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2. Confirming the CFP sequence is functional
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<p>As part of the experiments to repair the CUP1p - [MS2-CFP] construct we need to determine if the CFP sequence used is functional or not. By confirming that the CFP protein is functional we can narrow down where the fault lies in the construct. If the CFP sequence was not functional this could mean that the construct was expressing properly but we simply could not detect this.</p> | <p>As part of the experiments to repair the CUP1p - [MS2-CFP] construct we need to determine if the CFP sequence used is functional or not. By confirming that the CFP protein is functional we can narrow down where the fault lies in the construct. If the CFP sequence was not functional this could mean that the construct was expressing properly but we simply could not detect this.</p> | ||
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We can conclude from this experiment that the reason we are not seeing any CFP expression in pRS414 is because the CFP protein is not being produced properly.</p> | We can conclude from this experiment that the reason we are not seeing any CFP expression in pRS414 is because the CFP protein is not being produced properly.</p> | ||
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Latest revision as of 11:54, 26 October 2010
University of Aberdeen - ayeSwitch
Confirming Functionality of CFP Sequence
Aim
As part of the experiments to repair the CUP1p - [MS2-CFP] construct we need to determine if the CFP sequence used is functional or not. By confirming that the CFP protein is functional we can narrow down where the fault lies in the construct. If the CFP sequence was not functional this could mean that the construct was expressing properly but we simply could not detect this.
Hypothesis
The CFP sequence is accurate and the reason why no expression of CFP is being observed is because the protein is not being synthesised properly or not all.
Protocol
The TEF1p -[CFP] plasmid has been used to drive the expression of fluorescent proteins. The TEF1 promoter has been shown to constitutively express GFP at high levels.
A restriction digest was performed using the enzymes Nde1 and Xba1 in order to remove GFP from the construct. The CFP sequence in CUP1p - [MS2-CFP] was then PCR amplified using primers to generate complementary overhangs to allow homologous recombination into the gaped TEF1p -[CFP] vector.
The gapped vector and the PCR product were co-transformed into yeast (BY4741ΔTrp strain) and incubated for several days. The resulting transformants were then cultured overnight in SD medium. Sample were washed and re-suspended in PBS and then observed under a microscope fitted with CFP filters.
Results
We can see from Fig.3 that the CFP protein is being properly expressed. This means that the sequence used for CFP in the CUP1p - [MS2-CFP] construct is accurate and should be working. During this experiment the sequence of MS2-CFP was also checked to ensure that during the design both proteins had remained in frame.
We can conclude from this experiment that the reason we are not seeing any CFP expression in pRS414 is because the CFP protein is not being produced properly.
 Return to Troubleshooting the CUP1p-[MS2-CFP] construct
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Return to Results Main Page
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