Difference between revisions of "Team:Michigan/Results"
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| − | <div class = "container"> <h1 style="text-align:center; font-size: 75px;"><font face= "Poiret One">Results</font></h1> | + | <div class = "container"> <h1 style="text-align:center; font-size: 75px;"><font face= "Poiret One">Results</font></h1><hr> |
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| − | + | <h1 style="text-align:center; font-size: 50px;"><font face= "Poiret One">Isolated LacZ from iGem part BBa_K564012</h2><br> | |
| + | <p style="text-align:center; font-size:20px;"><font face="verdana">We transformed a vector with LacZ from the registry for further cloning, we need this vector to produce another plasmid with an alpha deletion(M15 mutant).</font><br><hr></p> <img src="https://static.igem.org/mediawiki/2016/7/73/Isolated_LacZ_from_iGem_part_BBa_K564012.png" width="500" height="500" style="float:center"> | ||
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| − | <h1 style="text-align:center; font-size: 50px;"><font face= "Poiret One"> | + | <h1 style="text-align:center; font-size: 50px;"><font face= "Poiret One">Transferring LacZ into pET28</h2><br> |
| − | <p style="text-align:center; font-size:20px;"><font face="verdana"> | + | <p style="text-align:center; font-size:20px;"><font face="verdana"> In order to have a control for our cell-free expression system, we cloned LacZ into the protein expression plasmid to compare LacZ expression to expression of our system with and without the presence of its target protein. </font><br><hr></p> <img src="https://static.igem.org/mediawiki/2016/e/e8/Transferring_LacZ_into_pET28.png" width="500" height="500" style="float:center"> |
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| − | + | <h1 style="text-align:center; font-size: 50px;"><font face= "Poiret One">Creation of delta-M15 Mutant</h2><br> | |
| − | </font></p> | + | <p style="text-align:center; font-size:20px;"><font face="verdana"> Successfully deleted the alpha fragment in our Lacz plasmid, leaving only the omega fragment. The omega fragment complements the alpha fragment produced in the proximity-dependent ligation forming functional LacZ. This enzyme can break down X-Gal giving a colorimetric output. The plasmid is a very important part of our system, allowing alpha complementation and therefore producing a color visible to the naked eye. <br><br> |
| − | + | ||
| + | <a href="https://static.igem.org/mediawiki/2016/f/f8/Sequencing-Results-Using-T7-Primer-alignment_%281%29.pdf" target="_blank">Click to see sequencing results.</a></font><br></p> | ||
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| + | <h1 style="text-align:center; font-size: 50px;"><font face= "Poiret One">Proximity-Dependent Ligation Assay in Agarose Gel using SYBR Gold</h2><br> | ||
| + | <p style="text-align:center; font-size:20px;"><font face="verdana"> | ||
| + | Proximity dependent ligation allows our system to only be activated in the presence of its target protein. We decided to test our system using thrombin as a proof of concept.<br><br> | ||
| + | |||
| + | In this assay we aim to see the probes and connector ligated in the presence of thrombin, this should be about 300 base pairs long. In the absence of thrombin each component would just be floating in the solution unable to bind to each other, the probes are 145 and 163 base pairs long. Since we are trying to see the size of single stranded DNA bands, which can be difficult to visualize with ethidium bromide, we used SYBR Gold dye for staining. | ||
| + | <br><br> | ||
| + | We also wanted to test which connector binds the best out of three different length connectors, we set up three reactions without thrombin and three with thrombin, using different connectors, making a total of six reactions. Samples were left incubating at 35C for 9 hours and heated to 70C to deactivate ligase and melt the connector-probe interactions. | ||
| + | The first three lanes have the different sizes of connectors in ascending base pair length (going from left to right), no thrombin was added to the first three lines. The next three lanes are identical except they also contain thrombin. The last lane is probe 1 alone without any other reaction components added. The bands observed for probe 1 alone seem to suggest that two common conformations for probe 1, an unfolded conformation which is observed to run at approximately the position of the 100bp band on the ladder, and a folded conformation which runs farther down on the gel. The bands for the ligation reactions do not seem to show significant ligation activity, because there is no clear high molecular weight band; however, there may be a small amount of ligation occurring in lane 5, the reaction with the 3C connector and thrombin added, evidenced by the faint high molecular weight band in that lane. | ||
| + | </font><br><hr></p> <img src="https://static.igem.org/mediawiki/2016/8/8c/TestingPLAagarose.JPG" width="500" height="500" style="float:center"> | ||
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| − | <p style="text-align:center; font-size:20px;"><font face="verdana">We | + | Proximity-Dependent Ligation Assay (extended)</h2><br> |
| + | <p style="text-align:center; font-size:20px;"><font face="verdana"> We tested the proximity dependent ligation assay using a wider range of conditions, still using an agarose gel and SYBR Gold stain to visualize the DNA bands produced. In the first lane we use a 1kb plus ladder from Thermo Fisher. Lane 2 is a 30 minute reaction at room temperature without thrombin. Lane 3 is a 30 minute reaction at room temperature with thrombin added. Lanes 4 and 5 are the same as lanes 3 and 4 but run at 37 degrees C. Lane 6 is a 4 hour reaction at room temperature without thrombin. Lane 7 is a 4 hour reaction at room temperature with thrombin added. Lanes 8 and 9 are the same as lanes 6 and 7 but run at 37 degrees C. Lane 10 is a 19 hour reaction at room temperature without thrombin. Lane 11 is a 19 hour reaction at room temperature with thrombin added. Lanes 12 and 13 are the same as lanes 10 and 11 but run at 37 degrees C. The results do not seem to show any successful ligation. Interestingly, we see faint red bands of higher molecular weight in the 19 hour reactions which were run at 37 degrees C. </font><br><hr></p> | ||
| + | <img src="https://static.igem.org/mediawiki/2016/7/72/Prox-dep_assay_extended.JPG" width="500" height="500" style="float:center"><br> | ||
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Latest revision as of 03:41, 20 October 2016
Results
Isolated LacZ from iGem part BBa_K564012
We transformed a vector with LacZ from the registry for further cloning, we need this vector to produce another plasmid with an alpha deletion(M15 mutant).
