Team:CU-Boulder

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<!-- Header -->
 
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<h1 id="logo"><a href="#">iGEM CU-Boulder</a></h1>
 
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<ul>
 
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<li><a href="https://2014.igem.org/Team:CU-Boulder#intro">Project</a>
 
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                                                            <ul><li>
 
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                                                            <a href="https://2014.igem.org/Team:CU-Boulder/Learning">Overview</a></li><li>
 
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                                                            <a href="https://2014.igem.org/Team:CU-Boulder/Results">Results</a></li><li>
 
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                                                            <a href="https://2014.igem.org/Team:CU-Boulder/Notebook">Notebook</a></li>
 
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                                                            </ul>
 
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                                                        </li><li>
 
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<a href="https://2014.igem.org/Team:CU-Boulder/Achievements">Achievements</a>
 
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                                                            <ul>
 
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                                                            <li><a href="https://2014.igem.org/Team:CU-Boulder/Abstract">Abstract</a></li><li>
 
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                                                            <a href="https://2014.igem.org/Team:CU-Boulder/Results">Results</a></li><li>
 
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                                                            <a href="https://2014.igem.org/Team:CU-Boulder/Biobricks">Biobricks</a></li><li>
 
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                                                            <a href="https://2014.igem.org/Team:CU-Boulder/Medal">Medal Requirements</a></li>
 
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                                                            </ul>
 
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                                                        </li><li>
 
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<a href="https://2014.igem.org/Team:CU-Boulder/Safety">Safety</a>
 
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                                                            <ul>
 
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                                                            <li><a href="https://2014.igem.org/Team:CU-Boulder/Ethics">Ethics</a></li><li>
 
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                                                            <a href="https://2014.igem.org/Team:CU-Boulder/ViralSafety">Viral Safety</a></li><li>
 
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                                                            <a href="https://2014.igem.org/Team:CU-Boulder/Outreach">Outreach</a></li><li>
 
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                                                            <a href="https://2014.igem.org/Team:CU-Boulder/LabSafety">In Lab Safety</a></li>
 
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                                                            </ul>
 
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<a href="https://2014.igem.org/Team:CU-Boulder/Team">Team</a></li>
 
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<h2 id="crispr"><span>CRISPR-Cas Mediated Phage Therapy</span></h2>
 
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                                        <p id="crispr" style="font-size: 18pt;">the Future Antibacterial Agent</p>
 
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<a href="#one" class="button style2 down">More</a>
 
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<h2>Issue</h2>
 
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</header>
 
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<p>In the last decade the number of antibiotic resistant bacteria has grown at
 
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a shocking rate, making these “superbugs” one of our top global health threats.
 
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This trend indicates that the golden age of antibiotics is ending and makes the
 
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search for new antibacterial treatments more important than ever. New bacterial
 
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treatments need the ability to adapt faster than the harmful bacteria that they
 
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target. Additionally, new treatments must preserve essential bacteria of the
 
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microbiome and specifically target pathogenic bacteria in a mixed population.</p>
 
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<h2>Technology</h2>
 
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<p>New technology has recently emerged that allows us to achieve these goals.
 
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CRISPR-Cas9 consists of an endonuclease (Cas9) that is guided to a specific
 
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sequence within a genome by a CRISPR RNA component. Once targeted to the
 
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genome, Cas9 causes a double stranded break, killing the host bacterial cell.
 
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Because the killing relies on the sequence of the CRISPR guide RNA, which can
 
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be engineered to contain a short specific nucleotide sequence, unique genes
 
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within any pathogenic bacteria can be targeted.</p>
 
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<h2>Our Project</h2>
 
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<p>Utilizing a non-replicating
 
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phage as a vector, we can efectively deliver the CRISPR-Cas9 machinery to cells
 
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and kill bacteria through CRISPR-Cas9–targeting of the genome. Ongoing
 
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experiments are aimed at demonstrating that sequence-specific killing can
 
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occur in a mixed population of cells as well as in an in vivo model. We believe
 
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that this technology, which we refer to as “Pathogen Assassin” will have broad
 
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applications ranging from medicine to industry and beyond.</p>
 
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Revision as of 02:42, 9 September 2014