Difference between revisions of "Part:BBa K2226005"
 
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c-Myc promoter, FK-506-binding protein 12 fused to c-terminal of split luciferase (Cluc394), acts as one half of a promoter-reporter system, forms FRB-rapamycin-FKBP complex in presence of rapamycin.
 
c-Myc promoter, FK-506-binding protein 12 fused to c-terminal of split luciferase (Cluc394), acts as one half of a promoter-reporter system, forms FRB-rapamycin-FKBP complex in presence of rapamycin.
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The FKBP-Cluc part was taken from the 2015 Peking iGEM team, and we further characterized it by attaching a gene-specific promoter for c-Myc gene, altering the shape.
  
 
In order to test the construct, we combined the COX-2 promoter-reporter construct with the c-Myc promoter-reporter construct in a solution with COX-2 and c-Myc gene constructs to model the conditions in the bodies of patients with CRC, where an excess of COX-2 and c-Myc protein is shed. As shown in the figures below, the combination of the COX-2 promoter-FRB-nLuc construct, c-Myc promoter-FKBP-cLuc construct in the presence of rapamycin and free-floating COX-2 and c-Myc protein successfully induced glowing.  
 
In order to test the construct, we combined the COX-2 promoter-reporter construct with the c-Myc promoter-reporter construct in a solution with COX-2 and c-Myc gene constructs to model the conditions in the bodies of patients with CRC, where an excess of COX-2 and c-Myc protein is shed. As shown in the figures below, the combination of the COX-2 promoter-FRB-nLuc construct, c-Myc promoter-FKBP-cLuc construct in the presence of rapamycin and free-floating COX-2 and c-Myc protein successfully induced glowing.  
  
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In addition, to make sure the construct worked only with all components present (protein and
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In addition, to make sure the construct worked only when all were components present (gene constructs, promoter-reporter system, rapamycin) we tested out multiple combinations where certain components to show proof of concept. The figures show that glowing was induced only with all the components present, proving that our construct can detect COX-2 and c-Myc proteins.
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rapamycin) we tested out multiple combinations with and without rapamycin, as well as each individual construct with rapamycin and without rapamycin on their own. The figures show that glowing was induced only with all the components present, proving that our construct can detect COX-2 and c-Myc proteins.
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https://static.igem.org/mediawiki/parts/e/e9/Results_plates.png
 
https://static.igem.org/mediawiki/parts/e/e9/Results_plates.png

Latest revision as of 11:21, 31 October 2017


c-Myc promoter - FKBP - Cluc394

c-Myc promoter, FK-506-binding protein 12 fused to c-terminal of split luciferase (Cluc394), acts as one half of a promoter-reporter system, forms FRB-rapamycin-FKBP complex in presence of rapamycin.

The FKBP-Cluc part was taken from the 2015 Peking iGEM team, and we further characterized it by attaching a gene-specific promoter for c-Myc gene, altering the shape.

In order to test the construct, we combined the COX-2 promoter-reporter construct with the c-Myc promoter-reporter construct in a solution with COX-2 and c-Myc gene constructs to model the conditions in the bodies of patients with CRC, where an excess of COX-2 and c-Myc protein is shed. As shown in the figures below, the combination of the COX-2 promoter-FRB-nLuc construct, c-Myc promoter-FKBP-cLuc construct in the presence of rapamycin and free-floating COX-2 and c-Myc protein successfully induced glowing.

In addition, to make sure the construct worked only when all were components present (gene constructs, promoter-reporter system, rapamycin) we tested out multiple combinations where certain components to show proof of concept. The figures show that glowing was induced only with all the components present, proving that our construct can detect COX-2 and c-Myc proteins.

Results_plates.png Results_solution.png

Above image showqualitative results demonstrate the constructs combining successfully in the presence of rapamycin when transformed in E. coli on plates and expanded in solution.


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 45
    Illegal NheI site found at 68
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 688
    Illegal AgeI site found at 827
  • 1000
    COMPATIBLE WITH RFC[1000]