Team:EPF-Lausanne/Team
From 2009.igem.org
(→Who we are) |
(→What we want to do) |
||
Line 49: | Line 49: | ||
Light-sensitive proteins can easily be found in nature. | Light-sensitive proteins can easily be found in nature. | ||
- | + | In this project, our aim is to design a fusion/hybrid protein that would allow genetic regulation through light control. | |
Therefore we are working on cloning strategies that would allow us to fuse natural "wild" light-sensitive domains with regulatory proteins. The idea is to allow transmission of the conformational change induced by light (on the light-sensitive domain) to the DNA-binding domain. This transmitted conformational change would then result in an increase or decrease of the regulatory domain's affinity for the DNA promoter site. | Therefore we are working on cloning strategies that would allow us to fuse natural "wild" light-sensitive domains with regulatory proteins. The idea is to allow transmission of the conformational change induced by light (on the light-sensitive domain) to the DNA-binding domain. This transmitted conformational change would then result in an increase or decrease of the regulatory domain's affinity for the DNA promoter site. | ||
- | The | + | The overal effect would thus be a genetic expression controlled by light! |
Revision as of 11:57, 14 July 2009
Who we are
Advisors:
|
Where we are from
We are all studying at EPFL aka the Swiss Institute of Technology of Lausanne. The campus is located near the shore of lake Geneva in the surroundings of the city of Lausanne, 50 km away from Geneva.
What we want to do
Light-sensitive proteins can easily be found in nature.
In this project, our aim is to design a fusion/hybrid protein that would allow genetic regulation through light control.
Therefore we are working on cloning strategies that would allow us to fuse natural "wild" light-sensitive domains with regulatory proteins. The idea is to allow transmission of the conformational change induced by light (on the light-sensitive domain) to the DNA-binding domain. This transmitted conformational change would then result in an increase or decrease of the regulatory domain's affinity for the DNA promoter site.
The overal effect would thus be a genetic expression controlled by light!