Difference between revisions of "Team:Alverno CA/Experiment"
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<h5>Cultures that contained strains with plasmids with a 500bp spacer or 1000bp spacer, were diluted to normalize their OD absorbance. RFP expression (in AFU), GFP expression (in AFU), and OD was measured in a plate reader (<a href="http://www.perkinelmer.com/product/victor-x5-for-fl-lum-uv-trf-fp-2030-0050">VICTOR-X3</a>). For strains using a 1000bp spacer we the effects of using inducer (ATc and IPTG) were tested as well. (See our <a href="https://2016.igem.org/Team:Alverno_CA/Protocols">Plate Reading (for Fluorescence, Absorbance, Induction, etc.) Protocol</a> for more information) </h5> | <h5>Cultures that contained strains with plasmids with a 500bp spacer or 1000bp spacer, were diluted to normalize their OD absorbance. RFP expression (in AFU), GFP expression (in AFU), and OD was measured in a plate reader (<a href="http://www.perkinelmer.com/product/victor-x5-for-fl-lum-uv-trf-fp-2030-0050">VICTOR-X3</a>). For strains using a 1000bp spacer we the effects of using inducer (ATc and IPTG) were tested as well. (See our <a href="https://2016.igem.org/Team:Alverno_CA/Protocols">Plate Reading (for Fluorescence, Absorbance, Induction, etc.) Protocol</a> for more information) </h5> | ||
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<h3> Testing dCas9 clamps <i>in vitro</i> </h3> | <h3> Testing dCas9 clamps <i>in vitro</i> </h3> | ||
<h5> For cultures containing strains with plasmids that had a dCas9 clamp site spacer, cultures were mini-prepped to extract the plasmid DNA. In order to run our plasmids containing the dCas9 clamp site, we also had to design gRNA plasmids and obtain dCas9 expression plasmids (<a href="https://www.addgene.org/48657/">DS-SPCasN-</a>). All three of these plasmids were miniprepped and then expressed using TX-TL, an in vitro, prototyping technique which mimics cell environments for transcription and translation. For our first run we did not use inducer, but for our second run we used ATc and IPTG to induce the TetR and LacI promoters on the GFP and RFP devices, respectively. In the plate reader we obtained results that measured GFP and RFP expression. (see <a href="https://2016.igem.org/Team:Alverno_CA/Results">Results</a>) Once again, because the GFP and RFP devices were placed in different orientations we can observe whether or not supercoiling is present and whether or not it was reduced. (See our <a href="https://2016.igem.org/Team:Alverno_CA/Protocols">Plate Reading (for Fluorescence using TX-TL) Protocol</a> for more information)</h5> | <h5> For cultures containing strains with plasmids that had a dCas9 clamp site spacer, cultures were mini-prepped to extract the plasmid DNA. In order to run our plasmids containing the dCas9 clamp site, we also had to design gRNA plasmids and obtain dCas9 expression plasmids (<a href="https://www.addgene.org/48657/">DS-SPCasN-</a>). All three of these plasmids were miniprepped and then expressed using TX-TL, an in vitro, prototyping technique which mimics cell environments for transcription and translation. For our first run we did not use inducer, but for our second run we used ATc and IPTG to induce the TetR and LacI promoters on the GFP and RFP devices, respectively. In the plate reader we obtained results that measured GFP and RFP expression. (see <a href="https://2016.igem.org/Team:Alverno_CA/Results">Results</a>) Once again, because the GFP and RFP devices were placed in different orientations we can observe whether or not supercoiling is present and whether or not it was reduced. (See our <a href="https://2016.igem.org/Team:Alverno_CA/Protocols">Plate Reading (for Fluorescence using TX-TL) Protocol</a> for more information)</h5> | ||
Revision as of 02:48, 20 October 2016
Experiment
DVK_AE (derived from pSB1K3). In between the two genes on each plasmid, we placed one of several insulators to separate the genes. These included a 500bp spacer, a 1000 bp spacer, and a dCas9 clamp; each was designed to isolate and eliminate interference. Constructed plasmids were inserted into E. coli (DH5α). Ultimately, the goal of the experiment was to accurately demonstrate interference between two genes (RFP/GFP) on the same plasmid and, in addition, find an insulating mechanism to restrain the effects of possible supercoiling. (For more details, see Design)
After constructing these plasmids, we grew transformed E. coli as overnight liquid cultures.Methods
Testing spacers in vivo
Cultures that contained strains with plasmids with a 500bp spacer or 1000bp spacer, were diluted to normalize their OD absorbance. RFP expression (in AFU), GFP expression (in AFU), and OD was measured in a plate reader (VICTOR-X3). For strains using a 1000bp spacer we the effects of using inducer (ATc and IPTG) were tested as well. (See our Plate Reading (for Fluorescence, Absorbance, Induction, etc.) Protocol for more information)
Testing dCas9 clamps in vitro
For cultures containing strains with plasmids that had a dCas9 clamp site spacer, cultures were mini-prepped to extract the plasmid DNA. In order to run our plasmids containing the dCas9 clamp site, we also had to design gRNA plasmids and obtain dCas9 expression plasmids (DS-SPCasN-). All three of these plasmids were miniprepped and then expressed using TX-TL, an in vitro, prototyping technique which mimics cell environments for transcription and translation. For our first run we did not use inducer, but for our second run we used ATc and IPTG to induce the TetR and LacI promoters on the GFP and RFP devices, respectively. In the plate reader we obtained results that measured GFP and RFP expression. (see Results) Once again, because the GFP and RFP devices were placed in different orientations we can observe whether or not supercoiling is present and whether or not it was reduced. (See our Plate Reading (for Fluorescence using TX-TL) Protocol for more information)
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