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+ | <div style="max-width:1000px; margin:0 auto; padding:0px 10px 10px 10px;"> | ||
+ | <div class="column full_size"> | ||
+ | <p>The results of the main experiments described on the <a href="/Team:Pittsburgh/Experiments" target="_blank">Experiments</a> page. For more details about our daily activities and experiments, visit our <a href="/Team:Pittsburgh/Notebook" target="_blank">Notebook</a>.</p></div> | ||
+ | |||
+ | <div class="table column full_size" style="padding-top:0;"> | ||
+ | <h2 style="padding-top:0;">Contents</h2> | ||
+ | <ul class="table"> | ||
+ | <li><a href="#cell-free" class="table">Cell-Free System</a></li> | ||
+ | <li><a href="#DNAzyme" class="table">DNAzyme</a></li> | ||
+ | <li><a href="#toehold" class="table">Toehold Switch</a></li> | ||
+ | <li><a href="#reporter" class="table">Reporter</a></li> | ||
+ | <li><a href="#amplifier" class="table">Amplifier</a></li> | ||
+ | |||
+ | </ul> | ||
+ | </div> | ||
+ | |||
+ | <div class="notebook column full_size"> | ||
+ | |||
+ | <span class="anchor" id="cell-free"></span> | ||
+ | <h1>Cell-Free System</h1> | ||
+ | <h2>Linear versus Plasmid DNA</h2> | ||
+ | <p>In <a href="/Team:Pittsburgh/Notebook#Week8" target="_blank">Week 8</a>, we found that linear DNA does not perform better than plasmid DNA in PURExpress. | ||
+ | <img src="https://static.igem.org/mediawiki/2016/b/b1/T--Pittsburgh--Results_LinPlasDNA.jpg" style="display:block;width:50;margin:auto;"> | ||
+ | However, a comparison by concentration of DNA instead of mass would be more accurate because the plasmid has much more "extra" DNA than the linear form. | ||
+ | </p> | ||
+ | <h2>Reaction Volume Reduction</h2> | ||
+ | <p>In <a href="/Team:Pittsburgh/Notebook#Week6" target="_blank">Week 6</a>, we ran cell-free reactions over a range of volumes. Each reaction contained 5 ng/μL of plasmid eGFP. As shown in the figure below, there was still a signal with a reaction volume of 5 μL. Thus, all our reactions are run at 5 μL. | ||
+ | <img src="https://static.igem.org/mediawiki/2016/d/d2/T--Pittsburgh--Results_RxnVolume.jpg" style="display:block;width:50;margin:auto;"> | ||
+ | </p> | ||
+ | <h2>Dilution</h2> | ||
+ | <p>After six hours of incubation in the plate reader, the diluted reactions did not turn purple. However, after leaving them in the incubator overnight, the reactions darkened in color. The time course data shown below is more a function of evaporation than reaction progress; the liquid evaporated over the course of the run. | ||
+ | <img src="https://static.igem.org/mediawiki/2016/3/36/T--Pittsburgh--Results_TimeCourse.jpg" style="display:block;width:50;margin:auto;"> | ||
+ | </p> | ||
+ | |||
+ | <a href="#Top">Back to Top</a> | ||
+ | |||
+ | <span class="anchor" id="DNAzyme"></span> | ||
+ | <h1>DNAzyme</h1> | ||
+ | <h2>Substrate Sequestration</h2> | ||
+ | <p>The thallium DNAzyme was annealed at ratios of substrate to catalytic strand varying from 1:1 to 1:500. The gel below suggests that all of the substrate strand is sequestered, but the thickness of the catalytic strand's band as the ratio increases could be blocking the signal from the substrate strand. However, the duplex did not activate the toehold switch. | ||
+ | <img src="https://static.igem.org/mediawiki/2016/6/6d/T--Pittsburgh--Results_Sequestration.jpg" style="display:block;width:50;margin:auto;"> | ||
+ | </p> | ||
+ | <h2>Hairpin versus Duplex</h2> | ||
+ | <p>In cell-free extract, the lead hairpin DNAzyme produces higher activation of the toehold switch than the duplex DNAzyme in a 1:1000 ratio. This could be a result of the excess catalytic strand interfering with the other processes occurring in the reaction. | ||
+ | <img src="https://static.igem.org/mediawiki/2016/6/68/T--Pittsburgh--Results_hairpin.jpg" style="display:block;width:50;margin:auto;"> | ||
+ | </p> | ||
+ | <h2>Cleavage</h2> | ||
+ | <p>Although the dPAGE assays do not provide clear information, the cell-free reactions (such as the one whose results are shown above) suggest that the DNAzyme does cleave its substrate.</p> | ||
+ | |||
+ | <a href="#Top">Back to Top</a> | ||
+ | |||
+ | <span class="anchor" id="toehold"></span> | ||
+ | <h1>Toehold Switch</h1> | ||
+ | <h2>RNA Trigger</h2> | ||
+ | <p>As shown below, the plasmid triggers activate the toehold switch with as little as 10 ng of plasmid in a 25-μL reaction. [comparison to Collins] | ||
+ | <img src="https://static.igem.org/mediawiki/2016/d/da/T--Pittsburgh--Results_RNAtrig.jpg" style="display:block;width:50;margin:auto;"> | ||
+ | </p> | ||
+ | <h3>DNA Trigger</h3> | ||
+ | <p>The DNA trigger also activated the toehold switch at concentrations as low as 1.0 pM. The toehold switch also displays a dosage response. In addition, the triggers are switch-specific--the trigger for the D switch does not activate the G switch. | ||
+ | <img src="https://static.igem.org/mediawiki/2016/5/57/T--Pittsburgh--Results_DNAtrig.jpg" style="display:block;width:50;margin:auto;"> | ||
+ | </p> | ||
+ | <h3>Sequestered DNA Trigger</h3> | ||
