LOVTAP

From 2009.igem.org

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<span style="color:grey">letter :[[Media:letter_T.R.Sosnick.pdf]]
<span style="color:grey">letter :[[Media:letter_T.R.Sosnick.pdf]]
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<i><font size=3> in vitro </font size></i>
 
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<i><font size=3> in vitro </font size></i>
<i><font size=3> in vivo </font size></i>
<i><font size=3> in vivo </font size></i>

Revision as of 20:19, 3 June 2009

To get

URGENT: get starting material


in vitro

- Sequence of the 12 mutant fusion proteins or LOV domain AND TrpR (separately) => Pubmed
- Purification kit
- Digestion assay protocol
- LED/light sources or photometer
- Calmodulin kit or stuffs for protection assay


in vivo
- Inducible promoter (IPTG or Lac repressor)
- Reporter cassette mCherry or RFP

To do: theory

- Write an e-mail to Strickland et al to ask Basile first shot; I think we could then look at it all together

letter :Media:letter_T.R.Sosnick.pdf


in vitro

in vivo

- Find the exact genetic circuit for Trp repressor Nath

An interesting course on TrpR and Trp operon: TrpR

- 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.

To do: wet lab


in vitro

- Redo the experiment they did in the LOVTAP article

!!! Major problem, the conformational change of LOVTAP is weak and the protection assay results show a small difference of LOVTAP binding on DNA between drak state and light state !!! ----> try to improve this

Express and purify mutants
is flavin indispensable??
Trp has to be added
- Do a mutational assay to change or enhance specificity of LOVTAP
</b>
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


in vivo

Express LOVTAP under control of an inducible promoter
Link a reporter cassette with TrpR binding domain



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