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 |
|---|---|
| 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