Difference between revisions of "Team:Uppsala"

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                     <h2>Project Outline</h2>
 
                     <h2>Project Outline</h2>
 
                      
 
                      
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                    <!--------WORM CULTURING--------->
 
                     <h3><b>1. </b><a href="https://2018.igem.org/Team:Uppsala/Worm_Culturing"> Worm Culturing </a></h3>
 
                     <h3><b>1. </b><a href="https://2018.igem.org/Team:Uppsala/Worm_Culturing"> Worm Culturing </a></h3>
                    <p>The first step was to obtain live nematodes by the recovery of the eggs from the feces. After this process the large strongyles were divided from the small strongyles using a 3D printed microfluidic chip or a microscope and stored for successive use.</p><br>
 
                    <img class="content-card-img" src="https://static.igem.org/mediawiki/2018/archive/2/29/20180628152540%21T--Uppsala--Poop_culture.svg">
 
                    <p><b>Figure 1:</b>Flowchart representing the worm culturing outline.</p>
 
 
                      
 
                      
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                            <!-- Here you put your paragraphs -->
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                            <p><b>-</b> The first step was to obtain live nematodes by the recovery of the eggs from the feces. After this process the large strongyles were divided from the small strongyles using a 3D printed microfluidic chip or a microscope and stored for successive use.<br><br><b>Figure 1:</b>Flowchart representing the worm culturing outline.</p>
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                            <br>
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                        </div>
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                        <div class="side-img" style="background-color:darkolivegreen;">
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                          <!-- Here goes the big image to the right -->
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                          <img src="https://static.igem.org/mediawiki/2018/archive/2/29/20180628152540%21T--Uppsala--Poop_culture.sv"> 
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                        </div>
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                    </div>
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                    <!---------TRANSCRIPTOMIC + PHAGE DISPLAY------>
 
                      
 
                      
 
                     <h3><b>2. </b><a href="https://2018.igem.org/Team:Uppsala/Transcriptomics" >Transcriptomics</a> + <a href="https://2018.igem.org/Team:Uppsala/Phage_Display" >Phage Display</a></h3>
 
                     <h3><b>2. </b><a href="https://2018.igem.org/Team:Uppsala/Transcriptomics" >Transcriptomics</a> + <a href="https://2018.igem.org/Team:Uppsala/Phage_Display" >Phage Display</a></h3>
 
                     <p>As not a lot is known about our worms of interest, we needed an approach that would allow us to detect the worm without knowing its specific markers. For this, we developed new applications of two existing approaches.</p><br><br>
 
                     <p>As not a lot is known about our worms of interest, we needed an approach that would allow us to detect the worm without knowing its specific markers. For this, we developed new applications of two existing approaches.</p><br><br>
 
                      
 
                      
                     <ul><li><b>-</b> For the first one, we have been developing a custom transcriptomic analysis protocol. This was necessary because transcriptomics is a new application for Oxford Nanopore technology. The transcriptomics procedure relies on the co-culturing of nematodes with E.coli and subsequent sequencing of the bacterial mRNA. This will ideally reveal which genes are upregulated when the worm is next to the nematode. The promoters of these genes can then be used to develop a biosensor by linking them to a reporter!  
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                     As our result show, transcriptomics with the nanopore MinIon works if a better technique to reduce the amount of RNA in the sample is discovered thus we have discovered a new application to Oxford Nanopore Technology.
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                        <img class="content-card-img" src="https://static.igem.org/mediawiki/2018/5/5d/T--Uppsala--transcriptomics_flowchart.svg"><br>
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                    <!------LIST START------>
                        <p><b>Figure 2: </b>Flowchart representing the trancsriptomics outline.</p></li><br>
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                        <h4>Transcriptomics</h4></div>
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                    <div class="content-card pic-next-to-text">
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                        <div class="side-text">
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                            <!-- Here you put your paragraphs -->
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                            <p><b>-</b> For the first one, we have been developing a custom transcriptomic analysis protocol. This was necessary because transcriptomics is a new application for Oxford Nanopore technology. The transcriptomics procedure relies on the co-culturing of nematodes with E.coli and subsequent sequencing of the bacterial mRNA. This will ideally reveal which genes are upregulated when the worm is next to the nematode. The promoters of these genes can then be used to develop a biosensor by linking them to a reporter!  
 +
                     As our result show, transcriptomics with the nanopore MinIon works if a better technique to reduce the amount of RNA in the sample is discovered thus we have discovered a new application to Oxford Nanopore Technology.<br><br><b>Figure 2: </b>Flowchart representing the trancsriptomics outline.</p>
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                            <br>
  
                     <li><b>-</b>  
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                        </div>
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                        <div class="side-img" style="background-color:darkolivegreen;">
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                          <!-- Here goes the big image to the right -->
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                          <img src="https://static.igem.org/mediawiki/2018/5/5d/T--Uppsala--transcriptomics_flowchart.svg"> 
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                        </div>
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                        <!----------PHAGE DISPLAY------->
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                         <h4>Can remove heading if this will bein the middle of the page.</h4></div>
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                         <h4>Phage Display</h4></div>
 