Transferring LacZ into pET28
In order to have a control for our cell-free expression system, we cloned LacZ into the protein expression plasmid to compare LacZ expression to expression of our system with and without the presence of its target protein.
Creation of delta-M15 Mutant
Successfully deleted the alpha fragment in our Lacz plasmid, leaving only the omega fragment. The omega fragment complements the alpha fragment produced in the proximity-dependent ligation forming functional LacZ. This enzyme can break down X-Gal giving a colorimetric output. The plasmid is a very important part of our system, allowing alpha complementation and therefore producing a color visible to the naked eye.
Click to see sequencing results.
Click to see sequencing results.
Proximity-Dependent Ligation Assay in Agarose Gel using SYBR Gold
Proximity dependent ligation allows our system to only be activated in the presence of its target protein. We decided to test our system using thrombin as a proof of concept.
In this assay we aim to see the probes and connector ligated in the presence of thrombin, this should be about 300 base pairs long. In the absence of thrombin each component would just be floating in the solution unable to bind to each other, the probes are 145 and 163 base pairs long. Since we are trying to see the size of single stranded DNA bands, which can be difficult to visualize with ethidium bromide, we used SYBR Gold dye for staining.
We also wanted to test which connector binds the best out of three different length connectors, we set up three reactions without thrombin and three with thrombin, using different connectors, making a total of six reactions. Samples were left incubating at 35C for 9 hours and heated to 70C to deactivate ligase and melt the connector-probe interactions.
The first three lanes have the different sizes of connectors in ascending base pair length (going from left to right), no thrombin was added to the first three lines. The next three lanes are identical except they also contain thrombin. The last lane is probe 1 alone without any other reaction components added. The bands observed for probe 1 alone seem to suggest that two common conformations for probe 1, an unfolded conformation which is observed to run at approximately the position of the 100bp band on the ladder, and a folded conformation which runs farther down on the gel. The bands for the ligation reactions do not seem to show significant ligation activity, because there is no clear high molecular weight band; however, there may be a small amount of ligation occurring in lane 5, the reaction with the 3C connector and thrombin added, evidenced by the faint high molecular weight band in that lane.
In this assay we aim to see the probes and connector ligated in the presence of thrombin, this should be about 300 base pairs long. In the absence of thrombin each component would just be floating in the solution unable to bind to each other, the probes are 145 and 163 base pairs long. Since we are trying to see the size of single stranded DNA bands, which can be difficult to visualize with ethidium bromide, we used SYBR Gold dye for staining.
We also wanted to test which connector binds the best out of three different length connectors, we set up three reactions without thrombin and three with thrombin, using different connectors, making a total of six reactions. Samples were left incubating at 35C for 9 hours and heated to 70C to deactivate ligase and melt the connector-probe interactions. The first three lanes have the different sizes of connectors in ascending base pair length (going from left to right), no thrombin was added to the first three lines. The next three lanes are identical except they also contain thrombin. The last lane is probe 1 alone without any other reaction components added. The bands observed for probe 1 alone seem to suggest that two common conformations for probe 1, an unfolded conformation which is observed to run at approximately the position of the 100bp band on the ladder, and a folded conformation which runs farther down on the gel. The bands for the ligation reactions do not seem to show significant ligation activity, because there is no clear high molecular weight band; however, there may be a small amount of ligation occurring in lane 5, the reaction with the 3C connector and thrombin added, evidenced by the faint high molecular weight band in that lane.
