Part:BBa_K2450201
TetR with TEV cleavage site and CFP tag
This part is a modified TetR repressor protein containing a cleavage site for TEV protease. It offers a new way of relieving repression of a DNA system. The cleavage site is located in the linker between the DNA binding domain and dimerisation domain of TetR. It also has a His-tag for easy purification in a nickel column. It is an improvement of a previous iGEM part.
The TetR repressor is only functional as a dimer. Each monomer has a DNA-binding domain and a dimerisation domain.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Usage and Biology
TetR functions as a homodimer to bind tet operator sequences and prevent the association of RNA polymerase with its promoter. Each TetR monomer has a DNA binding domain and a dimerisation domain. The DNA binding domain is a helix-turn-helix motif that associates with a tet operator sequence (TCCCTATCAGTGATAGAGA). Our complementary part, BBa_K2450301, contains 2 repeats of this sequence - one for each monomer.
TEV protease has a specific cleavage site of Glu-Asn-Leu-Tyr-Phe-Gln-(CUT)-Gly, which was inserted into our protein in a linker region between the DNA binding domain and the dimerisation domain.
On PyMOL, we identified the different domains of the TetR monomer, and identified a suitable linker for cleavage. On the image to the left, the DNA binding domain is coloured in blue, the dimerisation domain is pink, and the linker which has been modified is in grey.
References
Orth, P et al. Structural basis of gene regulation by the tetracycline inducible Tet repressor−operator system Nature Structural Biology 7, 215 - 219 (2000) doi:10.1038/73324
Ramos JL, Martínez-Bueno M, Molina-Henares AJ, et al. The TetR Family of Transcriptional Repressors. Microbiology and Molecular Biology Reviews. 2005;69(2):326-356. doi:10.1128/MMBR.69.2.326-356.2005.
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