Coding

Part:BBa_K1486055:Design

Designed by: EPFL iGem team 2014   Group: iGEM14_EPF_Lausanne   (2014-10-07)


CheY/CheZ + split fLuc


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal PstI site found at 1497
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 1205
    Illegal PstI site found at 1497
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 2101
    Illegal BamHI site found at 1144
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal PstI site found at 1497
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal PstI site found at 1497
    Illegal AgeI site found at 979
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI site found at 961
    Illegal SapI.rc site found at 1805


Design Notes

When designing the part, we took care of adding a start codon at the beginning of the C terminus part of the split luciferase and deleting the stop codon at the end of the same sequence.

The two fusion proteins for the experiment mentionned in the main page are on the same plasmid. They are separated by a short random sequence followed by a second RBS.

Source

Both parts of the split were obtained from part BBa_K325108 [[1]] from Cambridge 2010 team.

CheY sequence was obtained from part BBa_K569017 [[2]] from UT Dallas 2011 team.

CheZ sequence was obtained from part BBa_K629003 [[3]] from SYSU China 2011 team.

References

Luker KE, Smith MC, Luker GD, Gammon ST, Piwnica-Worms H, Piwnica-Worms D., (August 17, 2004), Kinetics of regulated protein-protein interactions revealed with firefly luciferase complementation imaging in cells and living animals