Team:EPF-Lausanne/Human Practices

From 2011.igem.org

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Instead of reaching to the whole population, we decided to use the Human Practices for introducing the iGEM community to microfluidics. Being from a technology institute, we took advantage of our university's expertise to use microfluidics chips in our project.
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Instead of reaching out to the general population, we decided to use the Human Practices for introducing the iGEM community to microfluidics. Being from a technology institute, we took advantage of our university's expertise to use microfluidics chips in our project.
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Microfluidics technology is a powerful tool for biological research, having a wide range of applications. Here is a non-exhaustive list:
Microfluidics technology is a powerful tool for biological research, having a wide range of applications. Here is a non-exhaustive list:
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* DNA-protein interactions: to determine the binding affinity of a transcription factor or to discover new regulatory proteins
* DNA-protein interactions: to determine the binding affinity of a transcription factor or to discover new regulatory proteins
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All these applications share the same advantages: reduced volumes allowing reagents cost reduction, parallelization of the experiments and high-throughput screening. In vitro gene synthesis is very expensive normally, but working on a small scale for microfluidics makes it more affordable. The MITOMI chip we used contains 768 wells, all visible at once, allowing to test hundreds of protein-protein combinations at once. You can flow DNA, proteins, molecule libraries and other chemical reagents on microfluidics devices - allowing big creativity.
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These experiments share the same advantages when ported on-chip: reagent volumes are reduced, therefore minimising cost, and the tiny size of each reaction chamber allows massive parallelisation of the experiment, leading to high-throughput screening. More specifically, ''in vitro'' gene synthesis becomes affordable at this scale, and the MITOMI chip we used contains 768 wells, all visible in one frame, which allowed us to quantify affinity of hundreds of protein-DNA combinations in a single picture. The small channels also allow fine control over reaction conditions. Most soluble reagents can be used, including DNA, proteins, molecule libraries, and so on - allowing much creativity in experimental design.
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Only a few iGEM teams used or are using this technology for this project. We believe that promoting microfluidics would help the teams, allowing them to save time and have better tools for characterization. To this end, we wrote detailed explanations on how to set up your own chip in the [https://2011.igem.org/Team:EPF-Lausanne/Tools/Microfluidics/HowTo1 Tools section]. We also created a [https://2011.igem.org/Team:EPF-Lausanne/Tools/Microfluidics/Tamagotchip microfluidics game], consisting of a chip located in our lab that iGEMers can control via their computers.
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Few iGEM teams used this technology for their projects. We believe that promoting the use microfluidics can help iGEM and improve the Parts Registry, specifically by providing more thorough part characterisation. To this end, we wrote a guide to get started with microfluidics, focusing on how to build a setup [[Team:EPF-Lausanne/Tools/Microfluidics/HowTo2|build a setup]] and outlining [[Team:EPF-Lausanne/Tools/Microfluidics/HowTo1|chip fabrication]]. To tickle the community's interest, we also created a [[Team:EPF-Lausanne/Tools/Microfluidics/Tamagotchip|live online microfluidics game]], where iGEMers can control a chip located in our lab from their web browser.
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Revision as of 18:11, 21 September 2011