We are grateful for financial support from the NSFC (grants no. 91753134 and 21571100), and the State Key Laboratory of Bioelectronics of Southeast University.

1. Preparation of Circular DNAs
<ol>
	<li>Use all linear DNAs provided by commercial companies directly without further purification.</li>
	<li>Centrifuge the DNA samples at 5,000 &#215; g for 5 min to collect all DNA pellets at the bottom of the tubes. Add an appropriate volume of TE buffer (10 mM Tris, 1 mM EDTA, pH 8.0) to dissolve the DNA.</li>
	<li>Measure the concentration of &#34;a&#34; ng/&#181;L for each ss-DNA solution using a micro UV spectrometer at 260 nm. Convert &#34;a&#34; ng/&#181;L to &#34;b&#34; &#181;M following b = a &#215; 103 / (molecular weight of the DNA strand). Adjust the amount of TE solution to make a 10 &#181;M DNA stock solution.</li>
	<li>Use T4 DNA ligase to connect the 3&#39; and 5&#39; ends of 5&#39;-phosphorylated linear DNA templates ( Figure 1) of c64nt, c74nt and c84nt provided from commercial companies directly.</li>
	<li>Mix the 5&#39;-phosphorylated linear DNA strand (3.5 &#181;M) and its corresponding splint DNA strand (4.5 &#181;M) in 80 &#181;L TE buffer in a 200 &#181;L PCR test tube15. Incubate the tube in an open thermo bottle filled with 95 &#176;C water. Cool down the hot water to room temperature (25 &#176;C) for about 2-3 hours under the lab atmosphere.</li>
	<li>Add 10 &#181;L of 10x T4 buffer (660 mM Tris-HCl, 66 mM MgCl2, 100 mM DTT, 1 mM ATP) and 10 &#181;L of T4 ligase (300 U/&#181;L) to the mixture to a final volume of 100 &#181;L. Incubate the mixture in a thermocycler for 16 hours at 16 &#176;C. 
	NOTE: The above DNA concentrations and reaction volume of ~100 &#181;L are optimized for the high ligation efficiency and the high yield of correct oligo-monomer cyclization.&#160;Run two or more tubes of ligation reactions in the same time according to the experimental design. An alternative incubation procedure for ligation replacing step 1.6 is 4 hours at 25 &#176;C.</li>
	<li>After the incubation, inactivate the T4 ligase in 95 &#176;C water for 5 minminutes. Then transfer the tube to an ice water bath and incubate for 5 minutes to cool down.</li>
	<li>Add 10 &#181;L of 10x Exonuclease I buffer and 10 &#181;L of Exonuclease I (5 U/&#181;L) to the quenched mixture and incubate the tube at 37 &#176;C in a water bath for 30 min to selectively digest the remaining linear DNAs and leave the circularized DNAs intact.</li>
	<li>Prepare a 10% denaturing PAGE gel.
	<ol>
		<li>Wear rubber gloves and goggles when preparing the PAGE gel in the fume hood. Add 6.67 mL of 30% (w/v) acrylamide/bisacrylamide solution (19:1), 2 mL of 10x TAE&#183;Mg buffer (40 mM Tris, 40 mM HAc, 1 mM EDTA, pH 8.0 ,12.5 mM Mg(Ac)2), 8.4 g of urea (7 M) and deionized water to a final volume of 20 mL in a 40 mL centrifuge tube. 
		&#8203;Caution: The 30% (w/v) acrylamide/bisacrylamide solution (19:1) solution is toxic.</li>
		<li>Add 20 &#181;L of tetramethylethylenediamine (TEMED) and 100 &#181;L of ammonium persulfate (APS, 10% w/v) to the 40 mL tube before transfer the gel solution to the electrophoresis system immediately. Insert a 1.5 mm thick and 10-well comb. Wait at least 20 min until the gel solution is solidified.</li>
		<li>Set a constant voltage of 80 V for a gel of 85 &#215; 80 &#215; 1.5 mm3 (width &#215; height &#215; thickness). Add 1x TAE&#183;Mg buffer to the electrophoresis system and prerun the gel for 20 min at 10 V/cm.</li>
	</ol>
	</li>
	<li>Put the PCR test tube from step 1.8 in 95 &#176;C water for 5 min to inactivate Exonuclease I. Then transfer the tube to an ice water bath and incubate for another 5 min.</li>
