VesiCure.
What is CRISPR-CAS9 system?
Discovered in 2012 at UC Berkely, CRISPR-CAS9 is the most powerful gene editing tool to date. When bacteria are under attack by viruses, their immune system grabs viral RNA and “tucks” the sequence into CRISPR-short for “clustered regularly interspaced short palindromic repeats” located in the viruses genome. The next time the virus attacks the bacterium is prepared: using the appropriate CRISPR sequence in the genome, a guide RNA (gRNA) is synthesized that directs a protein, Cas9, to the viral DNA. Acting as molecular scissors, the Cas-gRNA complex binds to the viral DNA and dices up the genetic material.
Why does CRISPR-CAS9 matter?
An application of CRISPR-CAS9 is that of treating drug resistant infections. CRISPR-CAS9 should be able to cut out the resistant gene in an antibiotic resistant bacterium, thereby making the bacteria susceptible to antibiotics. However, for CAS9 to be effective, it has to be successfully delivered. Our team aims to use signal peptide-protein fusions to direct Cas9 and a guiding gRNA sequence into OMVs. OMVs are naturally occurring extracellular vesicles that are used for cross talk between bacteria. Hence, they make strong candidates for transportation of Cas9/gRNA to target bacteria.