Difference between revisions of "Part:BBa K3187008"
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Revision as of 08:49, 16 October 2019
GGGG-Tag for Sortase-mediated Ligation x mCherry Fluorescence Protein
Profile
Name | mCherry-LPETGG |
Base pairs | 1028 |
Molecular weight | 28.5 kDa |
Origin | synthetic, derived from Discosomasp. |
Parts | mCherry, T7-promoter, GGGG-sequence, lac-operator, GASPAG, Strep-Tag II, T7-terminator |
Properties | Red fluorescent, Ex λ: 587nm, Em λ: 610 nm |
Usage and Biology
mCherry (BBa_K3187026)is a red
fluorescent
protein.
Which is a synthetic protein derived from Discosoma sp. by
directed evolution. The N-terminal GGGG-sequence (BBa_K3187018)
can be fused to a protein with a C-terminal LPETGG-Sortase A link target="_blank">(BBa_K3187019)
by Sortase A. We use mCherry as an easily imaged reporter for checking if the coupling worked.
The coding sequence was cloned in pDest vector, containing the sequence of mCherry, a GASPAG-Linker
(BBa_K3187038), a
Strep-Tag II (BBa_K3187025)
for
Purification, a T7 promoter with lac-operator and an RBS (BBa_K3187029), a T7TE terminator (BBa_K3187032), a
GGGG-sequence, a Start-Codon (BBa_J70593)
and a Stop-Codon (BBa_K2868029)(). The
coding sequence consists of 851 bp which are translated to 260 amino acids.[1]
Methods
Purification
The GGGG-mCherry was heterologously expressed in E. coli BL21 and purified with GE Healthcare ÄKTA Pure machine which is a machine for FPLC. The used affinity tag was Strep-tagII.
SDS-Page and Western blot
To verify that the CP-LPETGG was produced, a SDS-Page SDS-Page followed by a Western blot was performed.
Results
Cloning and Expression
The successful cloning was proven with sanger sequencing and production with a Western blot.
Fig. 1 shows that the band of the GGGG-mCherry is approximatley found by the 28.5 kDa band. Consequently, the successful protein production was proven.CP-LPETGG is detected with Strep-Tactin-HRP.
References
- 10INCOMPATIBLE WITH RFC[10]Illegal PstI site found at 854
- 12INCOMPATIBLE WITH RFC[12]Illegal PstI site found at 854
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 915
- 23INCOMPATIBLE WITH RFC[23]Illegal PstI site found at 854
- 25INCOMPATIBLE WITH RFC[25]Illegal PstI site found at 854
- 1000COMPATIBLE WITH RFC[1000]