Team:Leeds

From 2013.igem.org

(Difference between revisions)
Line 18: Line 18:
<br>
<br>
-
 
In order to achieve this we will have designed our biosensor to physically bind to the antigen of interest. This will induce membrane stress which activates the Cpx pathway. By putting the GFP gene downstream of the Cpx promoter, GFP protein will be made when membrane stress occurs and consequently the cells will fluoresce when the pathogen is present in the solution.  
In order to achieve this we will have designed our biosensor to physically bind to the antigen of interest. This will induce membrane stress which activates the Cpx pathway. By putting the GFP gene downstream of the Cpx promoter, GFP protein will be made when membrane stress occurs and consequently the cells will fluoresce when the pathogen is present in the solution.  
<br>
<br>
-
 
As a proof of concept, first we will be using silica beads as a pathogen analogue. In order to bind to the beads will be express a silica binding peptide on the surface of the cells using ice nucleation protein. INP, a BioBrick we decided to use from the registry, expresses any gene sequence placed at its C terminus on the cell surface. The theory is that the silica binding peptide sequence can be easily swapped for a sequence of any antigen binding moiety and therefore enable us to detect any pathogen, simply, quickly and cheaply.  
As a proof of concept, first we will be using silica beads as a pathogen analogue. In order to bind to the beads will be express a silica binding peptide on the surface of the cells using ice nucleation protein. INP, a BioBrick we decided to use from the registry, expresses any gene sequence placed at its C terminus on the cell surface. The theory is that the silica binding peptide sequence can be easily swapped for a sequence of any antigen binding moiety and therefore enable us to detect any pathogen, simply, quickly and cheaply.  
<br>
<br>
}}
}}

Revision as of 10:35, 9 August 2013

Parky roof.png
Parky top.png
Back to iGEM Main Page
Welcome to the Leeds Wiki!
Parky main.png
iGEM Leeds Facebook
iGEM Leeds Twitter
iGEM Leeds Youtube
Leeds socialbanneredge.png
Parky tower.png
awesome looking header



Who the heck are Leeds?

Leeds is a city in West Yorkshire, in the North of England. It has strong historical ties to the wool industry, and is famous for the Tetley brand of bitter ale
We are the Leeds 2013 iGEM team, We are a group of undergrads from various courses all with a passion for synthetic biology!


So what's the Big Idea?

Like the hunting dog, the Beagle, our Micro-beagle is a biosensor designed to hunt down pathogens. Micro-beagle utilises the Cpx pathway and GFP, which, when it fluoresces can be seen with the naked eye.


In order to achieve this we will have designed our biosensor to physically bind to the antigen of interest. This will induce membrane stress which activates the Cpx pathway. By putting the GFP gene downstream of the Cpx promoter, GFP protein will be made when membrane stress occurs and consequently the cells will fluoresce when the pathogen is present in the solution.


As a proof of concept, first we will be using silica beads as a pathogen analogue. In order to bind to the beads will be express a silica binding peptide on the surface of the cells using ice nucleation protein. INP, a BioBrick we decided to use from the registry, expresses any gene sequence placed at its C terminus on the cell surface. The theory is that the silica binding peptide sequence can be easily swapped for a sequence of any antigen binding moiety and therefore enable us to detect any pathogen, simply, quickly and cheaply.

Parky base.png
Geneious, our fine sponsors and suppliers of software Bioline, our fine sponsors and suppliers of equipment Qiagen, our fine sponsors and suppliers of PCR kits
Bangs Laboratories, our fine sponsors and suppliers of silica beads
Leeds Homepage