	<li>Add 20 &#181;L of formamide in the tube to a final volume of 140 &#181;L and mix the solution. Distribute the solution to 7-9 denaturing PAGE gel wells equally with 16-20 &#181;L for each gel well. Mix 2 &#181;L of loading dye (0.05% bromophenol blue, 0.05% xylene cyanol FF, 60% glycerol, 10 mM Tris-HCl, 60 mM EDTA, pH 7.6) with 8 &#181;L of the corresponding precursor linear DNA (10 &#181;M) and inject the mixture to a separate well for reference. 
	NOTE: The addition of formamide is to increase the density of the loading solution for sinking to the bottom of the PAGE gel well and also to disassociate some double stranded DNA residues.</li>
	<li>Run the gel for about 2 h at 10 V/cm and stop running when xylene cyanol FF is at the 2/3 position of the glass plate with the naked eye.</li>
	<li>Wear rubber gloves and goggles to protect skins and eyes. Take the gel out of the glass plate. Place the gel on a fluorescent TLC (thin layer chromatography) plate. Cut off the target gel bands by a razor blade as exactly as shadowed by UV irradiation (Figure 2). 
	Caution: The UV light is harmful to eyes and skins. 
	NOTE: Under UV irradiation at 254 nm, DNA will absorb the light and cast a shadow onto the TLC plate. The circular DNA ran slightly slower than its corresponding precursor linear DNA. Some undigested linear DNAs and unwanted circular DNAs in small amounts which surround the shadowed target band will pollute the circular DNA if they are collected.</li>
	<li>Transfer the gel bands into a 2.0 mL microcentrifuge tube. Air dry or blow dry the gel bands and then mash the gels into a paste by a spatula or flattened glass rod. Make sure the gel has been completely crushed into a paste, which is critical to the high yield of circular DNA. Add twice of the gel volume deionized water into the tube and shake the tube at room temperature overnight.</li>
	<li>Filter the mixture to collect the supernatants in a 2.0 mL microcentrifuge tube. Recover any residual DNA by rinsing with small volume of deionized water and filter again to combine the supernatants.&#160;</li>
	<li>Extract the eluent with equal volume of n-butanol. Repeat this procedure until the aqueous volume is reduced to about 200 &#181;L.</li>
	<li>Add 500 &#181;L of absolute ethanol (&#8722;20 &#176;C) and 20 &#181;L of 3 M NaOAc (pH 5.1) to the mixture for DNA precipitation. Store the tube at &#8722;20 &#176;C for 30 min.</li>
	<li>Centrifuge the tube at 12,000 &#215; g for 10 min at 4 &#176;C, discard the supernatant. The remaining DNA precipitate is about 100 &#181;L in the tube.</li>
	<li>Add 600 &#181;L of 75% ethanol (&#8722;20 &#176;C) to the tube and store it at &#8722;20 &#176;C for 30 min. Then centrifuge at 12,000 &#215; g for 10 min at 4 &#176;C, discard the supernatant. The remaining DNA precipitate is about 100 &#181;L solution in the tube again. Repeat the procedure twice.</li>
	<li>After the last centrifugation, discard the supernatant as much as possible. Dry the remains with a vacuum concentrator.</li>
	<li>Store the purified circular DNA in the tube at &#8722;20 &#176;C.</li>
	<li>Resuspend the circular DNA in TE buffer to make a 10 &#181;M circular DNA stock solution according to step 1.3 when needed.</li>
</ol>
2. Annealing of Assembly Solutions
<ol>
	<li>Prepare each tile or nanostructural assembly solution of c64bp, c84bp, HJ-c64nt, aHJ-c64nt, HJ-c84nt, tHJ-c84nt, cDAO-c64nt, acDAO-c64nt, cDAO-c84nt, c64nt, c84nt, and acDAO-c64nt-E with a designed set of linear and circular DNAs for one-pot annealing.
	<ol>
		<li>For each assembly solution, mix 2 &#181;L of 10x TAE&#183;Mg buffer, 1 &#181;L of each DNA stock solution of a set of linear and circular strands in equal molar ratios, and additional TE buffer in a 200 &#181;L PCR test tube to a final concentration of each strand at 0.5 &#181;M and a final volume of 20 &#181;L. Anneal the assembly solution in a thermo bottle from 95 &#176;C to 25 &#176;C over 48 h.</li>
