outputs. Once amplified and filtered, the signal is transmitted to neighboring |
- | <br/> | + | bacteria via a diffusible molecule. In turn, the amplification loop is triggered which |
- | <center> <h4>Scheme of the concept</h4> </center> | + | leads to the production of a measurable fluorescence output. <br/> |
+ | <br/>The design of our | ||
+ | network is easily adaptable to different input signals by using other receptor domains. | ||
+ | <!-- <center> <h4>Scheme of the concept</h4> </center> | ||
<center><img src="https://static.igem.org/mediawiki/2012/9/9d/Schema1.png" alt="Scheme of the concept" style="horizontal-align: center;"/></center> | <center><img src="https://static.igem.org/mediawiki/2012/9/9d/Schema1.png" alt="Scheme of the concept" style="horizontal-align: center;"/></center> | ||
<center> <h4>Theoretical response of the device depending on the input signal</h4> <br/> | <center> <h4>Theoretical response of the device depending on the input signal</h4> <br/> | ||
- | <img src="https://static.igem.org/mediawiki/2012/c/cf/Schema2.png" alt="Theoretical response of the device depending on the input signal" style="horizontal-align: center;"/></center> | + | <img src="https://static.igem.org/mediawiki/2012/c/cf/Schema2.png" alt="Theoretical response of the device depending on the input signal" style="horizontal-align: center;"/></center> --> |
</section> | </section> | ||
</div> | </div> |
Latest revision as of 00:59, 25 September 2012
sEnsiColi: A tunable and reliable ultra-sensitive detector
Multi-resistant bacteria are a worldwide issue which in a very near future will have huge impacts on our societies and ways diagnosis and prevention will be performed. In this optic, the Grenoble iGEM team has built an ultra-sensitive pathogen detector.It consists of three interconnected modules:
- Detection
- Amplification/Communication
- Output
The detection module consists of a recombinant membrane receptor that, once activated, actuates an amplification loop. The amplification system contains a genetic feed forward loop, which filters out false positive outputs. Once amplified and filtered, the signal is transmitted to neighboring bacteria via a diffusible molecule. In turn, the amplification loop is triggered which leads to the production of a measurable fluorescence output.
The design of our network is easily adaptable to different input signals by using other receptor domains.