Protein Trafficking
Responsible for:
Target ACE proteins into mitochondria
Parts submitted: BBa_K1119000, BBa_K1119001 & BBa_K1119009
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- | <br><br><br><div id="slide"><h3 class="title">Project Outline</h3><p id="isi"> | + | |
+ | <br><br><br><div id="slide"><h3 class="title">Project Outline</h3><p id="isi">Our ultimate goal is to build a ‘smart’ glyoxylate shunt that burns extra fatty acid when there is energy surplus. To achieve this, we would have to first build the shunt itself in mammalian cells. The shunt comprises two bacterial glyoxylate enzymes, isocitrate lyase (AceA) and malate synthase (AceB). Tagged with a localization signal peptide, they could be directed to the mitochondria and act on the citric acid cycle, eventually increasing fatty acid uptake. The two enzymes would be initially driven by constitutive promoters (CMV and EF-1alpha promoters), placing the shunt in a constantly “ON” state and burning calories regardless of the energy profile. To improve this, we are developing fatty acid responsive promoters, which, when used to regulate the glyoxylate enzymes, should dispense energy only when it is in excess. <strong>Hover</strong> your mouse and <strong>click</strong> on the images below to learn more about each modules!</p></div> | ||
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<div id="projinteract"></div> | <div id="projinteract"></div> | ||
- | <div id=" | + | <div id="article2" class="info1"><h3 class="kotak">Glyoxylate Shunt</h3><p><b><i>Responsible for:</b></i><br>Introduce glyoxylate enzymes responsible for the shunt<br><b><i>Parts submitted:</b></i><a href="http://parts.igem.org/Part:BBa_K1119002">BBa_K1119002</a>, <a href="http://parts.igem.org/Part:BBa_K1119003">BBa_K1119003</a>, <a href="http://parts.igem.org/Part:BBa_K1119006">BBa_K1119006</a>, <a href="http://parts.igem.org/Part:BBa_K1119008">BBa_K1119008</a>, <a href="http://parts.igem.org/Part:BBa_K1119010">BBa_K1119010</a> & <a href="http://parts.igem.org/Part:BBa_K1119006">BBa_K1119011</a></p></div> |
- | < | + | <div id="article" class="info1"><h3 class="kotak">Protein Trafficking</h3><p><b><i>Responsible for:</b></i><br>Target ACE proteins into mitochondria<br><b><i>Parts submitted:</b></i> <a href="http://parts.igem.org/Part:BBa_K1119000">BBa_K1119000</a>, <a href="http://parts.igem.org/Part:BBa_K1119001">BBa_K1119001</a> & <a href="http://parts.igem.org/Part:BBa_K1119009">BBa_K1119009</a></p></div> |
- | <div id="article"><h3 class="kotak">Protein Trafficking</h3><p><b><i>Responsible for:</b></i><br>Target ACE proteins into mitochondria<br><b><i>Parts submitted:</b></i> <a href="http://parts.igem.org/Part:BBa_K1119000">BBa_K1119000</a>, <a href="http://parts.igem.org/Part:BBa_K1119001">BBa_K1119001</a> & <a href="http://parts.igem.org/Part:BBa_K1119009">BBa_K1119009</a></p></div> | + | <div id="presentation" class="info1"><h3 class="kotak">Fatty Acid Sensing Mechanism</h3><p><b><i>Responsible for:</b></i><br>Introduce inducible system that allows tunable fatty acid uptake by sensing fatty acid concentration<br><b><i>Parts submitted:</b> - </i></p></div> |
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Our ultimate goal is to build a ‘smart’ glyoxylate shunt that burns extra fatty acid when there is energy surplus. To achieve this, we would have to first build the shunt itself in mammalian cells. The shunt comprises two bacterial glyoxylate enzymes, isocitrate lyase (AceA) and malate synthase (AceB). Tagged with a localization signal peptide, they could be directed to the mitochondria and act on the citric acid cycle, eventually increasing fatty acid uptake. The two enzymes would be initially driven by constitutive promoters (CMV and EF-1alpha promoters), placing the shunt in a constantly “ON” state and burning calories regardless of the energy profile. To improve this, we are developing fatty acid responsive promoters, which, when used to regulate the glyoxylate enzymes, should dispense energy only when it is in excess. Hover your mouse and click on the images below to learn more about each modules!
Responsible for:
Introduce glyoxylate enzymes responsible for the shunt
Parts submitted:BBa_K1119002, BBa_K1119003, BBa_K1119006, BBa_K1119008, BBa_K1119010 & BBa_K1119011
Responsible for:
Target ACE proteins into mitochondria
Parts submitted: BBa_K1119000, BBa_K1119001 & BBa_K1119009
Responsible for:
Introduce inducible system that allows tunable fatty acid uptake by sensing fatty acid concentration
Parts submitted: -