	</ol>
	</li>
	<li>Prepare each assembly solution of 2D infinite lattices of cDAO-c64nt-E, cDAO-c64nt-O, cDAO-c84nt-E, and cDAO-c84nt-O with a designed set of linear and circular DNAs for two-step annealing.
	<ol>
		<li>Prepare each precursor sub-tile assembly solution by mixing 2 &#181;L of 10x TAE&#183;Mg buffer, 1 &#181;L of each DNA stock solution of a set of linear and circular strands in equal molar ratios, and additional TE buffer in a 200 &#181;L PCR test tube to a final concentration of 0.5 &#181;M for each strand and a final volume of 20 &#181;L. In the first sub-tile annealing step, anneal each precursor sub-tile solution in a PCR thermocycler using a fast-linear cooling method from 95 &#176;C to 25 &#176;C over 2.5 h.</li>
		<li>Prepare each assembly solution of the above four infinite lattices by mixing&#160;10 &#181;L of each of the two corresponding sub-tile solutions together to a final concentration of 0.25 &#181;M for each strand. In the second lattice annealing step, anneal the 20 &#181;L mixture in a PCR thermocycler using a slow cooling method of staying at 50 &#176;C for 2 h and cooling down at a rate of 0.1 &#176;C per 5 minutes to 20 &#176;C, about 24 h in total. 
		NOTE: Two parallel experiments can be run simultaneously or subsequently in the second annealing step for each 2D infinite lattice.</li>
	</ol>
	</li>
	<li>Prepare assembly solutions of two finite rectangle assemblies of 5 &#215; 6 cDAO-c64nt-O and 5 &#215; 6 cDAO-c74&#38;c84nt-O for two-step annealing.
	<ol>
		<li>Prepare each precursor sub-tile assembly solution by mixing 1 &#181;L of 10x TAE&#183;Mg buffer, 0.5 &#181;L of each DNA stock solution of a set of linear and circular strands in equal molar ratios, and additional TE buffer in a 200 &#181;L PCR test tube to a final concentration of 0.5 &#181;M for each strand and a final volume of 10 &#181;L. In the first annealing step, anneal each precursor sub-tile solution in a PCR thermocycler using a fast-linear cooling method from 95 &#176;C to 25 &#176;C over 2.5 h.</li>
		<li>Prepare each finite rectangle lattice assembly solution by mixing 32 x (2 &#181;L of each sub-tile solution) together in a 200 &#181;L PCR test tube to a final concentration of ~15 nM for each sub-tile and a final volume of 64 &#181;L. In the second annealing step, anneal the 64 &#181;L mixture in a PCR thermocycler using a slow cooling method of staying at 50 &#176;C for 2 h and cooling down at a rate of 0.1 &#176;C per 5 min to 20 &#176;C, about 24 hours in total. 
		NOTE: Five parallel experiments can be run simultaneously or subsequently in the second annealing step for each finite rectangle assembly.</li>
	</ol>
	</li>
</ol>
3. Native PAGE Analysis
<ol>
	<li>Prepare a 10% native PAGE following step 1.9 except for the urea component.</li>
	<li>For control samples of c64bp and c84bp, add 2 &#181;L of each assembly solution and 1 &#181;L of loading dye to 3 &#181;L of TE buffer as controls separately. For each of other assemblies listed in Figure 3, add 1 &#181;L of each assembly solution and 1 &#181;L of loading dye to 4 &#181;L of TE buffer.</li>
	<li>Inject each of the above solutions to a gel well. Add 5 &#181;L of DNA marker (25-500 bp) to a separate well for reference.</li>
	<li>Run the gel for about 4 hours at 10 V/cm in an ice water bath. The xylene cyanol FF will run out of the glass plate.</li>
	<li>Wear rubber gloves and goggles to protect skins and eyes. Take the gel out of the glass plate and immerse it in 100 mL of deionized water with 10 &#181;L of a nucleic acid gel stain for 30 min. 
	Caution: The nucleic acid gel stain solution is toxic.</li>
	<li>Observe the gel under an UV imaging system and take a picture of the stained gel (Figure 3).</li>
