Difference between revisions of "Team:Northwestern"
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<h2>Our Project</h2> | <h2>Our Project</h2> | ||
| − | <p>Our team is investigating the utility of outer membrane vesicles (OMVs) in the delivery of Cas9 in vivo. All Gram-negative bacteria produce OMVs and use them to deliver toxins, communicate with other bacteria, mediate membrane composition, and extract materials such as metal ions from their environment. OMVs have been successfully engineered to carry heterologous proteins,<a href="#_msocom_1" name="_msoanchor_1" id="_msoanchor_1"><sup> | + | <p>Our team is investigating the utility of outer membrane vesicles (OMVs) in the delivery of Cas9 in vivo. All Gram-negative bacteria produce OMVs and use them to deliver toxins, communicate with other bacteria, mediate membrane composition, and extract materials such as metal ions from their environment. OMVs have been successfully engineered to carry heterologous proteins,<a href="#_msocom_1" name="_msoanchor_1" id="_msoanchor_1"><sup>1</sup></a> which makes them an attractive candidate for systems that require the delivery of a functional protein or complex to recipient cells. One such system is the application of CRISPR-Cas9 to treating antibiotic-resistant bacterial infections. At the moment no mechanism exists to deliver functional Cas9 to target cells, with the nearest alternative being bacteriophage delivery. This system requires recipient cells to synthesize Cas9 themselves and is limited to species that are susceptible to bacteriophage infection. We hope to use signal peptides and protein fusions to direct Cas9 into OMVs so that the functional complex can be delivered to and act on the resistance genes in antibiotic-resistant bacteria.</p> |
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<h3>References</h3> | <h3>References</h3> | ||
<div class="references"> | <div class="references"> | ||
| − | <p><a name="_msocom_1" id="_msocom_1"></a><a href="#_msoanchor_1">[1]</a> Kuehn, Meta J, and Nicole C Kesty. “Bacterial Outer Membrane Vesicles and the Host-Pathogen Interaction.” | + | <p><a name="_msocom_1" id="_msocom_1"></a><a href="#_msoanchor_1">[1]</a> Kuehn, Meta J, and Nicole C Kesty. “Bacterial Outer Membrane Vesicles and the Host-Pathogen Interaction.” Genes & Development 19.22 (2005): 2645–55. <a href="http://www.ncbi.nlm.nih.gov/pubmed/14578354" target="_blank">Web</a>.</p> |
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Revision as of 19:39, 22 June 2016
Our Project
Our team is investigating the utility of outer membrane vesicles (OMVs) in the delivery of Cas9 in vivo. All Gram-negative bacteria produce OMVs and use them to deliver toxins, communicate with other bacteria, mediate membrane composition, and extract materials such as metal ions from their environment. OMVs have been successfully engineered to carry heterologous proteins,1 which makes them an attractive candidate for systems that require the delivery of a functional protein or complex to recipient cells. One such system is the application of CRISPR-Cas9 to treating antibiotic-resistant bacterial infections. At the moment no mechanism exists to deliver functional Cas9 to target cells, with the nearest alternative being bacteriophage delivery. This system requires recipient cells to synthesize Cas9 themselves and is limited to species that are susceptible to bacteriophage infection. We hope to use signal peptides and protein fusions to direct Cas9 into OMVs so that the functional complex can be delivered to and act on the resistance genes in antibiotic-resistant bacteria.
References
