Difference between revisions of "Team:Waterloo"

Line 11: Line 11:
 
         </div>
 
         </div>
 
         <div class="col-sm-6">
 
         <div class="col-sm-6">
             <img src="/wiki/images/1/1c/Waterloo_crispier_logo.png" alt="Waterloo iGEM CRISPieR Logo" class="img-responsive"/>
+
             <img src="/wiki/images/1/1c/Waterloo_crispier_logo.png" alt="Waterloo iGEM CRISPieR Logo" align="center" class="img-responsive">
 
         </div>
 
         </div>
 
     </div>
 
     </div>

Revision as of 01:45, 15 September 2015

Swappable sgRNA Targets | Engineered PAM Flexibility | Antiviral Protection for Plants

Waterloo iGEM CRISPieR Logo

Re-engineering CRISPR-Cas9 with functional applications in eukaryotic systems

CRISPR-Cas9 is an exciting tool for synthetic biologists because it can target and edit genomes with unprecedented specificity. Our team is attempting to re-engineer CRISPR to make it more flexible and easier to use.

We’re making it easy to test different sgRNA designs: restriction sites added to the sgRNA backbone allow 20 nucleotide target sequences to be swapped without excessive cloning.

Additionally, we’re applying recent research on viable mutations within Cas9’s PAM-interacting domain to design (d)Cas9 variants that bind to novel PAM sites, moving towards the goal of a suite of variants that can bind any desired sequence. We believe our re-engineered CRISPR-Cas9 will give biologists increased ability to optimize targeting in many applications.

The application we chose to explore is a proof-of-concept antiviral system defending the model plant Arabidopsis thaliana against Cauliflower Mosaic Virus, which would benefit from testing a large number of possible sgRNAs in the viral genome.

Top