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Revision as of 23:52, 27 October 2012 by Yuichi Nishiwaki (talk | contribs) (Finding New Aptamers for New and Different Substrates)
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<li class="toppage"><a href="/wiki/Biomod/2012/UTokyo/UT-Hongo">Top</a></li> <li class="motives"><a href="/wiki/Biomod/2012/UTokyo/UT-Hongo/Intro">Motives</a></li> <!-- <li class="design"><a href="/wiki/Biomod/2012/UTokyo/UT-Hongo/Function">Design</a></li> --> <li class="result"><a href="/wiki/Biomod/2012/UTokyo/UT-Hongo/Assembly">Design & Results</a> <ul class="submenu"> <li><a href="/wiki/Biomod/2012/UTokyo/UT-Hongo/Assembly#Assembly_of_the_DNA_Shell">Assembly of the DNA Shell</a></li> <li><a href="/wiki/Biomod/2012/UTokyo/UT-Hongo/Assembly#Capturing_ability">Capturing Ability</a></li> <li><a href="/wiki/Biomod/2012/UTokyo/UT-Hongo/Assembly#Immobilizing_on_microfluidic_device">Immobilizing on microfluidic device</a></li> <li><a href="/wiki/Biomod/2012/UTokyo/UT-Hongo/Assembly#Supporting_Enzyme">Supporting Enzyme</a></li> </ul> </li> <li class="method"><a href="/wiki/Biomod/2012/UTokyo/UT-Hongo/Method">Method</a></li> <li class="futurework"><a href="/wiki/Biomod/2012/UTokyo/UT-Hongo/FutureWork">Progress & Beyond</a></li> <li class="team"><a href="/wiki/Biomod/2012/UTokyo/UT-Hongo/Team">Team</a></li> <li class="acknowledgement"><a href="/wiki/Biomod/2012/UTokyo/UT-Hongo/Acknowledgement">Acknowledgement</a></li>


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Progress of Our Research

We gave set the goal as below.

  1. Realize the DNA shell structure
  2. Confirm the three possible functionalities through experiments

After we had finished the experiments, assessment of how well we did was made.

Goal 1
Not only was the building of the DNA shell confirmed using the AFM but also the captured state was analysed geometrically. Therefore, we think that this goal was fully accomplished.
Goal 2.
As for the detection, we were able to confirm that by using more than one pair of fluorescent and quencher molecules, we were able to get a higher signal of the capturing. We also confirmed in the experiment of using DNA Shell to protect the HRP-Streptavidin that the activity of streptavidin could be retained even if it was in a captured state. Finally, the experiments showed that the attachment of DNA shell to the microfluidics device was also achieved.


To improve and give a more useful result to verify our idea, these experiments below should be conducted.

Finding the length of each fluorescent and quencher molecules where self-absorption does not occur
When we added 12 equiv. pairs of fluorescent and quencher molecules, there was no difference in the change in fluorescence. This is thought to be caused by a phenomena called self-absorption, where the emitted fluorescence is captured by another fluorescent molecule. This can be prevented by enlarging the distance between the fluorescent molecules. Finding the length this phenomena will not be troubling would be a method to make this more device useful.
Protection experiment using new Trypsin reagent and also with different groups of proteases
Our experiment with Trypsin seemed not to work because of the failure in Trypsin activity. Therefore, we would like to do the experiment again with a new Trypsin. Also, it would be better to try with different proteases.

Future Works

From the results of our experiments, we confirmed that the proposed ideas were realized. To give ideas on a more broader span of ideas, we also thought of places this new nano-device could work in handy.

Finding New Aptamers for New and Different Substrates

We made DNA Shell like below (Fig.1), and additional DNA that specifically binds to a certain substance can be constructed on the Shell. By changing the arrangement of the DNA, you can capture whatever substance you like. As example, we experimented with biotin and streptavidin (Fig.2).


