IGEM:Imperial/2010/Output module: Difference between revisions

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(Moving effectors from fast response page to output page)
m (removing outdated task assignments)
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* ensure - colourless -> colour
* ensure - colourless -> colour
|-
|-
   | [[IGEM:Imperial/2010/Fast_Response_module/Target_Proteases | Target proteases ]] to use: Piotr, Nick, Kyasha
   | [[IGEM:Imperial/2010/Fast_Response_module/Target_Proteases | Target proteases ]] to use
* not many AA
* not many AA
* non-toxic
* non-toxic
* can work in E.Coli
* can work in E.Coli
* quantize speed, efficiency
* quantize speed, efficiency
   | Protein scaffold: Maddie
   | Protein scaffold
   |Fret pairs as back up for effectors
   |Fret pairs as back up for effectors
|-
|-

Revision as of 01:57, 20 July 2010

Effector 1 (Protease) Effector 2 (Dye,Enz) Pigment biosynthetic pathways
transcr sigma 54 2 colourless Billins
Activation (phosphorylation) Enz-in-pathway
  • short pathways
  • ensure - colourless -> colour
Anthocyanins
  • short pathways
  • ensure - colourless -> colour
Target proteases to use
  • not many AA
  • non-toxic
  • can work in E.Coli
  • quantize speed, efficiency
Protein scaffold Fret pairs as back up for effectors
2C DNA binding prot release

This review article has some useful information on FRET.


James- some suggested papers:

  1. Kerppola TK. Complementary methods for studies of protein interactions in living cells. Nat Methods. 2006 Dec;3(12):969-71. DOI:10.1038/nmeth1206-969 | PubMed ID:17117150 | HubMed [1]
  2. Wehr MC, Laage R, Bolz U, Fischer TM, Grünewald S, Scheek S, Bach A, Nave KA, and Rossner MJ. Monitoring regulated protein-protein interactions using split TEV. Nat Methods. 2006 Dec;3(12):985-93. DOI:10.1038/nmeth967 | PubMed ID:17072307 | HubMed [2]

All Medline abstracts: PubMed | HubMed