Difference between revisions of "Team:Vilnius-Lithuania/Public Engagement"

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         <p>As the idea of “DIY-science” workshop won lots of recognition and appreciation from the public, we want to share some <a href="">tutorials</a>, an open source <a href="">Arduino microcontroller operation code</a>, and a <a href="">principal scheme</a> of thermocycler device which might be helpful to invoke and improve this workshop idea among other iGEM teams in the near future.
 
         <p>As the idea of “DIY-science” workshop won lots of recognition and appreciation from the public, we want to share some <a href="">tutorials</a>, an open source <a href="">Arduino microcontroller operation code</a>, and a <a href="">principal scheme</a> of thermocycler device which might be helpful to invoke and improve this workshop idea among other iGEM teams in the near future.
 
         </p>
 
         </p>
   
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         <p><mark>EPE FOTO</mark></p>
        <h2>Applications</h2>
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        <p>The collaboration with the interdisciplinary artist and the opportunity to build and use homemade laboratory equipment brought us valuable insights about educating non-scientific people in noncommittal environment. We also noticed that workshop’s format allowed people to freely raise critical questions and sparked curiosity to carry out their own experiments. Since main principles of DIY biology were revealed, we showed the ability to perform experiments without extraordinary knowledge and convinced people that science can become a daily component of everyone’s routine.  
         <p>
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            <h5>Everyday lab work</h5>
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            <p>
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                A multi-plasmid system that is easy to assemble and control. With our framework the need to limit your
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                research to a particular plasmid copy number just because there are not enough right replicons to
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                choose from, is eliminated. With SynORI you can easily create a vector with a desired copy number that
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                suits your needs.</li>
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            </p>
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            <h5>Biological computing</h5>
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            <p>
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                The ability to choose a wide range of copy number options and their control types will make the
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                synthetic biology engineering much more flexible and predictable. Introduction of plasmid copy number
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                regulation is equivalent to adding a global parameter to a computer system. It enables the coordination
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                of multiple gene group expression.
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            </p>
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            <h5>Smart assembly of large protein complexes</h5>
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            <p>
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                The co-expression of multi-subunit complexes using different replicons brings incoherency to an already
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                chaotic cell system. This can be avoided by using SynORI, as in this framework every plasmid group uses
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                the same type of control, and in addition can act in a group-specific manner.</p>
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            <h5>Metabolic engineering</h5>
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            <p>
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                A big challenge for heterologous expression of multiple gene pathways is to accurately adjust the
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                levels of each enzyme to achieve optimal production efficiency. Precise promoter tuning in
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                transcriptional control and synthetic ribosome binding sites in translational control are already
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                widely used to maintain expression levels. In addition to current approaches, our framework allows a
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                simultaneous multiple gene control. Furthermore, an inducible regulation that we offer, can make the
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                search for perfect conditions a lot easier.
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            </p>
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         </p>
 
         </p>
         <p>
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         <p><mark>EPE VIDEO</mark></p>
        </p>
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        <p><mark>EPE PDF's</mark></p>
        <table style="width:100%">
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<thead>
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<td align='center'>Species sign in ODE system</td>
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<td align='center'>Species</td>
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<td align='center'>Initial concentration (M)</td>
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</thead>
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<tbody>
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<tr>
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<td align='center'>A</td>
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<td align='center'>pDNA+RNA I+RNAII early</td>
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<td align='center'>0</td>
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</tr>
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<tr>
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<td align='center'>B</td>
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<td align='center'>pDNA+RNA II short</td>
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<td align='center'>0</td>
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</tr>
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<tr>
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<td align='center'>RNAI</td>
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<td align='center'>RNA I</td>
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<td align='center'>1E-6</td>
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</tr>
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<tr>
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<td align='center'>D</td>
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<td align='center'>pDNA+RNA II long</td>
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<td align='center'>0</td>
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</tr>
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<tr>
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<td align='center'>E</td>
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<td align='center'>pDNA+RNAII primer</td>
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<td align='center'>0</td>
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</tr>
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<tr>
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<td align='center'>F</td>
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<td align='center'>RNA II long</td>
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<td align='center'>0</td>
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</tr>
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<tr>
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<td align='center'>G</td>
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<td align='center'>pDNA</td>
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<td align='center'>4E-8*</td>
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</tr>
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<tr>
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<td align='center'>H</td>
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<td align='center'>pDNA+RNA II+RNA I late</td>
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<td align='center'>0</td>
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</tr>
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<tr>
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<td align='center'>RNA II</td>
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<td align='center'>RNA II</td>
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<td align='center'>0</td>
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</tr>
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<tr>
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<td align='center'>J</td>
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<td align='center'>RNAI+RNAII</td>
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<td align='center'>0</td>
+
</tr>
+
</tbody>
+
</table>
+
 
     </div>
 
     </div>
 
</div>
 
</div>

Revision as of 17:24, 17 October 2018

Public Engagement

Description

With the intention to prove to the lay public that everyone has potential to become a scientist and that research does not necessarily require an advanced laboratory, we organized a unique and public “DIY-science” workshop. To make science more approachable, we performed PCR and gel electrophoresis exceptionally with homemade laboratory equipment. People were impressed that such a complicated-looking investigation could be done with virtually simple implementation. During the workshop many questions led to discussions about the limitations of DIY biology, biohacking, and homemade laboratories as well.

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