Team:EPF Lausanne/Next steps

From 2013.igem.org

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• Engineer a fusion protein between ice nucleation protein and <br>
• Engineer a fusion protein between ice nucleation protein and <br>
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But we didn't have enough time to characterize and assemble the parts completely.
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But we didn't have enough time to characterize completely and assemble the parts to form the Taxi.Coli.
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Revision as of 08:47, 4 October 2013

Taxi.Coli: Smart Drug Delivery iGEM EPFL

Header

Up until now we succeded
• Producing Nanoparticles and loading them
• Clone a pH sensitive promoter
• Engineer a fusion protein between ice nucleation protein and

But we didn't have enough time to characterize completely and assemble the parts to form the Taxi.Coli.

Contents

What we would have done with more time:

Nanoparticles




Cell surface display of Streptavidin

• Cloned a plasmid that encodes a fusion protein INP-Streptavidin-YFP and one INP-YFP-Streptavidin. Then we would have been able to use the exact same protocol we used to characterize the Biobrick BBa_K523013, to proof surface localization.


Sensing/Effector




Taxi.Coli

• Cloned one of our Biobricks in a backbone that contains another resistance than chloramphenicol to cotransfect bacteria with the Plasmids responsible for Sensing/Effector and the Plasmid used to connect the Nanoparticles.