Team:EPF Lausanne

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<h1 class="cntr"> Our project in a nutshell</h1>
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The 2014 EPFL iGEM team has been working on showing that biologically engineered organisms can detect and process signals quickly and efficiently. With this in mind, our team brought forward a novel idea: combining protein complementation techniques with biosensors to achieve fast spatiotemporal analysis of cell responses to stimuli. In other words, we fused complementary reporter protein fragments to interacting proteins. The presence of a given stimulus leads to the interaction of the proteins of interest thus allowing the fused split complements to re-acquire their functional conformation and emit signal. We thereby are able to detect signal dynamics by relying on much faster post-transcriptional modifications rather than slow traditional reporter transcription.
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we are able to detect signal dynamics thanks to the association of the reporter fragments. We thereby rely on much faster post-transcriptional modifications to generate signals rather than traditional reporter transcription.
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The principle is the following: two complementary fragments of a reporter protein are fused to interacting proteins. When the interaction is stimulated, the two fragments associate, thereby reconstituting the reporter signal in a much faster way than traditional post-transcriptional reporters.
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As a proof-of-concept, we aimed to develop the first BioPad: a biological trackpad made of a microfluidic chip, touch-responsive organisms and a signal detector. To make our organisms touch-sensitive, we engineering two stress-related pathways in <i>E. coli</i> and <i>S. cerevisiae</i>.<!--In <i>E. coli</i>, we engineered the Cpx Pathway - a two-component regulatory system responsive to envelope stress. In <i>S. cerevisiae</i>, we modified the HOG Pathway - a MAPKK pathway responsive to osmotic stress.--> As for the reporter proteins, we worked mainly with fluorescent proteins but also implemented a split luciferase complementation assay. To learn more about the various components of our project, check out our <a target="_blank" href="https://2014.igem.org/Team:EPF_Lausanne/Overview">overview section</a>, as well as the different <a target="_blank" href="https://2014.igem.org/Team:EPF_Lausanne/Parts">parts</a> submitted by our team. If you are a judge, you might also be interested in our <a target="_blank" href="https://2014.igem.org/Team:EPF_Lausanne/Results">results page</a>, our <a target="_blank" href="https://2014.igem.org/Team:EPF_Lausanne/Data">data page</a> and our <a target="_blank" href="https://2014.igem.org/Team:EPF_Lausanne/Judging">judging form</a>. </p>
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<h2>Why a BioPad?</h2>
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<p class="lead">The biological concepts behind the BioPad project have applications in basic and applied sciences. From a scientific perspective, the ideas introduced and implemented by our project are novel and promising for future applications. The BioPad is also an interesting concept that will encourage public awareness of synthetic biology. The tangibility of the project will allow the general public to look at synthetic biology in a better way, as people will understand how great genetically modified organisms are! To get down the basics, the combination of novel biological concepts, a cool idea, and the community awareness that our project provides, makes the BioPad project perfect an ideal project for iGEM!
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<h2>The BioPad's Applications</h2>
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<p class="lead">With respect to basic sciences, the BioPad demonstrates that protein complementation techniques are suitable for biosensors – especially for two-component regulatory systems. The introduction of the split IFP1.4 (infrared fluorescent protein) into the registry will allow future iGEM and research teams to take advantage of the reversibility and precision of this protein. Moreover, our work on the Cpx pathway will allow future iGEM teams to make novel uses of other members of this subfamily, as well as other two-component regulatory systems.
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As for applied sciences, the BioPad could be used to deliver a cheap, fast, efficient, and accurate antibiotic screening system allowing researchers to easily quantify the effects of antibiotics on gram-negative bacteria. The BioPad project could also be the source of an "antibiotic complement" drug increasing the efficiency of pre-existing antibiotics. Moreover, the Biopad could provide a new approach to studying genes by allowing researchers to examine the relationship between genes and their corresponding activating signals. To learn more about the applications of our project click <a target="_blank" href="https://2014.igem.org/Team:EPF_Lausanne/Applications">here</a>.</p>
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<!-- Most sciences are able to detect and process signals in a fast and efficient way. Biology lacks this ability as signal detection and processing requires large amounts of time leading to potential inaccuracies and interferences from external sources. We aim to improve this and make signal induction faster and more accurate in biological contexts. In this sense, the 2014 EPFL iGEM team worked on developing a -->
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<!--As a proof of concept we aim to design touch responsive bacteria designing an innovating new biological machine using protein complementation techniques.</p> -->
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<!-- <p class="lead">As a proof of concept of this new way of viewing biology, this year’s EPFL iGEM team aims to build the first biological touchpad, hereafter referred as the BioPad, allowing users to control electronics in real time through living organisms.</p>  -->
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  <p class="lead">Find out how we took advantage of the Cpx pathway and split IFP1.4 to give birth to bacteria emitting fast signals in response to chemical and mechanical stresses!</p>
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        <img src="https://static.igem.org/mediawiki/2014/b/b3/Beer.png" alt="Yeast" />
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        <h1>Osmo responsive yeast</h1>
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  <p class="lead">Discover how we engineered the HOG osmotic response pathway to create touch sensitive yeast strains! Learn more on how we implemented a split GFP and a split Luciferase in <i>S. cerevisiae</i> leading to light emission when pressure is applied.</p>
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  <p class="lead">Our Biopad is implemented in a microfluidic chip. This tool allows all kinds of analytical experiments
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  this awesome device here!</p>
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  <p class="lead">In order to process our data quickly and automatically, we built an interface with a Raspberry Pi and a camera. Discover how <br />it works by clicking here!</p>
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  <p class="lead">Our project is well suited to show the general public the power of synthetic biology. Find out how we introduced this domain to the younger generation, and how they developed their own mini iGEM projects to tackle everyday problems with enthusiasm and creativity.</p>
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<p class="lead">The first microfluidic design that provides<br /> total on-chip waste decontamination: discover<br /> how we tackled biosafety issues by<br /> engineering an awesome device!</p>
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<div class="span6"><h1 class="cntr">MEET OUR TEAM</h1>
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<p>We are a group of 13 students from the faculties of Life Sciences & Technologies and Computer Sciences, </br>and are supervised by 2 EPFL professors, 1 Lecturer and 5 PhD students.</p></div>
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Latest revision as of 03:50, 18 October 2014

