Difference between revisions of "Part:BBa K211002:Experience"
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===HKUST2009 lab experience of BBa_K211002=== | ===HKUST2009 lab experience of BBa_K211002=== | ||
| − | HKUST team in 2009 has characterized the BBa_K211002 in the two experiments as shown below. This chimeric odorant sensing GPCR has been proven to localize to the budding yeast membrane and upon binding to diacetyl, triggers downstream signalling pathway. | + | HKUST team in 2009 has characterized the [https://parts.igem.org/Part:BBa_K211002 BBa_K211002] in the two experiments as shown below. This chimeric odorant sensing GPCR has been proven to localize to the budding yeast membrane and upon binding to diacetyl, triggers downstream signalling pathway. |
1.Membrane localization | 1.Membrane localization | ||
| − | (1)[[ | + | (1)[[protocol 1]] |
(2)results | (2)results | ||
Results: | Results: | ||
| − | Upon inducing by | + | Upon inducing by galactose for 45mins to 90mins, membrane localization of the chimeric receptor in budding yeast can be clearly observed. |
[[Image:GPF2.jpg]] | [[Image:GPF2.jpg]] | ||
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Results | Results | ||
| − | After being induced with galactose, the chimeric receptor is induced with its ligand diacetyl. From 0 to 4 hours, the cells sense the ligand and trigger the downstream | + | After being induced with galactose, the chimeric receptor is induced with its ligand diacetyl. From 0 to 4 hours, the cells sense the ligand and trigger the downstream mating response, leading to a cell cycle arrest at G1 phase. As a result, the DNA content is shifting towards the G1 non-replicated DNA content. |
[[Image:FACS.jpg]] | [[Image:FACS.jpg]] | ||
| − | + | Protocol 1: | |
Fluorescence microscopy visualization | Fluorescence microscopy visualization | ||
1. Grow yeast transformed cells containing appropriate plasmids in 5 ml SCM minus His & glucose at 30ºC overnight.. | 1. Grow yeast transformed cells containing appropriate plasmids in 5 ml SCM minus His & glucose at 30ºC overnight.. | ||
| Line 30: | Line 30: | ||
5. Use 2μl cells and visualize the cells in a fluorescency microscopy. | 5. Use 2μl cells and visualize the cells in a fluorescency microscopy. | ||
| − | + | Protocol 2: | |
FACS | FACS | ||
1. Transformed yeast cells were induced with galactose first for 1 hour. | 1. Transformed yeast cells were induced with galactose first for 1 hour. | ||
Revision as of 12:59, 19 October 2009
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HKUST2009 lab experience of BBa_K211002
HKUST team in 2009 has characterized the BBa_K211002 in the two experiments as shown below. This chimeric odorant sensing GPCR has been proven to localize to the budding yeast membrane and upon binding to diacetyl, triggers downstream signalling pathway.
1.Membrane localization (1)protocol 1 (2)results
Results:
Upon inducing by galactose for 45mins to 90mins, membrane localization of the chimeric receptor in budding yeast can be clearly observed.
2.Odorant sensing (1)protocal 2 (2)results
Results
After being induced with galactose, the chimeric receptor is induced with its ligand diacetyl. From 0 to 4 hours, the cells sense the ligand and trigger the downstream mating response, leading to a cell cycle arrest at G1 phase. As a result, the DNA content is shifting towards the G1 non-replicated DNA content.
Protocol 1: Fluorescence microscopy visualization 1. Grow yeast transformed cells containing appropriate plasmids in 5 ml SCM minus His & glucose at 30ºC overnight.. 2. Add galactose (to a conc.of 2%) at a cell density corresponding to an OD600 of a 10-fold dilution reaching 0.8. 3. Continue growing cells at 30ºC for 30min to 1.5hr. 4. At time 30min, 60min, 90min, use 1ml of cells, spin down and resuspend cells in 10μl ddH2O. 5. Use 2μl cells and visualize the cells in a fluorescency microscopy.
Protocol 2: FACS 1. Transformed yeast cells were induced with galactose first for 1 hour. 2. Yeasts after 1 hour, at OD600 = 0.8 were induced with diacetyle solution at 5mM. 3. Every 1.5 hour we need to collect samples for FACS analaysis,both control or experiment groups. 4. FACS standard method for sample preparation. 5. Gel pictual for results. 2.Using FACS standard method to
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