Difference between revisions of "Team:Waterloo"

m
m
Line 19: Line 19:
 
{{Waterloo}}
 
{{Waterloo}}
 
<html>
 
<html>
     <h2>CRISPieR: re-engineering CRISPR-Cas9 with functional applications in eukaryotic systems</h2>
+
     <h2>Re-engineering CRISPR-Cas9 with functional applications in eukaryotic systems</h2>
 
     <p>
 
     <p>
 
         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.
 
         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.
Line 34: Line 34:
  
  
     <p class="desc-links" style="text-align:center;">
+
     <p class="desc-links" style="text-align:center;margin-bottom:85px;">
 
         <a href="/Team:Waterloo/Sitemap">Sitemap</a>
 
         <a href="/Team:Waterloo/Sitemap">Sitemap</a>
 
     </p>
 
     </p>

Revision as of 22:13, 14 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