IGEM:MIT/2005/Receiver 1: ToxR: Difference between revisions
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#how will we design a system to find more bigger antigen sets? | #how will we design a system to find more bigger antigen sets? | ||
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# Can we solve the cell wall permeability problem? | |||
==Need Help With== | ==Need Help With== |
Revision as of 13:26, 13 July 2005
Receiver Device #1 -- ToxR
POC
wiki-Will
Function
To dimerize in the presence of the input signal and cause gene expression to turn on.
Device Depiction
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ToxR Pathway
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Edit ToxR.ppt
Information path ...
- Fluoroscein introduced to system (as Fluoroscein+DNAspacer+Fluoroscein), travels into periplasm.
- Fluoroscein binds to adjacent ToxR'-scFv fusions.
- Causes ToxR' dimerization
- GFP expressed @ CTX_promoter
- As a function of ToxR dimerization
People path ...
- Maxine gives us Fluoroscein, or identifies something else
- Maxine's antigen binds to Jenny's scFv
- Then, Jenny's scFv induces Will's ToxR' to dimerize
- The dimerization leads to the expression of Jessica's output @ CTXpromoter [cI, maybe]
- Ray makes the whole system look like "we meant to do that."
- Jen makes sure it all works.
Device Parts
Current Status
- About to order all necassary proteins and primers for first synthesis.
- Begin design and outline necassary experiments for system.
- Develop brief yet throrough system explanation.
- Need to verify that we can get our signal into the periplasm
- Recieve olgo's 07/13. LEts throw them in our cells
- and if it doesn't "just work," develop and specify how we have to manipulate / weaken our cells to make it work.
- lets make it WORK
- Continue'd research on putting our scFv onto the outermembrane of a cell.
Open Issues/Questions
- !
- How will we get our initial test antigens into our cell?
- how will we design a system to find more bigger antigen sets?
- Can we solve the cell wall permeability problem?