Coding

Part:BBa_K2065007

Designed by: Tom van Sonsbeek   Group: iGEM16_TU-Eindhoven   (2016-10-10)
Revision as of 09:21, 18 October 2016 by Tjvsonsbeek (Talk | contribs) (LargeBiT-GGS10-CT52 Statistics)

CT52-LargeBiT

The CT52-LargeBiT BioBrick is part of a split luciferase system. This luciferase system consists of two parts, namely SmallBiT and LargeBiT. It is a ATP-independent luciferase, that produces high intensity luminescence. The total weight is 19.1 kDa. The NanoLuc system consists of 171 amino acids. When they dimerize, this means when they come into close proximity of each other, one can see luminescence. The emission peak of this NanoBiT system is around 460 nanometers. This is blue light.

Usage and Biology

LargeBiT is linked to CT52 with a GGS10-linker, so it actually consists of 3 subparts. LargeBiT is 477 basepairs long and thus consists of 159 amino acids. The GGS10-linker that is used, consists of 30 amino acids, it is a ten-times repeated sequence of Glycine-Glycine-Serine amino acids. This complex is linked to CT52. This protein consist of the last 52 amino acids of the C-terminal region of the H+-ATPase. The N-terminus of CT52 is a free end, which can be used to link proteins to. The binding between CT52 and T14-3-3 is stabilized by the small molecule Fusicoccin. When Fusicoccin is present, the affinity of CT52 for T14-3-3 is increased in 30 fold with respect to the situation when Fusicoccin is not present [3]. The binding interaction with Fusicoccin is reversibel, this means CT52 will dissociate from the scaffold.

This means that the CT52-GGS10-LargeBiT construct will move towards the scaffold protein, after a small molecule, Fusicoccin, is added. Three different variants of the CT52-protein were created with the help of the Rosetta software package. Each mutation in the CT52 protein has its complementary mutation in the T14-3-3 protein. Because these mutations were found with the help of the Rosetta software package, the quality of these mutations have to be verified. One variant of the C52 protein was already known and tested. This mutation functioned as a positive control in the verification process of the other mutations.


Sequence

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 730
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]

Bioluminescence confirmation

To determine whether the split luciferase system is working, one should see a luminescence signal when the two components come into close proximity of each other. A luminescence peak around 460nm must be visible when SmallBiT and LargeBiT dimerize.

When the two NanoBiTs are into close proximity of each other, they dimerize. When Furimazine is added to the dimerized Nanoluc luciferase, the Furimazine is converted into Furimamide. When this reaction occurs, light with a wavelength of 460 nm will be emitted.

CT52-LargeBiT statistics

Protein Specifications
General Information Number of amino acids 241
Molecular weight 25770.01
Theoretical pi 5.14
Extinction coefficient 21430
Formula C1140H1807N313O359S4
Total numbers of atons 3623
Amino Acid Composition Amino Acid Frequency Percentage(%)
Ala(A) 11 4.6
Arg(R 9 3.7
Asn(N) 11 4.6
Asp(D) 12 5.0
Cys(C) 0 0
Gln(Q) 11 4.6
Glu(E) 16 6.6
Gly(G) 35 14.5
His(H) 5 2.1
Ile(I) 19 7.9
Leu(L) 20 8.3
Lys(K) 11 4.6
Met(M) 4 1.7
Phe(F) 8 3.3
Pro(P) 7 2.9
Ser(S) 19 7.9
Thr(T) 13 5.4
Trp(W) 2 0.8
Tyr(T) 7 2.9
Val(V) 21 8.7
Pyl(O) 0 0.0
Sec(U) 0 0.0



[edit]
Categories
//awards/basic_part/nominee
Parameters
None