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Protein Trafficking
Responsible for:
Target ACE proteins into mitochondria
Parts submitted: BBa_K1119000, BBa_K1119001 & BBa_K1119009
Team:Hong Kong HKUST/modules
From 2013.igem.org
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Revision as of 00:02, 28 September 2013
Project Outline
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!
Cell Viability & Fatty Acid Quantification
Responsible for:
Measuring cell viability at different fatty acid concentration & measure fatty acid uptake rate
Parts submitted: -
Fatty Acid Sensing Mechanism
Responsible for:
Introduce inducible system that allows tunable fatty acid uptake by sensing fatty acid concentration
Parts submitted: -
Glyoxylate Shunt
Responsible for:
Introduce glyoxylate enzymes responsible for the shunt
Parts submitted:BBa_K1119002, BBa_K1119003, BBa_K1119004, BBa_K1119006 & BBa_K1119008