We thought of capturing thrombin. We could not experiment because of the shortage of time, but we made arrangements of the DNA that bind to thrombin, the thrombin aptamer. A part of the thrombin aptamer forms G-quartet structure to which thrombin binds(Fig. 3) (W Yoshida, K Sode, K Ikebukuro, Anal. Chem., 2006, 78 (10), pp 3297–3299).


Putting a part of thrombin aptamer on the center plane and other non-fixed plane of Shell (Fig. 4), Shell would close when thrombin comes near(Fig. 5).

Thrombin solidifies the blood, so the Shell that specifically binds to thrombin can prevent a blood clot. Like these, you can change the arrangement of the DNA on the Shell, and capture many kinds of substances. It makes DNA Shell a more useful device.

DNA Shell with Functionality

By putting DNA Shell and an enzyme together, you can use the Shell as a more functional device.

As example, we experimented with tetramethylbenzidine(TMB), horseradish peroxidase(HRP), and trypsin.

Like that experiment, by capturing the substrate, you can use the Shell as an inhibitor for enzyme (Fig.6).


Shell with a Logical Circuit

DNA Shell with the toehold medicated strand displacement reaction device

To get more advanced DNA Shell with a logical circuit, you can make the toehold medicated strand displacement reaction device on the Shell. In the strand displacement reaction, when a DNA is input, another DNA is released.


Design of the Logical Gates on DNA Shell

When attaching a biotin to the non-binding site of the DNA that is released in the strand displacement reaction, without the input DNA, streptavidin cannot combine with biotins because of the steric hindrance. However, once the DNA is input, the combination between streptavidin and biotins can be formed (Fig. 8).


The combination is formed only when two, three, or four biotin monomers are binding to streptavidin. Two strand displacement reaction devices can be constructed on both sides of the Shell (total four devices) (Fig. 9).


Each device catches the different input DNA. When the more than two biotins on the different Shell sides are gathering, the Shell will be closed (i.e., biotins on the A and B, or C and D gathering, the Shell will not be closed). So you can use four inputs.

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   <h2 style="border-bottom: none;">BIOMOD 2012 Team UT-Hongo</h2>
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<h3><a href="">Top</a></h3> <ul> <li><a href="">Abstract</a></li> <li><a href="">YouTube</a></li> <li><a href="">Links</a></li> </ul>

     <div class="footer-section" id="section2">

<h3><a href="">Motives</a></h3> <ul> <li><a href="">Focus</a></li> <li><a href="">Idea</a></li> <li><a href="">Funcitonalities</a></li>

         <li><a href="">Blueprint</a></li>


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<h3><a href="">Design & Results</a></h3> <ul> <li><a href="">Design</a></li>

         <li><a href="">Function</a></li>
         <li><a href="">Result</a></li>
         <li><a href="">Experiments</a></li>


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<h3><a href="">Method</a></h3> <ul> <li><a href="">AFM</a></li> <li><a href="">Photometer</a></li> <li><a href="">Electrophoresis</a></li> <li><a href="">Others</a></li> <li><a href="">Reagent</a></li> </ul>

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<h3><a href="">Progress & Beyond</a></h3> <ul> <li><a href="">Target Variety</a></li>

         <li><a href="">Functionalization</a></li>
         <li><a href="">Circuits</a></li>
         <li><a href="">Conclusion</a></li>


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<h3><a href="">Team</a></h3> <ul> <li><a href="">Info</a></li>

         <li><a href="">Members</a></li>
         <li><a href="">Mentors</a></li>
         <li><a href="">Photos</a></li>


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<h3><a href="">Acknowledgement</a></h3> <ul> <li><a href="">Mentor</a></li> <li><a href="">Professors</a></li> <li><a href="">Sponsors</a></li> <li><a href="">Special Thanks</a></li> </ul>

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     Copyright (C) 2012 | Design by Yuichi Nishwiaki | BIOMOD Team UT-Hongo
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