Difference between revisions of "Team:Concordia"

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<h5> Combat Cells! </h5>
 
<h5> Combat Cells! </h5>
<p dir="ltr" style="line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt; text-indent: 36pt; text-align: justify;"><span id="docs-internal-guid-6f5269ce-5f9e-4027-3241-98d84929f978"><span style="font-size: 16px; font-family: 'Times New Roman'; color: rgb(0, 0, 0); vertical-align: baseline; white-space: pre-wrap;"> This year, Concordia University’s iGEM team aims to adapt the popular and engaging TV show Robot Wars, in which teams design and battle robots, and incorporate our spin for the synthetic biology community. Our project consists of equipping cells with nanoparticles and have them battle one another, with the intention of creating a broadcast acting as a medium through which we can entertain, educate, and inspire the public to participate in synthetic biology. The project involves three phases: nanoparticle synthesis, nanoparticle attachment, and analysis of cell survival on a microfluidic chip.  
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<p dir="ltr" style="line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt; text-indent: 36pt; text-align: justify;"><span id="docs-internal-guid-6f5269ce-5f9e-4027-3241-98d84929f978"><span style="font-size: 16px; font-family: 'Times New Roman'; color: rgb(0, 0, 0); vertical-align: baseline; white-space: pre-wrap;"> This year, our iGEM team representing Concordia University aims to design Combat Cells, a novel adaptation of the popular and engaging TV show ‘Robot Wars’. The project concept involves the design and battling of ‘cellular robots,’ providing a new spin on synthetic biology for the scientific community. Our project consists of equipping cells with nanoparticles and having them battle one another in a controllable microfluidic device. Through this, our intention is to  create and broadcast a web series through which we can entertain, educate, and inspire the public to participate in synthetic biology, and even create their own Combat Cells. The project encompasses  three phases: nanoparticle synthesis, nanoparticle attachment, and analysis of cell survival on a microfluidic chip.  
To generate nanoparticles, we are using plants such as garlic, aloe vera and cabbage. Plants possess a variety of biomolecules that are capable of reducing and stabilizing metal ions to their nanoparticle form. We can manipulate the sizes and shapes of nanoparticles by varying the amounts of plant extract and metallic solutions used. Then, using an AFM or TEM, we will characterize the nanoparticles synthesized. Here we aim to develop optimized methods for controlling the shapes and sizes of the nanoparticles using plant-mediated synthesis. Furthermore, incorporating this eco-friendly and cost-effective approach to synthesizing nanoparticles has allowed our project to reduce the amount of waste we produce, as well as reduce the amount of chemicals we expose to the environment.  
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We then want to develop an effective linkage method between the nanoparticles and the cell’s surface, for both bacterial and eukaryotic model systems. Additionally, we intend to study the relationship between nanoparticle abundance and localization on the protective qualities offered to the cell. After equipping the cells with nanoparticles, cellular opponents will be guided through an obstacle course leading to the battledome, designed on a microfluidics chip. The obstacle course will test the protective abilities of the nanoparticles against varying environmental conditions. Once the opposing species have reached the battledome, they will come into physical contact with each other. Here we will test the protective abilities of nanoparticles against other equipped species. Our aim here is to enhance nanoparticle-coated cell survival in different chemical conditions, and to examine the interactions occurring between coated cells.
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<b>Nanoparticle Synthesis</b>
All of this will occur within the controlled environment of a microfluidics chip, which we will design. Using microfluidics will allow us to dictate the mobility of the cells. Furthermore, experiments run through microfluidics require a small quantity of solutions, permitting us to further reduce the amount of waste we produce throughout our project. After the cell battle is finished, we will test the survival of the cells using pigments.  
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To generate nanoparticles, we are harnessing the reductive powers of plants such as garlic, aloe vera and cabbage. Plants possess a variety of biomolecules that are capable of reducing and stabilizing metal ions to form nanoparticles. The sizes and shapes of nanoparticles can be manipulated by varying the amounts of plant extract and metallic solutions used for synthesis. Using a Transmission Electron Microscope (TEM), the nanoparticles synthesized can further be characterized. In this we aim to develop optimized methods for controlling the shapes and sizes of the nanoparticles using plant-mediated synthesis. Furthermore, incorporating this eco-friendly and cost-effective approach to synthesizing nanoparticles will allow our project to reduce the amount of waste we may produce during nanoparticle synthesis.
Ultimately, we envision a multi-team league in which every team has a unique nanoparticle synthesis and attachment strategy. </p>
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Beyond this, other methods of nanoparticle synthesis are used known as chemical and recombinant synthesis. Martin and Turkevich methods are used for chemical nanoparticle synthesis. Martin uses the strong reducing power of sodium borohydride to reduce gold nuclei into small gold nanoparticles in the 3-6nm diameter range. The gold solution that is being reduced, also contains trisodium citrate whose ions will cap and stabilise the gold nanoparticles. The Turkevich method uses the moderate reducer and strong stabiliser trisodium citrate whose reducing power is increased by heating the solution containing silver nuclei. This reduction of silver nuclei would lead to formation of nanoparticles in the 40-60nm diameter range.  
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The recombinant method will involve the expression of the MelA gene, which will lead to the formation of eumelanin. This protein will in turn reduce the gold nuclei within E. coli cells and will intracellularly form gold nanoparticles. FhuA-GBP, a transmembrane protein linked to a gold-binding peptide, will be expressed in order to induce extracellular display of gold nanoparticles.
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<b>Nanoparticle Attachment</b>
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The next step following nanoparticle synthesis is nanoparticle-cell attachment. To do this, our team’s goal is to develop an effective linkage method between the nanoparticles and the cell’s surface, using both model organisms Escherichia coli and Saccharomyces cerevisiae. One of our methods includes the creation of a gold “Nanoshell” made from gold nanoparticles coated with L-cysteine surrounding the outer surface of yeast cells. Another one of our methods involves involves coating silver nanoparticles with polyelectrolytes and attaching these to the surface of both yeast and E. coli cells. We intend to study the relationship between nanoparticle abundance as well as localization on the protective qualities offered to the cell by nanoparticle cell coating.  
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 +
 