</ol>
4. Purification of Finite Lattices
<ol>
	<li>Prepare a native 2% agarose gel for electrophoresis purification of finite lattices.
	<ol>
		<li>Mix 1 g of agarose powder, 5 mL of 10x TBE&#183;Mg buffer (89 mM Tris, 89 mM Boric Acid, 2 mM EDTA, pH 8.0, 12.5 mM Mg(Ac)2), 2 &#181;L of nucleic acid gel stain and 47.5 mL of deionized water in a 250 mL triangle bottle. Boil the mixture until the bubbles become small and dense. Add hot water in the bottle to a total volume of 50 mL and a concentration of 2% agarose.</li>
		<li>Wear thick gloves. Pour the gel solution into a plastic gel box of 7 x 10 x 1 cm3 (width &#215; length &#215; thickness). Insert a 1.5 mm thick and 12-well gel comb. Wait for the gel to cool down to room temperature. If necessary, put the gel in a 4 &#176;C fridge. 
		Caution: Be aware of scalding because the solution is very hot.</li>
		<li>Add 0.5x TBE&#183;Mg buffer in the electrophoresis system. Prerun the gel at 5 V/cm for 20 min in an ice water bath at a constant voltage of 50 V.</li>
		<li>Inject 20 &#181;L of the finite lattice solution prepared in step 2.3 in each agarose gel well and add 5 &#181;L of a DNA marker (100-3,000 bp) to a separate well. Run the gel for 2 h at 5 V/cm in an ice water bath.</li>
		<li>Wear rubber gloves and goggles to protect skins and eyes. Cut the target gel bands with a position similar to the 1,000 bp marker under UV light and slice them into fine pieces and place the crushed gels into a filter column8.</li>
		<li>Centrifuge the column at 2,000 x g for 5 min at 4 &#176;C. Extract the sample solution through the column. Collect the solution for AFM imaging.</li>
	</ol>
	</li>
	<li>Purify finite lattices by PEG precipitation.
	<ol>
		<li>Mix 50 &#181;L of the finite lattice solution prepared in step 2.3 with an equal volume of 15% PEG8000 (w/v) buffer (20 mM Mg(Ac)2, 5 mM Tris, 1 mM EDTA and 505 mM NaCl)22. Centrifuge the solution at 18,000 &#215; g at 4 &#176;C for 30 min.</li>
		<li>Remove the supernatant and add 100 &#181;L of PEG buffer. Repeat the centrifugation.</li>
		<li>After removing the supernatant, dissolve the pellet in 1x TAE&#183;Mg buffer for AFM imaging. 
		NOTE: Purification is necessary for the finite lattices of 5 &#215; 6 cDAO-c64nt-O and 5 &#215; 6 cDAO-c74&#38;c84nt-O for AFM imaging and other applications. If the yield is too low, increase the centrifugation speed. If the product is not pure enough, repeat step 4.2.2.</li>
	</ol>
	</li>
</ol>
5. AFM Imaging
<ol>
	<li>For c64nt nanowire, c84nt nanowire, acDAO-c64nt-E, infinite 2D lattices of cDAO-c64nt-E(O), and cDAO-c84nt-E(O), deposit 2 &#956;L of annealed sample on a freshly cleaved mica surface. Leave for 2 min for adsorption of DNA lattices to the mica surface. Wash the surface with 100 &#181;L of deionized water twice and dry it by compressed air.</li>
	<li>Obtain AFM images of infinite DNA lattices in air by scanning the mica surface with triangular AFM probes under tapping mode. Set the following parameters for scanning: scan size of 0.5~5 &#181;m, scan resolution of 512 lines, and scan rate of 3.5 Hz (Figure 4).</li>
	<li>For finite DNA lattices of 5 &#215; 6 cDAO-c64nt-O and 5 &#215; 6 cDAO-c74&#38;c84nt-O,&#160;deposit 80 &#181;L of 1x TAE&#183;Mg buffer on a freshly cleaved mica surface. Then add 5 &#181;L of finite samples into the buffer. Leave for 2 min for adsorption of DNA lattices to the mica surface. Add another 50 &#181;L of 1x TAE&#183;Mg buffer on the AFM probe.</li>
	<li>Obtain AFM images of finite DNA lattices in fluid by scanning the mica surface with triangular AFM probes under tapping mode. Set the following parameters for scanning: scan size of 0.5-1 &#181;m, scan resolution of 256 lines, and scan rate of 1.5 Hz (Figure 5).</li>
</ol>

