Team:SJTU-BioX-Shanghai/Project/Subproject1-1

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(Result)
(Design)
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This rare tRNA<sup>Arg</sup> can be charged with Arg by native '''Arginyl-tRNA Synthetase(ArgRS)''' in E.coli.
This rare tRNA<sup>Arg</sup> can be charged with Arg by native '''Arginyl-tRNA Synthetase(ArgRS)''' in E.coli.
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[[image:11SJTU_Rare_03.jpg|center|tRNA Modulator]]
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[[image:11SJTU_Rare_03.jpg|center|Over express tRNA<sup>Arg</sup>-AGG in order to get translation of target gene through]]
'''RFP-6AGG''': we have inserted 6 AGG codons after the start codon ATG in the RFP gene.  
'''RFP-6AGG''': we have inserted 6 AGG codons after the start codon ATG in the RFP gene.  

Revision as of 16:55, 28 October 2011



  • Rare tRNA Amount

    Design

    In this part we have overexpressed rare tRNAArg-AGG in the cell. The rare tRNA can recognize AGG codon on the mRNA.

    tRNAArg-AGG: tRNAArg-AGG is over expressed under the control of trc promoter (induced by IPTG).

    This rare tRNAArg can be charged with Arg by native Arginyl-tRNA Synthetase(ArgRS) in E.coli.

    Over express tRNAArg-AGG in order to get translation of target gene through

    RFP-6AGG: we have inserted 6 AGG codons after the start codon ATG in the RFP gene.

    11SJTU rare 00.jpg

    Action

    When rare tRNAArg-AGG is not over-expressed, RFP expression is hindered. When tRNAArg-AGG is over-expressed, this tRNA can recognize the AGG codon on the mRNA so a large amount of RFP is produced.

    11SJTU rare 01.jpg



    Result

    Fig 1. Confocal Microscope examining RFP expression. RFP has been largely produced in cells overexpressing tRNAArg-AGG.
    Fig 2 Cells over-expressing tRNAArg-AGG emit bright red fluorescence as wild type RFP (first one from the left). Control (first one from the right) exhibits no red fluorescence.

    RFP has been largely produced in cells overexpressing tRNAArg. No RFP can be observed in cells without rare tRNA overexpression.

    We have successfully controlled protein expression by controlling rare tRNA amount.


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