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<b>Battle on a Microfluidic Chip</b>
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Microfluidic chips with varying channel diameters will be designed using AutoCAD and printed onto photomasks which will act to transfer the generated pattern onto the chip. The customized chips will incorporate a battledome where two differently nanoparticle-coated cells will be forced to physically interact and ‘battle’. During this battle, the team will compare the relative protective abilities of the different nanoparticle coatings in order to determine which type of nanoparticle-cell combination is the ultimate winner! In parallel, the nanoparticle-coated cells in the microfluidic chip will be exposed to different physical and chemical “obstacles”  such as varied temperatures, salt concentrations, differing pH environments, and so forth, in order to test the protective abilities of the nanoparticles. The potential for colored pigments to travel through the cell membrane as a result of damage from the cell battle will be used to define a winner and a loser.
 +
 
 +
Ultimately, we envision a multi-team Combat Cells league in which every team has a unique nanoparticle synthesis method and attachment strategy that can be demonstrated through a entertaining webseries. It is our team’s hope that individuals of all ages and educational backgrounds will participate under the guidance of experienced coaches to develop novel strategies to design their own Combat Cells using innovative biotechnological approaches.
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<h5> Editing your wiki </h5>
 
<h5> Editing your wiki </h5>
 
<p>On this page you can document your project, introduce your team members, document your progress and share your iGEM experience with the rest of the world! </p>  
 
<p>On this page you can document your project, introduce your team members, document your progress and share your iGEM experience with the rest of the world! </p>  
<p> <a href="https://2016.igem.org/wiki/index.php?title=Team:Example&action=edit"> Click here to edit this page! </a></p>
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<p> <a href="https://2016.igem.org/wiki/index.php?title=Team:Example&action=edit"> </a>Use WikiTools - Edit in the black menu bar to edit this page</p>
  
 
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<h5> Uploading pictures and files </h5>
 
<h5> Uploading pictures and files </h5>
 
<p> You can upload your pictures and files to the iGEM 2016 server. Remember to keep all your pictures and files within your team's namespace or at least include your team's name in the file name. <br />
 
<p> You can upload your pictures and files to the iGEM 2016 server. Remember to keep all your pictures and files within your team's namespace or at least include your team's name in the file name. <br />
When you upload, set the "Destination Filename" to <code>Team:YourOfficialTeamName/NameOfFile.jpg</code>. (If you don't do this, someone else might upload a different file with the same "Destination Filename", and your file would be erased!)</p>
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When you upload, set the "Destination Filename" to <br><code>T--YourOfficialTeamName--NameOfFile.jpg</code>. (If you don't do this, someone else might upload a different file with the same "Destination Filename", and your file would be erased!)</p>
  
  

Revision as of 21:29, 30 June 2016

iGEM Concordia Wiki

iGEM Concordia 2016

Our team is based in Concordia University in Montreal, Canada

Combat Cells!