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The authors have no conflicts of interest to disclose.

The protocols presented in this article focus on the synthesis of small circular DNA molecules and the assembly of DNA nanostructures. Most of randomly-sequenced DNA designs can be used in this protocol. The purity of circular DNAs is critical for the success of DNA assemblies. The production yield of cyclization can be improved by lowering the concentration of 5'-phosphorylated linear DNA; however, this will increase the workload to produce the same amounts of circular DNAs. The length of splint DNA strands also affects...

DNA molecules have been used to build many kinds of nanostructures over decades. Typical motifs include DAE (double crossover, antiparallel, even half-turns) and DAO tiles1,2,3, star tiles4,5,6,7, single stranded (ss) tiles8,9,10, and DNA origami11,12,13. These DNA motifs and lattices are assembled from linear ss-DNAs. Recently, others and we have reported the use of circular ss-oligonucleotides as scaffolds to build motifs, 1D nanotubes, and 2D lattices14,15,16,17. By inserting a Holliday junction (HJ)18,19,20,21 at the center of c64nt, a pair of two coupled DAO tiles can be formed17. This new cDAO motif and its derivatives are stable and rigid enough to assemble 2D DNA lattices up to 3 &#215; 5 &#181;m2. In this paper, we use a term of &#34;circular tile&#34;, which is defined as a stable DNA complex molecule constructed with one circular scaffold and other linear staples of ss-oligonucleotides, and another term of &#34;linear tile&#34;, which is built from a full set of linear ss-oligonucleotides.
This protocol demonstrates how to construct five kinds of DNA nanostructures with small circular DNA molecules as scaffolds: 1) infinite 1D c64nt and c84nt nanowires, 2) infinite 2D cDAO-c64nt-O and cDAO-c64nt-E (-O represents an odd number&#160;of 5 half-turns and -E represents an even number&#160;of 4 half-turns) lattices, 3) infinite 2D cDAO-c84nt-O and cDAO-c84nt-E lattices, 4) finite 2D 5 &#215; 6 cDAO-c64nt-O and 5 &#215; 6 cDAO-c74&#38;84nt-O rectangles, 5) infinite 1D acDAO-c64nt-E nanorings and nanospirals (please refer to Figure&#160;3-5 for the schematic drawings and images of the above five kinds of DNA nanostructures). The 1D c64nt and c84nt nanowires are assembled from each c64nt and c84nt scaffold associated with two linear staples respectively. Each circular tile of cDAO-c64nt, acDAO-c64nt, cDAO-c74nt, or&#160;cDAO-c84nt is annealed from its corresponding scaffold of c64nt, c74nt, or c84nt with four linear staples respectively. The infinite 2D lattices are assembled from the same type of two circular tiles with different sequences. The two finite 2D rectangle lattices are assembled from two&#160;sets of 32 circular sub-tiles respectively. To save money, only one-sequenced c64nt, c74nt, and c84nt is used as the respective scaffold while different overhangs are used to anneal the 32 cDAO-c64nt, 12 cDAO-c74nt, and 20 cDAO-c84nt circular sub-tiles respectively in the first sub-tile annealing step, then mix the corresponding 32 circular sub-tiles together and apply the second lattice annealing step to assemble the finite 5 &#215; 6 cDAO-c64nt-O and 5 &#215; 6 cDAO-c74&#38;84nt-O lattices, respectively. Definitely, differently-sequenced circular scaffolds can be adopted to assemble a variety of finite size nanostructures, however it will cost more money and labors. The infinite 1D acDAO-c64nt-E nanorings and nanospirals are annealed from one-sequenced asymmetric acDAO-c64nt tiles with linear connections of an even number of 4 half-turns. There are two approaches to assemble infinite 2D lattices from circular tiles of cDAO-c64nt and cDAO-c84nt, which are distinguished by the intertile distances of an even number of 4 and an odd number of 5 half-turns respectively. The former requires all tiles to be aligned identically; the latter requires alternation of the faces of two neighboring tiles along the helical axes. If the tile is rigid and planar, such as cDAO-c64nt, both approaches will generate planar nanoribbons; if the tile is curved towards one direction, such as cDAO-c84nt, the intertile connection of an even number of 4 half turns will generate nanotubes, whereas the intertile connection of an odd number of 5 half turns will produce planar nanoribbons due to elimination of curvature-biased growth by alternate&#160;alignment of curved tiles. The successful assembly of 1D and 2D DNA nanostructures from circular tiles indicates several advantages of this new approach: enforced stability and rigidity of circular tiles over linear tiles, chiral tiles for assembly of asymmetrical nanostructures such as nanorings and nanoribbons, new visions on understanding the DNA mechanics and molecular structures, etc.

