Abstract
The activities of many mammalian membrane proteins including G-protein coupled receptors are cholesterol-dependent. Unlike higher eukaryotes, yeast do not make cholesterol. Rather they make a related molecule called ergosterol. As cholesterol and ergosterol are biologically non-equivalent, the potential of yeast as hosts for overproducing mammalian membrane proteins has never been fully realised. To address this problem, we are trying to engineer a novel strain of Saccharomyces cerevisiae in which the cholesterol biosynthetic pathway of mammalian cells has been fully reconstituted. Thus far, we have created a modified strain that makes cholesterol-like sterols which has an increased capacity to make G-protein coupled receptors compared to control yeast.
Original language | English |
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Pages (from-to) | 287-292 |
Number of pages | 6 |
Journal | Methods |
Volume | 55 |
Issue number | 4 |
Early online date | 6 Oct 2011 |
DOIs | |
Publication status | Published - Dec 2011 |
Keywords
- cell membrane
- cholesterol
- molecular cloning
- genetic engineering
- humans
- genetically modified organisms
- G-protein-coupled receptors
- recombinant proteins
- saccharomyces cerevisiae
- sterols
- genetic transformation