Biomod/2011/LMU/FolD'N'Assemble/Results: Difference between revisions
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The pictures of the TEM show that the cylinders have the right shape and size (Fig. 1). | The pictures of the TEM show that the cylinders have the right shape and size (Fig. 1). | ||
[[Image:Tem_monomere.jpg|thumb|500px|Fig.1: The monomers heve the designed size and shape]] | [[Image:Tem_monomere.jpg|thumb|center|500px|Fig.1: The monomers heve the designed size and shape]] | ||
===Dimerisation=== | ===Dimerisation=== | ||
Revision as of 13:18, 2 November 2011
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Summary of achievements
- The construct folded correctly.
- The cylinders dimerised correctly. The efficiency depends on the number of connections between the two cylinders
- The container openes at low pH depending on the salt concentration.
- The opening also would work in human cells because it works in PBS buffer.
- The container can be loaded by adding payload to the annealing buffer.
- Payload can be attached to the container by i-motif strands.
Folding
As a first step, we designed the construct and looked for the best folding conditions. We chose a cylindrical shape with a closed and an open end. CaDNAno-file: http://openwetware.org/wiki/Image:Nanopill.json
After some experiments, we decided to use a MgCl2 concentration of 18 mM and an annealing time of 55 h. The pictures of the TEM show that the cylinders have the right shape and size (Fig. 1).
Dimerisation
We designed four different constructs: with 2,3,4 and 5 pairs of complementary strands. The red strands include the i-motif and the blue strands are the complementary strands.
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More connection strands led to better dimerisation.
Opening
To open the containers we did a buffer exchange.
We exchanged the original buffer with another buffer with low pH. For good results we needed to decrease the salt concentration. With lower MgCl concentratione we got stronger monomer bands
To show that the opening process would work in the human cell, we used PBS buffer, which is isotonic to the human body.