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			<td height="21" style="height:21px;width:216px;">T4 ligase</td>
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			<td height="21" style="height:21px;width:216px;">Exonuclease I buffer</td>
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			<td height="42" style="height:42px;width:216px;">30% (w/v) Acryl/Bis solution (19:1)</td>
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			<td height="21" style="height:21px;width:216px;">TAE premix podwer</td>
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			<td height="42" style="height:42px;width:216px;">Mg(Ac)2&#183;4H2O</td>
			<td style="width:171px;">Nanjing Chemical Reagent</td>
			<td style="width:131px;">C0190550223</td>
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			<td height="21" style="height:21px;width:216px;">Urea</td>
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			<td style="width:131px;">A510907</td>
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		<tr height="21">
			<td height="21" style="height:21px;width:216px;">TEMED</td>
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			<td style="width:131px;">A100761</td>
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		<tr height="42">
			<td height="42" style="height:42px;width:216px;">Ammonium Persulfate</td>
			<td style="width:171px;">Nanjing Chemical Reagent</td>
			<td style="width:131px;">13041920295</td>
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		<tr height="21">
			<td height="21" style="height:21px;width:216px;">Power supply</td>
			<td style="width:171px;">Beijing Liuyi</td>
			<td style="width:131px;">DYY-8C</td>
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			<td height="21" style="height:21px;width:216px;">Water bath</td>
			<td style="width:171px;">Sumsung</td>
			<td style="width:131px;">DK-S12</td>
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			<td height="21" style="height:21px;width:216px;">Formamide</td>
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			<td height="21" style="height:21px;width:216px;">DNA Marker (25~500 bp)</td>
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			<td height="21" style="height:21px;width:216px;">DNA Marker (100~3000 bp)</td>
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			<td height="21" style="height:21px;width:216px;">Loading buffer</td>
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			<td height="21" style="height:21px;width:216px;">PAGE electrophoresis systerm</td>
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			<td style="width:131px;">5010-2225</td>
			<td>0.22 &#181;M</td>
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			<td height="21" style="height:21px;width:216px;">UV imaging System</td>
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			<td style="width:131px;">2500R</td>
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			<td height="21" style="height:21px;width:216px;">n-butanol</td>
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			<td height="21" style="height:21px;width:216px;">Absolute Ethanol</td>
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			<td height="42" style="height:42px;width:216px;">NaOAc</td>
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			<td height="42" style="height:42px;width:216px;">Agarose electrophoresis systerm</td>
			<td style="width:171px;">Beijing Liuyi</td>
			<td style="width:131px;">DYCP-31CN</td>
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			<td height="21" style="height:21px;width:216px;">Heating Plate</td>
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			<td style="width:131px;">DB-1</td>
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		<tr height="21">
			<td height="21" style="height:21px;width:216px;">TBE premix podwer&#160;</td>
			<td style="width:171px;">Sangon</td>
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		<tr height="21">
			<td height="21" style="height:21px;width:216px;">filter column</td>
			<td style="width:171px;">Bio-Rad</td>
			<td style="width:131px;">7326165</td>
			<td>Freeze &#39;N Squeeze column</td>
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		<tr height="42">
			<td height="42" style="height:42px;width:216px;">AFM</td>
			<td style="width:171px;">Bruker</td>
			<td style="width:131px;">Dimension FastScan</td>
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		<tr height="21">
			<td height="21" style="height:21px;width:216px;">PEG8000</td>
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			<td style="width:131px;">A100159</td>
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			<td height="21" style="height:21px;width:216px;">Mica</td>
			<td style="width:171px;">Ted Pella</td>
			<td style="width:131px;">BP50</td>
			<td></td>
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		<tr height="21">
			<td height="21" style="height:21px;width:216px;">triangular AFM probe in air</td>
			<td style="width:171px;">Bruker</td>
			<td style="width:131px;">FastScan-C</td>
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		<tr height="21">
			<td height="21" style="height:21px;width:216px;">triangular AFM probe in fulid</td>
			<td style="width:171px;">Bruker</td>
			<td style="width:131px;">ScanAsyst-fluid+</td>
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		<tr height="21">
			<td height="21" style="height:21px;width:216px;">DNA strands</td>
			<td style="width:171px;">Sangon</td>
			<td style="width:131px;"></td>
			<td></td>
		</tr>
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stable dna motifs, 1d and 2d nanostructures constructed from small circular dna molecules

