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LOVTAP
From 2009.igem.org
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<br> Purification protocol | <br> Purification protocol | ||
<br> Digest assay protocol | <br> Digest assay protocol | ||
| - | <br><span style="color:grey">letter :[[Media: | + | <br><span style="color:grey">letter :[[Media:letter_T.R.Sosnick.pdf]] |
;- Biobricks | ;- Biobricks | ||
Revision as of 18:22, 2 June 2009
To find
- Sequence of the 12 mutant fusion proteins or LOV domain AND TrpR (separately) => [http://www.ncbi.nlm.nih.gov/ Pubmed]
To do
- - Find the exact genetic circuit for Trp repressor Nath
An interesting course on TrpR and Trp operon: [http://www2.hawaii.edu/~scallaha/SMCsite/475%20Lectures/475Lecture34.pdf TrpR]
- - Write an e-mail to Strickland et al to ask Basile first shot; I think we could then look at it all together
Sequence (of all 12 fusion proteins)
Purification protocol
Digest assay protocol
letter :Media:letter_T.R.Sosnick.pdf
- - Biobricks
Look for a (or many) paper(s) that characterizes E.Coli Trp repressor, and find the Trp operon sequence Mél
Summary of what characterizes E.Coli Trp repressor : Media:The_tryptophan_biosynthetic_pathway.pdf
One good article : RNA-based_regulation_of_genes_of_tryptophan_synthesis_an_degradation.pdf
Sequence from NCBI : Media:Sequence_du_Trp_repressor.txt
Design a biobrick that coexpresses LOVTAP and mCherry (after Trp operon) when LOVTAP bind the Trp operon. Design a switch on/off read out.
- Do a mutational assay to change specificity of LOVTAP:
- Direct mutational assay: Insert mutation in specific sites thanks to the known structure of LOVTAP (already modeled on computer)
- Indirect mutational assay: Random mutations, then selection of the "right" protein according to a set of selected conditions
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