+ | <p>As shown in the results for the Hairpin versus Duplex experiment above, the duplex and folded hairpin do not activate the toehold switch because the trigger is hybridized to the catalytic strand.</p> | ||
+ | <a href="#Top">Back to Top</a> | ||
+ | |||
+ | <span class="anchor" id="reporter"></span> | ||
+ | <h1>Reporter</h1> | ||
+ | <h2>amilCP</h2> | ||
+ | <p>Results from sequencing in <a href="/Team:Pittsburgh/Notebook#Week11" target="_blank">Week 11</a> suggest that our completed construct contains CFP instead of amilCP. No color was detected in T7 cells or in cell-free reactions.</p> | ||
+ | <h2>LacZ</h2> | ||
+ | <p>how'd mutagenesis go?</p> | ||
+ | <a href="#Top">Back to Top</a> | ||
+ | |||
+ | <span class="anchor" id="amplifier"></span> | ||
+ | <h1>Amplifier</h1> | ||
+ | <p>assembled in week 14, sequencing results?</p> | ||
+ | <a href="#Top">Back to Top</a> | ||
+ | |||
+ | |||
+ | </div> | ||
+ | </div> | ||
+ | |||
+ | |||
+ | <h2>RNA Trigger</h2> | ||
+ | <p>In <a href="https://2016.igem.org/Team:Pittsburgh/Notebook#Week5" target="_blank">Week 5</a>, we showed that LacZ is expressed when the plasmids for the switch and trigger constructs are combined in a cell-free system.</p> | ||
+ | <h3>DNA Trigger</h3> | ||
+ | <p>In <a href="https://2016.igem.org/Team:Pittsburgh/Notebook#Week6" target="_blank">Week 6</a>, we showed that toehold switches are activated by single-stranded DNA triggers, but activation levels are lower than with RNA triggers.</p> | ||
+ | <h3>Sequestered DNA Trigger</h3> | ||
+ | <p>In <a href="https://2016.igem.org/Team:Pittsburgh/Notebook#Week7" target="_blank">Week 7</a>, we showed that single-stranded DNA triggers do not activate toehold switches if they are part of a hybridized complex.</p> | ||
+ | <a href="#Top">Back to Top</a> | ||
+ | |||
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Revision as of 21:52, 4 September 2016
Contact Us
The results of the main experiments described on the Experiments page. For more details about our daily activities and experiments, visit our Notebook.
Cell-Free System
Linear versus Plasmid DNA
In Week 8, we found that linear DNA does not perform better than plasmid DNA in PURExpress. However, a comparison by concentration of DNA instead of mass would be more accurate because the plasmid has much more "extra" DNA than the linear form.
Reaction Volume Reduction
In Week 6, we ran cell-free reactions over a range of volumes. Each reaction contained 5 ng/μL of plasmid eGFP. As shown in the figure below, there was still a signal with a reaction volume of 5 μL. Thus, all our reactions are run at 5 μL.
Dilution
After six hours of incubation in the plate reader, the diluted reactions did not turn purple. However, after leaving them in the incubator overnight, the reactions darkened in color. The time course data shown below is more a function of evaporation than reaction progress; the liquid evaporated over the course of the run.
Back to TopDNAzyme
Substrate Sequestration
The thallium DNAzyme was annealed at ratios of substrate to catalytic strand varying from 1:1 to 1:500. The gel below suggests that all of the substrate strand is sequestered, but the thickness of the catalytic strand's band as the ratio increases could be blocking the signal from the substrate strand. However, the duplex did not activate the toehold switch.
Hairpin versus Duplex
In cell-free extract, the lead hairpin DNAzyme produces higher activation of the toehold switch than the duplex DNAzyme in a 1:1000 ratio. This could be a result of the excess catalytic strand interfering with the other processes occurring in the reaction.
Cleavage
Although the dPAGE assays do not provide clear information, the cell-free reactions (such as the one whose results are shown above) suggest that the DNAzyme does cleave its substrate.
Back to TopToehold Switch
RNA Trigger
As shown below, the plasmid triggers activate the toehold switch with as little as 10 ng of plasmid in a 25-μL reaction. [comparison to Collins]
DNA Trigger
The DNA trigger also activated the toehold switch at concentrations as low as 1.0 pM. The toehold switch also displays a dosage response. In addition, the triggers are switch-specific--the trigger for the D switch does not activate the G switch.
Sequestered DNA Trigger
As shown in the results for the Hairpin versus Duplex experiment above, the duplex and folded hairpin do not activate the toehold switch because the trigger is hybridized to the catalytic strand.
Back to TopReporter
amilCP
Results from sequencing in Week 11 suggest that our completed construct contains CFP instead of amilCP. No color was detected in T7 cells or in cell-free reactions.
LacZ
how'd mutagenesis go?
Back to TopAmplifier
assembled in week 14, sequencing results?
Back to TopRNA Trigger
In Week 5, we showed that LacZ is expressed when the plasmids for the switch and trigger constructs are combined in a cell-free system.
DNA Trigger
In Week 6, we showed that toehold switches are activated by single-stranded DNA triggers, but activation levels are lower than with RNA triggers.
Sequestered DNA Trigger
In Week 7, we showed that single-stranded DNA triggers do not activate toehold switches if they are part of a hybridized complex.
Back to Top