Biomod/2013/Aarhus/Materials And Methods/Origami

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Self-assembly of the plate

Plate assembly was optimized with respect to MgCl2 concentrations, time- and temperature ramps.

Self-assembly buffers (10X) contained 50mM Tris-HCl, 10mM EDTA, 50mM NaCl and MgCl2 in concentrations of 50 mM, 80 nM, 125 mM, 150 mM, 180 mM and 200 mM.

An example of a plate self-assembly reaction with 12.5 mM MgCl2 was prepared by mixing the following:

Table 3.

The module ’PepLock’ was replaceable with ’P-Lock’ of the same concentration for the experiments to connect plate and dome.

The samples were incubated in a GS4 PCR machine (G-storm) using a 17 hour non-linear annealing ramp.

17 hour non-linear ramp program

Rapid heating to 95 °C and incubation at 95 °C for 2 minutes

Cycle 1:-1.0 °C/cycle to 65 °C, cycle time = 30 seconds

Cycle 2:-1.0 °C/cycle to 15 °C, cycle time = 20 minutes

After ended program samples are stored at 4 °C

Self-assembly of the dome

Self-assembly buffers (10X) contained 50mM Tris-HCl, 10mM EDTA, 50mM NaCl and MgCl2 in concentrations of 50 mM, 80 nM, 125 mM, 150 mM, 180 mM and 200 mM.

An example of a dome self-assembly reaction with 12.5mM MgCl2 was prepared by mixing the following:

Table 4.

The module ’White’ was replaceable with the module ’D-zip’ of the same concentration for the experiments to connect plate and dome, and the module ’Purple’ could be replaced with ’Purple cy5’ of the same concentration.


After assembly, the samples were visualized on a 1% agarose gel containing 5mM MgCl2 and 0.5X TBE running buffer, also containing 5mM MgCl2. The gel was pre-stained with SYBR Safe (Invitrogen) and imaged on the Gel Dock (Bio-Rad) or on GE Healthcare Typhoon Trio gel scanning system. Loaded samples were prepared with Orange G with 10% glycerol and a 1kb Plus ladder from Invitrogen was used. Furthermore, AFM and TEM was used to characterize the origami structures.

Purification with freeze n’ squeeze

The sample was run on a 1 % agarose gel. The band of intereset was cut out and chopped into smaller pieces. The gel pieces were transferred to the filter and placed in a -20˚C freezer for 5 minutes. Subsequently, the filter was centrifuged at 13,000 × g for 15 minutes at room temperature. The agarose gel was retained inside the filter while the purified origamis were isolated in the column.

Purification with 100 kDA Amicon filters

The origami plate was purified using 100 kDA Amicon spin filters (Millipore). The filter was washed three times by adding 500 µL of the 1X self-assembly buffer to the filter and centrifuging at 4000 rpm for 8 minutes. The origami sample was added to the column along with the 1X self-assembly buffer to a tatol volume of 500 µL and centrifuged at 4000 rpm for 8 minutes. The column was three times more, before turning the filter upside-down in a fresh collection tube and eluting the sample by centrifuging at 4000 rpm for 2 minutes.

AFM characterization

The DNA origamis were imaged with AFM (Agilent Technologies®) in liquid tapping mode. The sample (1-2 μL) was mounted on a newly cleaved mica surface and left to adsorb for 1-2 minutes. Then 400 μL self-assembly buffer (1X) was added and the sample imaged with the software, PicoView (Agilent Technologies®).

Staining the samples for TEM

Approximately 10 µL of samples was pipetted onto a grids and left for 1 minute to dry. Remaining liquid was removed from the sample, and the sample was washed by adding H2O and subsequently removing excess liquid. Uranylacetate staining solution was added and the grid was left to stain for 1 minute before removing excess stain. The staining procedure was performed twice, and after 24 hours the samples were ready to be imaged using TEM .

Assembly of plate and dome

In preparation for the connection of the dome and plate a larger amount of both plate and dome was made, where the ’White’ module in the dome is replaced with ’D-zip’ and the ’PepLock’ module in the plate was replaced with ’P-Lock’ as follows:


Table 5.