This article presents a detailed protocol for synthesis of small circular DNA molecules, annealing of circular DNA motifs, and construction of 1D and 2D DNA nanostructures. Over decades, the rapid development of DNA nanotechnology is attributed to the use of linear DNAs as the source materials. For example, the DAO (double crossover, antiparallel, odd half-turns) tile is well-known as a building block for construction of 2D DNA lattices; the core structure of DAO is made from two linear single-stranded (ss) oligonucleotides, like two ropes making a right hand granny&#160;knot. Herein, a new type of DNA tiles called cDAO (coupled DAO) are built using a small circular ss-DNA of c64nt or c84nt (circular 64 or 84 nucleotides) as the scaffold strand and several linear ss-DNAs as the staple strands. Perfect 1D and 2D nanostructures are assembled from cDAO tiles: infinite nanowires, nanospirals, nanotubes, nanoribbons; and finite nano-rectangles. Detailed protocols are described: 1) preparation by T4 ligase and purification by denaturing PAGE (polyacrylamide gel electrophoresis) of small circular oligonucleotides, 2) annealing of stable circular tiles, followed by native PAGE analysis, 3) assembling of infinite 1D nanowires, nanorings, nanospirals, infinite 2D lattices of nanotubes and nanoribbons, and finite 2D nano-rectangles, followed by AFM (Atomic Force Microscopy) imaging. The method is simple, robust, and affordable for most labs.

The circular DNA moves slightly slower than its precursor linear DNA in denaturing PAGE (Figure 2) because the pore inside the circular DNA is penetrated and retarded by gel fibers23,24,25. The correct ligation reaction efficiency for oligo-monomer cyclization depends on the substrate sequence and concentration, reaction temperature, time, etc. As the concen...

Watch this Scientific Journal Video about Stable DNA Motifs, 1D and 2D Nanostructures Constructed from Small Circular DNA Molecules at JoVE.com

Stable DNA Motifs, 1D and 2D Nanostructures Constructed from Small Circular DNA Molecules

This article presents a detailed protocol for T4 ligation and denaturing PAGE purification of small circular DNA molecules, annealing and native PAGE analysis of circular tiles, assembling and AFM imaging of 1D and 2D DNA nanostructures, as well as agarose gel electrophoresis and centrifugation purification of finite DNA nanostructures.