This year, our iGEM team representing Concordia University aims to design Combat Cells, a novel adaptation of the popular and engaging TV show ‘Robot Wars’. The project concept involves the design and battling of ‘cellular robots,’ providing a new spin on synthetic biology for the scientific community. Our project consists of equipping cells with nanoparticles and having them battle one another in a controllable microfluidic device. Through this, our intention is to create and broadcast a web series through which we can entertain, educate, and inspire the public to participate in synthetic biology, and even create their own Combat Cells. The project encompasses three phases: nanoparticle synthesis, nanoparticle attachment, and analysis of cell survival on a microfluidic chip. Nanoparticle Synthesis To generate nanoparticles, we are harnessing the reductive powers of plants such as garlic, aloe vera and cabbage. Plants possess a variety of biomolecules that are capable of reducing and stabilizing metal ions to form nanoparticles. The sizes and shapes of nanoparticles can be manipulated by varying the amounts of plant extract and metallic solutions used for synthesis. Using a Transmission Electron Microscope (TEM), the nanoparticles synthesized can further be characterized. In this we aim to develop optimized methods for controlling the shapes and sizes of the nanoparticles using plant-mediated synthesis. Furthermore, incorporating this eco-friendly and cost-effective approach to synthesizing nanoparticles will allow our project to reduce the amount of waste we may produce during nanoparticle synthesis. Beyond this, other methods of nanoparticle synthesis are used known as chemical and recombinant synthesis. Martin and Turkevich methods are used for chemical nanoparticle synthesis. Martin uses the strong reducing power of sodium borohydride to reduce gold nuclei into small gold nanoparticles in the 3-6nm diameter range. The gold solution that is being reduced, also contains trisodium citrate whose ions will cap and stabilise the gold nanoparticles. The Turkevich method uses the moderate reducer and strong stabiliser trisodium citrate whose reducing power is increased by heating the solution containing silver nuclei. This reduction of silver nuclei would lead to formation of nanoparticles in the 40-60nm diameter range. The recombinant method will involve the expression of the MelA gene, which will lead to the formation of eumelanin. This protein will in turn reduce the gold nuclei within E. coli cells and will intracellularly form gold nanoparticles. FhuA-GBP, a transmembrane protein linked to a gold-binding peptide, will be expressed in order to induce extracellular display of gold nanoparticles. Nanoparticle Attachment The next step following nanoparticle synthesis is nanoparticle-cell attachment. To do this, our team’s goal is to develop an effective linkage method between the nanoparticles and the cell’s surface, using both model organisms Escherichia coli and Saccharomyces cerevisiae. One of our methods includes the creation of a gold “Nanoshell” made from gold nanoparticles coated with L-cysteine surrounding the outer surface of yeast cells. Another one of our methods involves involves coating silver nanoparticles with polyelectrolytes and attaching these to the surface of both yeast and E. coli cells. We intend to study the relationship between nanoparticle abundance as well as localization on the protective qualities offered to the cell by nanoparticle cell coating. Battle on a Microfluidic Chip Microfluidic chips with varying channel diameters will be designed using AutoCAD and printed onto photomasks which will act to transfer the generated pattern onto the chip. The customized chips will incorporate a battledome where two differently nanoparticle-coated cells will be forced to physically interact and ‘battle’. During this battle, the team will compare the relative protective abilities of the different nanoparticle coatings in order to determine which type of nanoparticle-cell combination is the ultimate winner! In parallel, the nanoparticle-coated cells in the microfluidic chip will be exposed to different physical and chemical “obstacles” such as varied temperatures, salt concentrations, differing pH environments, and so forth, in order to test the protective abilities of the nanoparticles. The potential for colored pigments to travel through the cell membrane as a result of damage from the cell battle will be used to define a winner and a loser. Ultimately, we envision a multi-team Combat Cells league in which every team has a unique nanoparticle synthesis method and attachment strategy that can be demonstrated through a entertaining webseries. It is our team’s hope that individuals of all ages and educational backgrounds will participate under the guidance of experienced coaches to develop novel strategies to design their own Combat Cells using innovative biotechnological approaches.

Styling your wiki

You may style this page as you like or you can simply leave the style as it is. You can easily keep the styling and edit the content of these default wiki pages with your project information and completely fulfill the requirement to document your project.

While you may not win Best Wiki with this styling, your team is still eligible for all other awards. This default wiki meets the requirements, it improves navigability and ease of use for visitors, and you should not feel it is necessary to style beyond what has been provided.

Wiki template information

We have created these wiki template pages to help you get started and to help you think about how your team will be evaluated. You can find a list of all the pages tied to awards here at the Pages for awards link. You must edit these pages to be evaluated for medals and awards, but ultimately the design, layout, style and all other elements of your team wiki is up to you!

Editing your wiki

On this page you can document your project, introduce your team members, document your progress and share your iGEM experience with the rest of the world!

Use WikiTools - Edit in the black menu bar to edit this page

Tips

This wiki will be your team’s first interaction with the rest of the world, so here are a few tips to help you get started:

  • State your accomplishments! Tell people what you have achieved from the start.
  • Be clear about what you are doing and how you plan to do this.
  • You have a global audience! Consider the different backgrounds that your users come from.
  • Make sure information is easy to find; nothing should be more than 3 clicks away.
  • Avoid using very small fonts and low contrast colors; information should be easy to read.
  • Start documenting your project as early as possible; don’t leave anything to the last minute before the Wiki Freeze. For a complete list of deadlines visit the iGEM 2016 calendar
  • Have lots of fun!
Inspiration

You can also view other team wikis for inspiration! Here are some examples:

Uploading pictures and files

You can upload your pictures and files to the iGEM 2016 server. Remember to keep all your pictures and files within your team's namespace or at least include your team's name in the file name.
When you upload, set the "Destination Filename" to
T--YourOfficialTeamName--NameOfFile.jpg. (If you don't do this, someone else might upload a different file with the same "Destination Filename", and your file would be erased!)

UPLOAD FILES