Chassis
In our project, we used E.coli BW25113 strain with OmpA gene knocked out for the reason that the absence of OmpA protein would lead to hyper-vesiculation, meaning increased production of outer membrane vesicles (OMVs).
Inside the periplasm there is a thin, rigid peptidoglycan(PG) layer attached to both outer membrane and cytoplasmic membrane by membrane anchored proteins.[Fig. 1](1) Deletion or truncation of OmpA, an abundant protein linking the outer membrane and peptidoglycan layer, will therefore result in increased vesiculation in E. coli, Salmonella, and Vibrio cholerae (2) as the Figure 1 lack of OmpA destabilises the periplasm’s structure.This will result in greater likelihood that our Cas9 protein will be encapsulated into OMVs.
Importing Proteins into Periplasm Through TAT Pathway
To allow proteins to be encapsulated in OMVs, they need to be imported into bacteria’s periplasm first. Compared to other common transporting pathways that transport proteins before folding (e.g. Sec and SRP-dependent pathways), twin arginine transport (TAT) pathway is an available option for transportation of fully folded proteins(3). This is crucial since some proteins, including GFP, cannot fold properly when transported into periplasm(3).
Thus, they have to complete their folding in cytoplasm before they can be transported to periplasm. Consequently, TAT pathway is the only plausible option[Fig. 2]. Regarding the Cas9 proteins, since there has been no literature discussing the possibility of their possible
Figure 2 of folding in periplasm, we chose TAT pathway for Cas9 proteins as well out of prudence.
Testing TorA Signal Peptide Efficiency
TorA is one of the signal peptides that trigger TAT pathway. The addition of TorA to the recombinant proteins can enable the transportation of protein to periplasm.
In order to test TorA’s working efficiency, we first fused it with GFPmut3 for more convenient reading. Then we transformed plasmids with TorA-GFP into E.coli. After cultivating the transformed E.coli overnight, osmotic shock assay would be carried out to separate cytoplasm and periplasm, thereby enabling a direct reading of the latter as high degree of fluorescent light in the periplasm indicates the robustness and efficiency of TorA.
Four sets of samples are needed:
- WT with GFP
- ΔOmpA with GFP
- WT with TorA-GFP
- ΔOmpA with TorA-GFP
We used plate reader to measure the fluorescence value of both periplasmic and cytoplasmic fractions and calculate their fluorescent ratio (periplasm : cytoplasm) in order to take background noises into account. We expect the ratio to be approximately sample 3＞sample 4＞sample 2≈sample1, for the bacteria with TorA-GFP should have a larger amount of GFP in periplasm. Lower fluorescence reading in sample 4 than sample 3 indicates higher yield of OMVs in ΔOmpA strain as more GFP are encapsulated by OMVs and leave periplasm.
CjCas9
Since OMVs generally have a limited capacity as they only have a size ranging from 50nm to 200nm, proteins should be as small as possible for them to be encapsulated into OMVs. Recently characterized cjCas9(derived from Campylobacter.jejuni), with a sequence length of 2.95Kbp making it one of the smallest Cas9 orthologues, became our first choice. Moreover, cjCas9 has a high specificity, cleaving only a limited and particular number of sites in human and mouse genome (4), thereby making it a safer candidate for its application in mammals..
sgRNA
PAM
Due to conflicting reports on the PAM sequence of cjCas9, we adopted the most up-to-date results: 5‘-NNNVRYM-3’ PAM with the preference for T and C at positions 6 and 7 (5). There are many ‘PAM’ sites in FadA. Among them, we chose the one closest to 5’ as the cleaving site, in hope that the introduction of indels caused by cjCas9’s cleavage should disrupt most of FadA’s reading frame, rendering it non-functional.
crRNA
The CRISPR guide RNA (crRNA) is a type of RNA that enables CRISPR proteins to locate their targets. For an enhanced efficacy and on-target rate at knocking out fadA by our cjCas9, the design of crRNA is very important. Unlike most of Cas9 orthologues, cjCas9 recognizes the PAM nucleotides on both the target and non-target DNA strands. Our crRNA is designed to recognized the PAM strand.
We copy the rest of the sgRNA[Fig.3] sequence according to Crystal Structure of the Minimal Cas9 from Campylobacter jejuni Reveals the Molecular Diversity in the CRISPR-Cas9 Systems.
Testing cjCas9’s cleavage efficiency
After cjCas9 recognizing the cleavage site on FadA gene, a double-stranded break shall be introduced to the fadA gene, thus triggering DNA repair through nonhomologous end joining(NHEJ)[Fig.4]. NHEJ causes nearly random insertion and deletion mutations (i.e. indels) at the double-stranded break site, and thus leading to gene knockout (e.g., by causing a shift in the target gene’s reading frame or mutating a critical region of the encoded protein) (6).
To detect FadA’s frameshift, we fused a part of FadA with a mRFP protein using a GILQSTVPRARNP linker (7), creating a FadA-linker-mRFP segment. If cjCas9 successfully cleaved mRFP and resulted in a frameshift, mRFP would cease to functioning, thereby weakening the fluorescence. Subsequently, sequencing was carried out to test if cjCas9 did cause a mutation that does not affect the reading frame.
Biobrick
CjCas9[Fig. 5] is under the control of ptet-tetR promoter. The backbone consists of a pSC101 origin (yellow) and a Chloramphenicol resistant gene (light green).
sgRNA[Fig. 6] is under the control of J23100 promoter. It is inserted in pSB1A3 vector.
