Coding

Part:BBa_K4035001:Design

Designed by: Anissa Hammi   Group: iGEM21_EPFL   (2021-08-30)
Revision as of 18:11, 21 October 2021 by Hammi (Talk | contribs) (→‎Design Notes)


CUP1 fused to Aga2 and tagged with a V5 epitope


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal PstI site found at 319
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 376
    Illegal PstI site found at 319
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 562
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal PstI site found at 319
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal PstI site found at 319
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

The start and stop codon of the CUP1 genomic sequence were removed before inserted in the plasmid in order to fuse the protein to Aga2 and V5.

Source

The CUP1 (BBa_M45090) sequence is the genomic sequence of the copper metallotionein 1 protein and was inserted in the pCTcon2_V5 plasmid that was already containing Aga2, V5 tag and the Gal1 promoter.

References

(1) Chao, G.; Lau, W. L.; Hackel, B. J.; Sazinsky, S. L.; Lippow, S. M.; Wittrup, K. D. Isolating and Engineering Human Antibodies Using Yeast Surface Display. Nat Protoc 2006, 1 (2), 755–768. https://doi.org/10.1038/nprot.2006.94.