Difference between revisions of "Part:BBa K1997024"
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| − | Figure | + | Figure 2. Prokaryotic expression and protein purification of split-HRP-dCas9 fusion proteins. |
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| + | (A) Expression and purification of sHRP-C-dCas9 protein. (B) Expression and purification of sHRP-N-dCas9 protein. Western blots were probed with an anti-His-tag antibody. “-” represents the un-induced control group, “+” represents the induced group. | ||
===References=== | ===References=== | ||
Latest revision as of 01:12, 21 October 2016
P+R->sHRP-N->dCas9->Ter
This part codes a fusion protein of sHRP-N and dCas9
Usage and Biology
A catalytically dead Cas9 (dCas9) formed a DNA recognition complex which can bind any sequence when co-expressed with a guide RNA. 1
HRP was used as a reporter,the enzymatic activity of split fragments would be reconstituted when they were reassembled. 2
In our project, we used engineered E.coli to produce the fusion protein of dCas9 and split-HRP fragments.
Sequence and Features
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 415
Illegal NheI site found at 2038 - 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 657
Illegal BamHI site found at 4317 - 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Experimental Validation
This part is validated through two ways: PCR and functional testing
PCR
Methods
The PCR is performed with Premix EX Taq by Takara.
F-Prime: 5’- GAATTCGCGGCCGCTTCTAGAATGC-3’
R-Prime: 5’- GGACTAGTATTATTGTTTGTCTGCC-3’
The PCR protocol is selected based on the Users Manuel. The Electrophoresis was performed on a 1％ Agarose glu. The result of the agarose electrophoresis was shown on the picture below.
Functional Test
The plasmid was transformed into the E.coli BL21 (DE3) competent cells. After a overnight culture with (or without, as control group) 0.5mM IPTG induction, cells were collected and lysed by high pressure homogenizer. Subsequent purification was performed by nickel-nitrilotriacetic acid agarose affinity chromatography according to the standard protocol. As examined by SDS-PAGE and Western blots (probed with an anti-His-tag antibody), both of these proteins were successfully expressed and purified as a high degree of purity up to 90%.
Figure 2. Prokaryotic expression and protein purification of split-HRP-dCas9 fusion proteins.
(A) Expression and purification of sHRP-C-dCas9 protein. (B) Expression and purification of sHRP-N-dCas9 protein. Western blots were probed with an anti-His-tag antibody. “-” represents the un-induced control group, “+” represents the induced group.
References
1. Lei S. Qi, Matthew H. Larson, Luke A. Gilbert et al. Repurposing CRISPR as an RNA-guided platform for sequence-specific control of gene expression. Cell, 2013, 152: 1173-1183. 2. Kathryn E. Luker, Matthew C. P. Smith, et al. Kinetics of regulated protein–protein interactions revealed with firefly luciferase complementation imaging in cells and living animals. PNAS, 2004, 101: 12288-12293.