Difference between revisions of "Part:BBa K3017011"

Revision as of 15:16, 17 October 2019

dCas9-6XHis

The CRISPR associated protein, in our case, dCas9, is a non-specific deactivated endonuclease. dCas9 is catalytically dead with mutations D10A and H840A. It binds to the target protein, when coupled with single-guide RNA, but does not induce any DNA breakage as in Cas9 enzyme.

In our project, Combined CRISPRi and antisense RNA Toggle Switch, dCas9 plays a central role in CRISPR interference. dCas9 acts as an agent of steric hindrance to block mRNA polymerization to repress expression levels of target genes.

Cloning

As one of the most important components of our circuit, dCas9 needed to be cloned and expressed in the cells. The dCas9 sequence used was kindly given by Dr. Hi Yi Mak, an associate professor of life science in HKUST who also have worked with dCas9. However, the sequence of that dCas9 was noticed to have 5 PstI cut sites within the coding sequence meaning that the standard assembly method using EcoRI, XbaI, SpeI and PstI would not be compatible. We thus have added a SalI cut site after PstI to replace PstI by PCR. The other basic parts (BBa_K608006 and BBa_B0015) that is used in subcloning were also added with the SalI cut site. The three parts were then constructed in a BBa_PSB1C3 vector to form a dCas9 expressing vector.

Figure1. PCR verification of dCas9 transformed cells

Two chloramphenicol selected colonies were picked and inoculated in 5ml of LB and incubated in 37℃ for overnight. The cultures were then extracted with plasmid and checked by PCR with VRII and VR primers. A band appeared in between 4 to 5 Kb showed success in transformation. The expected DNA size was 4.6 Kb

Transformation and expression of dCas9 in DH5-α E.coli

The resulting plasmid was then transformed into DH5α E. coli using heat shock, and cells were selected by chloramphenicol followed by Miniprep plasmid extraction and PCR verification (Figure. 1).

Following transformation, we further went on checking the expression of dCas9. Cell lysis was prepared by sonication in NP-40 lysis buffer. The protein concentration of the lysis was checked by Bradford Assay against the BSA standard curve (Figure. 2). 10ul of cell lysis was used to run through the SDS-PAGE (5% stacking, 6% resolving). After the electrophoresis, the gel was stained with Coomassie Blue to visualize the protein (Figure. 3). As shown in the gel, there is an extra band much larger than 82kDa exist only in the dCas9 transformed cells but not appear in the cells transformed with an empty vector.

Figure. 2 BSA Standard Curve and Calculated protein concentration of lysis

Figure 3. dCas9 expression check with SDS-PAGE and Coomassie Blue staining

Cell lysis were prepared by overnight growing in 5ml LB under 37&#8451 followed sonication in NP-40 lysis buffer. 10ul of cell lysis was mixed with 10ul of loading buffer and run through an SDS-PAGE(5% stacking and 6% resolving). Coomassie blue was then used to visualize the bands. An extra band larger than 82kDa can be seen only in the dCas9 transformed cells.

To further verify if that extra band is really the dCas9, we repeated the experiment again with all the condition remain the same except that instead of visualizing by Coomassie Blue, we changed to use western blot targeting the 6XHis tag at the C-terminal of dCas9. The western blotting was done using a His-probe Antibody (1:2000, Rabbit) and a secondary HRP-goat anti-rabbit antibody (1:2000). 500ul of ECL detection reagents (Amersham) was then added and the band can subsequently be visualized using light-sensitive X-ray films. As shown in the figure, a clear band only appeared in the dCas9 transformed cells verifying the extra band shown in figure 2 is indeed the dCas9.

Sequence and Features