Difference between revisions of "Part:BBa K5382150:Design"
 
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===Detail considerations in the design process===
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__NOTOC__
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In the initial design, we successfully achieved the co-expression of Cas9 enzyme and its associated guide RNA in E. coli, but later we found that this method still has some limitations, mainly in the low yield and long purification time.
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<partinfo>BBa_K5382150 short</partinfo>
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In order to improve the yield of Cas9 RNPs, we introduced the CL7 label on the n-terminal of the original Cas9. The CL7 tag can be easily recognized by human rhinovirus (HRV) 3C protease cutting at 16°C for 3 hours. In addition, to prevent contamination of the 3C protease in the final sample, we used an engineered CL7-labeled HRV 3C protease. In the expression of sgRNA, we use T7 promoter to obtain higher expression efficiency
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The pCold-CL7-Cas9 expression plasmid scheme is shown in the figure.
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https://static.igem.wiki/teams/5382/part-pictures/little-sp.png<br>'''Figure 1.'''    The pCold-CL7-Cas9 co-expression plasmid.<br>
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According to the experimental design, when IPTG was added, sgRNA molecules were transcribed in large quantities in Escherichia coli, while CL7-Cas9 fusion protein was also expressed simultaneously in Escherichia coli.
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The final results showed that the Cas9 RNPs yield was increased to ~40 mg/L using LB medium, which was 4 times higher than the existing method.
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In terms of purification methods, we introduced an ultra-high affinity CL7/ Im7 system, which helped us achieve one-step purification of Cas RNPs in half a day (supplementary Table 1, see supplementary information). Compared with Cas9 RNPs purified by Ni-NTA affinity column, the purity of Cas9 RNPs purified by Im7 column was improved from ~58% to ~89% based on gray scale scan analysis (Figure 2).
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https://static.igem.wiki/teams/5382/part-pictures/middle-sp-plus.png<br>'''Fig, 2 a.''' A total of 12% SDS-PAGE of Cas9 RNP (10 μg, red square) and Cas12a RNP (5ug. blue square) purified by Ni-NTA affinity column or by Im7 column. The original uncropped gels were shown in Supplementary Fig, 7. '''b''' The target Cas RNPs' purity was validated from three individual batches of
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purification by gray scanning analysis (ImageJ) of the SDS-PAGE. Data are shown as the mean ± SD<br>
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The various bands visible on the gel of Ni-NTA purified Cas RNPs are proteins from E. coli itself. The purity of target Cas RNPs can be improved by gradient elution of imidazole with different concentration and purification by gel filtration. Importantly, reproducible results were observed when Cas9 RNPs were prepared with different Sgrnas (supplementary Figure 7). In addition, there is no difference between batches in the production of the same Cas9 RNPs. Notably, by coupling the recombinant Im7 enzyme to agarose beads, we simply prepared Im7 affinity columns that can be repeatedly regenerated without losing the binding affinity to CL7 affinity tag16.
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With our method, no RNase inhibitors are required during the entire purification and storage process. The resulting Cas9RNP is very stable and can be stored at -20 °C for 9 months without activity changes. From this, we propose that sgRNAs transcribed in E. coli can somehow bind tightly to newborn Cas9, helping Cas9 fold into a stable conformation and protecting sgRNAs from nuclease-mediated degradation.
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===Supplementary experimental results===
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<partinfo>BBa_K5382150 SequenceAndFeatures</partinfo>
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1. Purification and in vitro activity verification of Cas9 RNP in EcN
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https://static.igem.wiki/teams/5382/part-pictures/crsipr1.png<br>'''Figure 3.'''   The mutant structure compared to the Wild type Ceres.<br>
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===Relevant factors to consider in the design process===
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'''a.''' Lane M: three-color prestain protein Marker
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In this study, we introduced a creative method for the efficient biosynthesis of Cas9 ribonucleoproteins (RNPs) using a refined <i>E. coli</i> expression system, specifically with the wild-type <i>Escherichia coli</i> Nissle 1917 (EcN) strain. Based on our previous work <sup>[1]</sup>, we have engineered an in vivo self-assembling plasmid designed for Cas9 RNP expression, where in the synthesis of both the Cas9 protein and guide RNA (gRNA) is governed by the Tac promoter, which is recognized by <i>E. coli</i> RNA polymerase. Following transformation into the wild-type EcN, the plasmid facilitated the expression of Cas9 RNP. The purified Cas9 RNP was then analyzed through in vitro enzyme activity assay (Figure 1) to assess its capacity to cleave target DNA sequences.<br>
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Lane 1: break bacteria precipitate Lane 2: Bacteria-breaking supernatant Lane 3: Flow eluent after binding with nickel beads