Table 6.

1280 mL dome (1nM) was made in 32 separate 40 µL samples and 120 µL plate (21 nM) in 3 separate samples of 40 µL. The plate was purified with a 100 kDa Amicon spin filter. The dome was in separate experiments purified either with a 100 kDa Amicon spin filter or using freeze n’ squeeze. During purification of the plate a large excess of 1µM ‘WB-peplock’ (30µL) was added to the filter after the first wash and was left to anneal to the plate for 15 minutes, before unannealed excess of staple strands was washed off. The products of the purification of plate and dome were mixed in a 1:1 ratio and left to anneal at room temperature for 2.5 hours or in the GS4 PCR machine (G-Storm) at a linear annealing ramp, also for 2.5 hours.


Rapid heating to 60 °C and incubation at 60 °C for 6 minutes

Cycle 1:-1.0 °C/cycle, cycle time = 5 minutes

After ended program the samples are stored at 4 °C.

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</style> </head> <body> <div id="indexing"> <div id="sitemap"> <p id="sitemapTitle">SITEMAP | BIOMOD 2013 NANO CREATORS | Aarhus University</p> <div id="footer-contents"> <div class="footer-section"> <p class="footer-section-title">INTRODUCTION</p> <ul> <li><a href="/wiki/Biomod/2013/Aarhus">Home, abstract, animation and video</a></li> <li><a href="/wiki/Biomod/2013/Aarhus/Introduction">Introduction</a></li </ul> </div> <div class="footer-section"> <p class="footer-section-title">RESULTS AND DISCUSSION</p> <ul> <li><a href="/wiki/Biomod/2013/Aarhus/Results_And_Discussion/Origami">Origami</a></li> <li><a href="/wiki/Biomod/2013/Aarhus/Results_And_Discussion/Peptide_lock">Peptide lock</a></li> <li><a href="/wiki/Biomod/2013/Aarhus/Results_And_Discussion/Chemical_Modification">Chemical modification</a></li> <li><a href="/wiki/Biomod/2013/Aarhus/Results_And_Discussion/sisiRNA">sisiRNA</a></li> <li><a href="/wiki/Biomod/2013/Aarhus/Results_And_Discussion/System_In_Action">System in action</a></li> </ul> </div> <div class="footer-section"> <p class="footer-section-title">MATERIALS AND METHODS</p> <ul> <li><a href="/wiki/Biomod/2013/Aarhus/Materials_And_Methods/Origami">Origami</a></li> <li><a href="/wiki/Biomod/2013/Aarhus/Materials_And_Methods/Peptide_lock">Peptide lock</a></li> <li><a href="/wiki/Biomod/2013/Aarhus/Materials_And_Methods/Chemical_Modification">Chemical modification</a></li> <li><a href="/wiki/Biomod/2013/Aarhus/Materials_And_Methods/sisiRNA">sisiRNA</a></li> <li><a href="/wiki/Biomod/2013/Aarhus/Materials_And_Methods/System_In_Action">System in action</a></li> <li><a href="/wiki/Biomod/2013/Aarhus/Materials_And_Methods/Methods">Methods</a></li> </ul> </div> <div class="footer-section"> <p class="footer-section-title">SUPPLEMENTARY</p> <ul> <li><a href="/wiki/Biomod/2013/Aarhus/Supplementary/Team_And_Acknowledgments">Team and acknowledgments</a></li> <li><a href="/wiki/Biomod/2013/Aarhus/Supplementary/Optimizations">Optimizations</a></li> <li><a href="/wiki/Biomod/2013/Aarhus/Supplementary/Supplementary_Data">Supplementary data</a></li>


href="/wiki/Biomod/2013/Aarhus/Supplementary/Supplementary_Informations">Supplementary informations</a> <li><a href="/wiki/Biomod/2013/Aarhus/Supplementary/References">References</a></li> </ul> </div> </div> <div> <p id="copyright">Copyright (C) 2013 | BIOMOD Team Nano Creators @ Aarhus University | Programming by: <a href=" 2013:">Peter Vium Skaarup</a>.</p> </div> </div>

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