Team:EPF Lausanne/Data

From 2014.igem.org

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To validate this hypothesis we set ourselves three intermediate objectives:
To validate this hypothesis we set ourselves three intermediate objectives:
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<u>First intermediate objective:</u> explore if and how CpxR dimerizes in live E.Coli by analyzing the various orientations of CpxR - IFP1.4 fusions.
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<u>First intermediate objective:</u> Explore if and how CpxR dimerizes in live E.Coli by analyzing the various orientations of CpxR - IFP1.4 fusions.
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<u>Third intermediate objective:</u> Analyse the spatial dynamics of the functional CpxR - IFP1.4 fusion protein by microscopy.
<u>Third intermediate objective:</u> Analyse the spatial dynamics of the functional CpxR - IFP1.4 fusion protein by microscopy.
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To validate these three objectives, we designed three experiments:
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<u>First Experiment:</u> Build constructs with all the possible orientations between CpxR and IFP1.4 and monitor activation upon 50mM KCl stress activation
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<u>Second Experiment:</u> Induce signal activation by stressing C-termina CpxR - split IFP1.4 constructs with 50 mM KCl, and subsequently replacing the media with a 0 mM KCl solution
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<u>Third Experiment:</u> Analyse the spatial dynamics of the functional CpxR - IFP1.4 fusion protein by microscopy.

Revision as of 23:28, 11 October 2014

DATA



Bacterial Biosensors


General Objective: Develop a fast and specific biosensor allowing spatiotemporal analysis of stimuli


To achieve the objective mentioned above, we put forward the following hypothesis:

Hypothesis: Combining protein complementation techniques (split IFP1.4) to proteins going through dimerization (CpxR) upon activation due to a given stimuli (enveloppe stress) allows fast and specific spatiotemporal analysis of a stimuli.


To validate this hypothesis we set ourselves three intermediate objectives:

First intermediate objective: Explore if and how CpxR dimerizes in live E.Coli by analyzing the various orientations of CpxR - IFP1.4 fusions.

Second intermediate objective: Analyse the temporal dynamics of the functional CpxR - IFP1.4 fusion protein by change of media.

Third intermediate objective: Analyse the spatial dynamics of the functional CpxR - IFP1.4 fusion protein by microscopy.

To validate these three objectives, we designed three experiments:

First Experiment: Build constructs with all the possible orientations between CpxR and IFP1.4 and monitor activation upon 50mM KCl stress activation

Second Experiment: Induce signal activation by stressing C-termina CpxR - split IFP1.4 constructs with 50 mM KCl, and subsequently replacing the media with a 0 mM KCl solution

Third Experiment: Analyse the spatial dynamics of the functional CpxR - IFP1.4 fusion protein by microscopy.

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