                     <div class="content-card pic-next-to-text">
 
                     <div class="content-card pic-next-to-text">
 
                         <div class="side-text">
 
                         <div class="side-text">
 
                             <!-- Here you put your paragraphs -->  
 
                             <!-- Here you put your paragraphs -->  
                             <p>The second approach used a technique called “Phage Display”, which utilizes a random peptide library expressed on the surface of phages. By repeated rounds of affinity screening, only phages with high affinity to the molecule of interest will be selected. Sequencing the genetic information of these phages has allowed us to construct multiple peptide suggestions that may bind to our nematodes’ surface proteins.  This would allow the biosensor to aggregate at the detection sites and create a stronger signal. <br><br>
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                             <p><b>-</b> The second approach used a technique called “Phage Display”, which utilizes a random peptide library expressed on the surface of phages. By repeated rounds of affinity screening, only phages with high affinity to the molecule of interest will be selected. Sequencing the genetic information of these phages has allowed us to construct multiple peptide suggestions that may bind to our nematodes’ surface proteins.  This would allow the biosensor to aggregate at the detection sites and create a stronger signal. <br><br>
 
                             In our project, phage display has been used in a whole new way. Performing phage display on a whole organism is an unconventional and unpublished procedure. By creating a working protocol for the purpose of finding a specific binder for strongyles we have applied this Nobel-prize winning method in a new way.<br><br><b>Figure 3: </b>Flowchart representing the phage display outline.</p>
 
                             In our project, phage display has been used in a whole new way. Performing phage display on a whole organism is an unconventional and unpublished procedure. By creating a working protocol for the purpose of finding a specific binder for strongyles we have applied this Nobel-prize winning method in a new way.<br><br><b>Figure 3: </b>Flowchart representing the phage display outline.</p>
 
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                     <!-------REPORTER SYSTEM------->
  
 
                      
 
                      
 
                     <h3><b>3. </b><a href="https://2018.igem.org/Team:Uppsala/Reporter_System" >Reporter System</a></h3>
 
                     <h3><b>3. </b><a href="https://2018.igem.org/Team:Uppsala/Reporter_System" >Reporter System</a></h3>
                     <p>After receiving the results from either the transcriptomics or the phage display, they need to be combined with a reported to get a functioning diagnostic tool (Worm Buster).  We have adapted and troubleshot the expression of a fluorescent chromoprotein, UnaG, to be able to detect our worms in both the intestines and in feces. This would enable a relatively simple and quantitative way for ranchers to detect the worms of interest, using a cheap UV lamp, a dark room, and a camera!<br><br>
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                     In order to make this a viable reporter system, we wanted to make sure the original biobrick part was functional.  We show how we tweaked this part in order to study if it works properly so that it could be potentially used in future studies. </p>
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                    <img class="https://static.igem.org/mediawiki/2018/f/f5/T--Uppsala--AntennaPoop.svg">
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                    <p><b>Figure 4: </b>We would be able to detect the wormd in feces with this method.</p>
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                    <div class="card-holder">
           
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                    <div class="content-card pic-next-to-text">
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                        <div class="side-text">
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                            <!-- Here you put your paragraphs -->
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                            <p><b>-</b> After receiving the results from either the transcriptomics or the phage display, they need to be combined with a reported to get a functioning diagnostic tool (Worm Buster).  We have adapted and troubleshot the expression of a fluorescent chromoprotein, UnaG, to be able to detect our worms in both the intestines and in feces. This would enable a relatively simple and quantitative way for ranchers to detect the worms of interest, using a cheap UV lamp, a dark room, and a camera!<br><br>
 +
                     In order to make this a viable reporter system, we wanted to make sure the original biobrick part was functional.  We show how we tweaked this part in order to study if it works properly so that it could be potentially used in future studies.<br><br><b>Figure 4: </b>We would be able to detect the wormd in feces with this method.</p>
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                            <br>
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                        </div>
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                        <div class="side-img" style="background-color:darkolivegreen;">
 +
                          <!-- Here goes the big image to the right -->
 +
                          <img src="https://static.igem.org/mediawiki/2018/f/f5/T--Uppsala--AntennaPoop.svg">  
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                        </div>
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                    <!----------MODELING----------->
 
                     <h3><b>4. </b><a href="https://2018.igem.org/Team:Uppsala/Model" >Modeling</a></h3>
 
                     <h3><b>4. </b><a href="https://2018.igem.org/Team:Uppsala/Model" >Modeling</a></h3>
 
                         <h4>Optimization of the Time Between Treatments</h4>
 
                         <h4>Optimization of the Time Between Treatments</h4>

Revision as of 11:46, 16 October 2018




Uppsala iGEM 2018