Difference between revisions of "Team:BostonU/App 2/Results"

Revision as of 22:17, 18 September 2015

Results

We were so excited to have researched SaCas9 and found potentially viable split sites. We were able to create 16 different split sites within the sequence and cloned most of these constructs into the FKBP/FRB dimerizable domains. Utilizing transient transfection we tested the full SaCas9 and traffic light reporter however there was neither GFP nor mCherry expressed, so we concluded that no double strand break had been made. We hypothesize that there was likely an issue with our choice of target sequence within the traffic light reporter. Below we have results from our flow cytometry run showing arbitrary units of fluorescence.

It is clear that even the fully functional SaCas9 did not work properly, therefore none of the subsequent split SaCas9 worked either. Although we were not able to draw any conclusions from this data in the future we would like to debug our initial SaCas9 design and then continue to validate splits in the same workflow as the integrases where we will look for patterns between split site locations, different dimerization domains, and their orientations. It would be very exciting to find viable split sites and create a system for genomic editing using split SaCas9.

Towards the end of our project, the Feng Zhang group at MIT published the crystal structure of saCas9 in Cell¹. The paper demonstrated the development of a conditionally dimerizable saCas9 system using the FKBP-FRB domain pairs and PYL-ABI domain pairs, which is what we wanted to accomplish.

One facet worth noting is that the Zhang group used the 3D structure of the saCas9 protein to target flexible linker regions that would serve as potential split sites. Out of the three split sites that they chose, the one that worked best was almost identical (one amino acid away) to one of the split sites that we identified using our model. Furthermore, the other two split sites that they chose which were not as successful happened to be located in regions with secondary structural elements.

This important result gave us some experimental validation that our model could offer scientists insights into choosing promising viable split sites for proteins, without only relying on 3D structures of proteins.

Citations

Nureki, Osamu et al., “Crystal structure of staphylococcus aureus Cas9”, Cell, 2015.

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 <h3>Results</h3>
-<p>Unfortunately, the system we designed had some errors, and we were unable to gather any useful data on our split SaCas9 experiment. We created 16 split sites within SaCas9 and cloned most of these constructs into the FKBP/FRB dimerizable domains. We tested the full SaCas9 on the traffic light reporter, and there was no fluorescence at all, so we concluded that no double stranded break had been made. We realize that there may have been an issue with our choice of target sequence within the traffic light reporter. For future analysis, we can test the SpCas9 on the traffic light reporter to see how feasible the system is before moving on to SaCas9 and split SaCas9 halves. Below, we have the fluorescence data for SaCas9. The fluorescence shown is very low and about the same throughout for all constructs, so we were unable to draw any valid conclusions based on this data.</p>
+<p>We were so excited to have researched SaCas9 and found potentially viable split sites. We were able to create 16 different split sites within the sequence and cloned most of these constructs into the FKBP/FRB dimerizable domains. Utilizing transient transfection we tested the full SaCas9 and traffic light reporter however there was neither GFP nor mCherry expressed, so we concluded that no double strand break had been made. We hypothesize that there was likely an issue with our choice of target sequence within the traffic light reporter. Below we have results from our flow cytometry run showing arbitrary units of fluorescence.<p>
+<p>It is clear that even the fully functional SaCas9 did not work properly, therefore none of the subsequent split SaCas9 worked either. Although we were not able to draw any conclusions from this data in the future we would like to debug our initial SaCas9 design and then continue to validate splits in the same workflow as the integrases where we will look for patterns between split site locations, different dimerization domains, and their orientations. It would be very exciting to find viable split sites and create a system for genomic editing using split SaCas9.</p>
 <center><img style="height:40%; width:40%;" src="https://static.igem.org/mediawiki/2015/thumb/e/e7/Sacas9_gfp.png/800px-Sacas9_gfp.png" />