Biomod/2012/UTokyo/UT-Komaba/Experiment/Modified Origami: Difference between revisions
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[[Image:Biomod_2012_UTokyo_UT-Komaba_Experiment_ModifiedOrigamiConcept.png|center|Modified Origami Concept]] | [[Image:Biomod_2012_UTokyo_UT-Komaba_Experiment_ModifiedOrigamiConcept.png|center|Modified Origami Concept]] | ||
We | We combined DNA origami and pseudo-hammerhead structure so that, when cover DNAs hybridize to the structure, the hammerheads form and the surface of the modified origami shows a picture. | ||
Therefore, if we can set up the bistable system so that it produces the cover DNAs for different images, we can realize the DNA tablet. | Therefore, if we can set up the bistable system so that it produces the cover DNAs for different images, we can realize the DNA tablet. | ||
The purpose of the experiment is to make sure that the additional single strands necessary for the hammerhead structure DNAs do not disturb it during annealing in PCR. | The purpose of the experiment is to make sure that the additional single strands necessary for the hammerhead structure DNAs do not disturb it during annealing in PCR. | ||
We | We observed the modified DNA origami with cover DNAs by AFM. | ||
==Method== | ==Method== |
Revision as of 22:07, 27 October 2012
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Concept
We combined DNA origami and pseudo-hammerhead structure so that, when cover DNAs hybridize to the structure, the hammerheads form and the surface of the modified origami shows a picture. Therefore, if we can set up the bistable system so that it produces the cover DNAs for different images, we can realize the DNA tablet. The purpose of the experiment is to make sure that the additional single strands necessary for the hammerhead structure DNAs do not disturb it during annealing in PCR. We observed the modified DNA origami with cover DNAs by AFM.
Method
Pseudo-hammerhead Structure
To make hammerhead structure, we needed to add some DNA sequences to existing staples witch didn't interact with other parts of DNA origami. We made such sequences from the sequence below.
GGAACCTCAGCCCAACTAACAT |
This sequence is known not to interact with other parts of DNA origami. We made three hammerhead structures from this.
(5' -> 3' direction)
addition to staple | cover | |
---|---|---|
1 | CTCCAAGGTTT - TTTAGCCCAAC | GAGGTTCCTCGGGTTG |
2 | CGACTCCATTT - TTTCCAACTAA | TGGGCTGATGATTGTA |
3 | ACCCGACTTTT - TTTACTAACAT | GCTGAGGTGGTTGATT |
Experiment
October 3rd
We designed the modified origami and annealed them for about an hour in PCR. On the surface of one origami, there are 15 hammerhead structure and 1 hairpin structure. Therefore, we order DNA which composes the structures and replace staple strands of normal origami with them. We drew three lines on the surface by the hammerhead structures, and one line consisted of 5 hammerhead structures. The abstract design of the origami is the picture above.
October 5th
We made modified origami in October 3rd and keep them at the laboratory room temperture.
We observed the modified origami by AFM and we get the clear picture of lines on the surface of the origami.
The three lines on the surface shows the fact that the modified origami which have hammerhead structures was well-done.
Also, the picture below proved that we can observe a hammerhead structure as a dot so that we can draw a picture on the origami surface.
October 25th
The purpose of the experiment is to find out the reason why we could not observe the tablet by AFM in October 24th. To make sure whether we could not observe it because of AFM or not, we made modified origami which we succeeded in October 3rd. We made the modified origami in the same condition as that in October 3rd.