Team:EPF Lausanne
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- | The 2014 EPFL iGEM team has been working on showing that | + | The 2014 EPFL iGEM team has been working on showing that genetically 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 response to stimuli. 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 E. | + | 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. In E.coli, we engineered the Cpx Pathway - a two-component regulatory system responsive to envelope stress. In S.cerevisiae, we modified the HOG Pathway - a MAPKK pathway responsive to osmotic stress. 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>. If you are a judge, you might also be interested in our <a target="_blank" href="https://2014.igem.org/Team:EPF_Lausanne/Results">result page</a>, our <a target="_blank" href="https://2014.igem.org/Team:EPF_Lausanne/Judging">judging form</a> and our <a target="_blank" href="https://2014.igem.org/Team:EPF_Lausanne/Data">data page</a>.</p> |
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Revision as of 19:58, 14 October 2014
Our project in a nutshell
The 2014 EPFL iGEM team has been working on showing that genetically 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 response to stimuli. 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.
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. In E.coli, we engineered the Cpx Pathway - a two-component regulatory system responsive to envelope stress. In S.cerevisiae, we modified the HOG Pathway - a MAPKK pathway responsive to osmotic stress. To learn more about the various components of our project, check out our overview section. If you are a judge, you might also be interested in our result page, our judging form and our data page.
Envelope stress responsive bacteria
Can't touch this
Yeast
Discover how we took advantage of 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 S.Cerevisiae leading to light emission when pressure is applied.
I.T
I like turtles.
Human practice
Are we human, or are we dancers ?
Safety
work in progress
MEET OUR TEAM
We are a group of 14 students from the faculties of Life, Biomechanical, and Computer Sciences, and are supervised by 2 EPFL professors, 1 Lecturer and 5 PhD students.