Our project in a nutshell




EPFL_interaction_IFP_cartoon
Association of split IFP 1.4 fragments

The 2014 EPFL iGEM team has been working on showing that biologically engineered organisms can detect and process signals quickly and efficiently. With this in mind, our team brought forward a novel idea: combining protein complementation techniques with biosensors to achieve fast spatiotemporal analysis of cell responses to stimuli. In other words, we fused complementary reporter protein fragments to interacting proteins. The presence of a given stimulus leads to the interaction of the proteins of interest thus allowing the fused split complements to re-acquire their functional conformation and emit signal. We thereby are able to detect signal dynamics by relying on much faster post-transcriptional modifications rather than slow traditional reporter transcription.

As a proof-of-concept, we aimed to develop the first BioPad: a biological trackpad made of a microfluidic chip, touch-responsive organisms and a signal detector. To make our organisms touch-sensitive, we engineering two stress-related pathways in E. coli and S. cerevisiae. As for the reporter proteins, we worked mainly with fluorescent proteins but also implemented a split luciferase complementation assay. To learn more about the various components of our project, check out our overview section, as well as the different parts submitted by our team. If you are a judge, you might also be interested in our results page, our data page and our judging form.

MEET OUR TEAM

We are a group of 13 students from the faculties of Life Sciences & Technologies and Computer Sciences,
and are supervised by 2 EPFL professors, 1 Lecturer and 5 PhD students.

the team's students

Sponsors