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<center>https://static.igem.wiki/teams/5382/part-pictures/crsipr1.png</center><br><center>'''Figure 1.'''     Purification efficiency and in vitro activity verification experiments of Cas9 RNP.</center> <br>
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Lane 4-7: different concentrations of imidazole gradient eluents '''b.''' Lane M:DNA Marker Lane 1: Target plasmid pCDNA3.1-Flag-PRDX4 Lane 2: pCold-Cl7-Cas9-P4 experimental group Lane 3:spel single enzyme digestion
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'''a.''' Lane M: Pre-stained protein marker; Lane 1: Target plasmid PCDNA3.1-Flag-PRDX4; Lane2: pCold-Cas9-P4 experimental group; Lane3: SpeI single enzyme digestion; Lanes 4-7: Gradient elution with different concentrations of imidazole: 20 mM, 50 mM, 300 mM, 300 mM.<br>
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'''b.''' Lane M: DNA Marker; Lane 1: The target plasmid; Lane 2: cleaved plasmid by Cas9 RNP; Lane 3: Cleaved plasmid by Spe I.<br>
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Our experimental findings reveal that the purity of Cas9 ribonucleoproteins (RNPs), as determined by nickel column chromatography, was approximately 80% and displayed adequate cleavage activity on target plasmids. However, the yield was suboptimal. Specifically, the use of the Tac promoter for Cas9 RNP synthesis yielded approximately 1 mg per liter of culture medium, which was markedly lower than anticipated. Our analysis indicates that the low yield may be due to the relatively weak activity of the Tac promoter, which likely resulted in reduced transcription of gRNA and, consequently, diminished assembly and enzymatic activity of the Cas9 RNP complexes. The WT EcN strain does not possess T7 RNA polymerase, which is necessary for recognizing the stronger T7 promoter. Consequently, to enhacne the gRNA expression and the assembly efficiency of Cas9 RNP complexes, we then designed an experiment to incorporate the T7 RNA polymerase gene into the EcN genome (Figure 2).<br>
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<center>https://static.igem.wiki/teams/5382/part-pictures/45.png</center><br><center>'''Figure 2.''' The schematics of the expression plasmid for Cas9 RNP with a T7 promoter</center>
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We purified the engineered EcN strain and successfully isolated Cas9 RNPs utilizing the T7 promoter. Subsequently, the enzymatic cleavage activity of the isolated Cas9 RNPs was confirmed via in vitro nuclease assay (Figure 3), indicating an extraordinary nuclease activity. A comparative analysis of the yield of Cas9 RNPs produced using the T7 promoter versus the Tac promoter was performed and is illustrated in Figure 4. The results demonstrated that the expression level of Cas9 RNPs reached 8 mg per liter of culture medium, representing an approximately 8-fold increase compared to that achieved using the Tac promoter.
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<center>https://static.igem.wiki/teams/5382/part-pictures/23.png</center> <br><center>'''Figure 3.''' In vitro cleavage of the target plasmid.</center><br>
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Lane M DNA Marker ; Lane 1 Target plasmid; Lane 2 Cleaved plasmid by XbaI; Lane 3 Cleaved plasmid by Cas9 RNP.
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<center>https://static.igem.wiki/teams/5382/part-pictures/22.png</center><br><center>'''Figure 4.'''  Comparative analysis of Cas9 RNP production using T7 and Tac promoters after purification.</center><br>
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Next, we utilized a well-established engineering technique to generate outer membrane vesicles (OMVs) from genetically modified EcN, employing the lipid extruder method. The OMVs were subsequently purified and their size was characterized using transmission electron microscopy (TEM) and dynamic light scattering (DLS). Our findings confirm the successful assembly of Cas9 RNP-loaded OMVs by the engineered EcN, with an average particle diameter of approximately 100 nm (Figure 5).<br>
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<center>https://static.igem.wiki/teams/5382/part-pictures/15.png<br></center><center>'''Figure 5.''' TEM image analysis and DLS analysis results of OMVs.</center><br>
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After confirming the expression levels and enzymatic activity of Cas9 RNPs, as well as evaluating the efficiency of their delivery system (OMS), we proceeded to explore their potential applications in cellular genome editing, which are elaborated in the Experimental section.<br>
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===Source===
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We have achieved the co-expression of Cas9 enzyme and its related guide RNA(gRNA) in <i>Escherichia coli</i> Nissle 1917. The Cas9 protein is derived from <i>Streptococcus pyogenes</i> (<i>S. pyogenes</i> Cas9, SpCas9). The gRNA and Cas9 protein expression sequences in the system are constructed on the same plasmid, and the plasmid backbone is the pCold vector. The gRNA is artificially designed according to the sequence of the targeted gene PRDX4 and can specifically bind to its sequence.<br>
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===References===
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[1] Qiao J, Li W, Lin S, Sun W, Ma L, Liu Y. Co-expression of Cas9 and single-guided RNAs in Escherichia coli streamlines production of Cas9 ribonucleoproteins. Commun Biol. 2019; 2:161.Published 2019 May 3. doi:10.1038/s42003-019-0402-x

Latest revision as of 13:38, 2 October 2024

Cas9 ribonucleoproteins(gRNA PRDX4)-Co-expression and self-assembly of RNPs


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 4514
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]

Relevant factors to consider in the design process

In this study, we introduced a creative method for the efficient biosynthesis of Cas9 ribonucleoproteins (RNPs) using a refined E. coli expression system, specifically with the wild-type Escherichia coli Nissle 1917 (EcN) strain. Based on our previous work [1], we have engineered an in vivo self-assembling plasmid designed for Cas9 RNP expression, where in the synthesis of both the Cas9 protein and guide RNA (gRNA) is governed by the Tac promoter, which is recognized by E. coli RNA polymerase. Following transformation into the wild-type EcN, the plasmid facilitated the expression of Cas9 RNP. The purified Cas9 RNP was then analyzed through in vitro enzyme activity assay (Figure 1) to assess its capacity to cleave target DNA sequences.

crsipr1.png

Figure 1. Purification efficiency and in vitro activity verification experiments of Cas9 RNP.

a. Lane M: Pre-stained protein marker; Lane 1: Target plasmid PCDNA3.1-Flag-PRDX4; Lane2: pCold-Cas9-P4 experimental group; Lane3: SpeI single enzyme digestion; Lanes 4-7: Gradient elution with different concentrations of imidazole: 20 mM, 50 mM, 300 mM, 300 mM.
b. Lane M: DNA Marker; Lane 1: The target plasmid; Lane 2: cleaved plasmid by Cas9 RNP; Lane 3: Cleaved plasmid by Spe I.

Our experimental findings reveal that the purity of Cas9 ribonucleoproteins (RNPs), as determined by nickel column chromatography, was approximately 80% and displayed adequate cleavage activity on target plasmids. However, the yield was suboptimal. Specifically, the use of the Tac promoter for Cas9 RNP synthesis yielded approximately 1 mg per liter of culture medium, which was markedly lower than anticipated. Our analysis indicates that the low yield may be due to the relatively weak activity of the Tac promoter, which likely resulted in reduced transcription of gRNA and, consequently, diminished assembly and enzymatic activity of the Cas9 RNP complexes. The WT EcN strain does not possess T7 RNA polymerase, which is necessary for recognizing the stronger T7 promoter. Consequently, to enhacne the gRNA expression and the assembly efficiency of Cas9 RNP complexes, we then designed an experiment to incorporate the T7 RNA polymerase gene into the EcN genome (Figure 2).


45.png

Figure 2. The schematics of the expression plasmid for Cas9 RNP with a T7 promoter

We purified the engineered EcN strain and successfully isolated Cas9 RNPs utilizing the T7 promoter. Subsequently, the enzymatic cleavage activity of the isolated Cas9 RNPs was confirmed via in vitro nuclease assay (Figure 3), indicating an extraordinary nuclease activity. A comparative analysis of the yield of Cas9 RNPs produced using the T7 promoter versus the Tac promoter was performed and is illustrated in Figure 4. The results demonstrated that the expression level of Cas9 RNPs reached 8 mg per liter of culture medium, representing an approximately 8-fold increase compared to that achieved using the Tac promoter.




23.png

Figure 3. In vitro cleavage of the target plasmid.

Lane M DNA Marker ; Lane 1 Target plasmid; Lane 2 Cleaved plasmid by XbaI; Lane 3 Cleaved plasmid by Cas9 RNP.





22.png

Figure 4. Comparative analysis of Cas9 RNP production using T7 and Tac promoters after purification.

Next, we utilized a well-established engineering technique to generate outer membrane vesicles (OMVs) from genetically modified EcN, employing the lipid extruder method. The OMVs were subsequently purified and their size was characterized using transmission electron microscopy (TEM) and dynamic light scattering (DLS). Our findings confirm the successful assembly of Cas9 RNP-loaded OMVs by the engineered EcN, with an average particle diameter of approximately 100 nm (Figure 5).


15.png
Figure 5. TEM image analysis and DLS analysis results of OMVs.

After confirming the expression levels and enzymatic activity of Cas9 RNPs, as well as evaluating the efficiency of their delivery system (OMS), we proceeded to explore their potential applications in cellular genome editing, which are elaborated in the Experimental section.

Source

We have achieved the co-expression of Cas9 enzyme and its related guide RNA(gRNA) in Escherichia coli Nissle 1917. The Cas9 protein is derived from Streptococcus pyogenes (S. pyogenes Cas9, SpCas9). The gRNA and Cas9 protein expression sequences in the system are constructed on the same plasmid, and the plasmid backbone is the pCold vector. The gRNA is artificially designed according to the sequence of the targeted gene PRDX4 and can specifically bind to its sequence.

References

[1] Qiao J, Li W, Lin S, Sun W, Ma L, Liu Y. Co-expression of Cas9 and single-guided RNAs in Escherichia coli streamlines production of Cas9 ribonucleoproteins. Commun Biol. 2019; 2:161.Published 2019 May 3. doi:10.1038/s42003-019-0402-x