This article presents a detailed protocol for synthesis of small circular DNA molecules, annealing of circular DNA motifs, and construction of 1D and 2D ...

stable-dna-motifs-1d-2d-nanostructures-constructed-from-small

Universidad de Cartagena UDEC

Research

JoVE Journal

Chemistry

6.3K Views.  Nanjing University. This article presents a detailed protocol for T4 ligation and denaturing PAGE purification of small circular DNA molecules, annealing and native PAGE analysis of circular tiles, assembling and AFM imaging of 1D and 2D DNA nanostructures, as well as agarose gel electrophoresis and centrifugation purification of finite DNA nanostructures. 

Video: Stable DNA Motifs, 1D and 2D Nanostructures Constructed from Small Circular DNA Molecules

Rapid Colorimetric Assays to Qualitatively Distinguish RNA and DNA in Biomolecular Samples

Biochemical experimentation generally requires accurate knowledge, at an early stage, of the nucleic acid, protein, and other biomolecular components in potentially heterogeneous specimens. Nucleic acids can be detected via several established approaches, including analytical methods that are spectrophotometric (e.g., A260), fluorometric (e.g., binding of fluorescent dyes), or colorimetric (nucleoside-specific chromogenic chemical reactions).1 Though it cannot readily distinguish RNA from DNA, the A260/A280 ratio is commonly employed, as it offers a simple and rapid2 assessment of the relative content of nucleic acid, which absorbs predominantly near 260 nm and protein, which absorbs primarily near 280 nm. Ratios &lt; 0.8 are taken as indicative of 'pure' protein specimens, while pure nucleic acid (NA) is characterized by ratios &gt; 1.53.
However, there are scenarios in which the protein/NA content cannot be as clearly or reliably inferred from simple uv-vis spectrophotometric measurements. For instance, (i) samples may contain one or more proteins which are relatively devoid of the aromatic amino acids responsible for absorption at &asymp;280 nm (Trp, Tyr, Phe), as is the case with some small RNA-binding proteins, and (ii) samples can exhibit intermediate A260/A280 ratios (~0.8 &lt; ~1.5), where the protein/NA content is far less clear and may even reflect some high-affinity association between the protein and NA components. For such scenarios, we describe herein a suite of colorimetric assays to rapidly distinguish RNA, DNA, and reducing sugars in a potentially mixed sample of biomolecules. The methods rely on the differential sensitivity of pentoses and other carbohydrates to Benedict's, Bial's (orcinol), and Dische's (diphenylamine) reagents; the streamlined protocols can be completed in a matter of minutes, without any additional steps of having to isolate the components. The assays can be performed in parallel to differentiate between RNA and DNA, as well as indicate the presence of free reducing sugars such as glucose, fructose, and ribose (Figure 1).

A suite of colorimetric assays is described for rapidly distinguishing protein, RNA, DNA, and reducing sugars in potentially heterogeneous biomolecular samples.

Biochemical experimentation generally requires accurate knowledge, at an early stage, of the nucleic acid, protein, and other biomolecular components in ...

Gyroid Nickel Nanostructures from Diblock Copolymer Supramolecules

Nanoporous metal foams possess a unique combination of properties - they are catalytically active, thermally and electrically conductive, and furthermore, have high porosity, high surface-to-volume and strength-to-weight ratio. Unfortunately, common approaches for preparation of metallic nanostructures render materials with highly disordered architecture, which might have an adverse effect on their mechanical properties. Block copolymers have the ability to self-assemble into ordered nanostructures and can be applied as templates for the preparation of well-ordered metal nanofoams. Here we describe the application of a block copolymer-based supramolecular complex - polystyrene-block-poly(4-vinylpyridine)(pentadecylphenol) PS-b-P4VP(PDP) - as a precursor for well-ordered nickel nanofoam. The supramolecular complexes exhibit a phase behavior similar to conventional block copolymers and can self-assemble into the bicontinuous gyroid morphology with two PS networks placed in a P4VP(PDP) matrix. PDP can be dissolved in ethanol leading to the formation of a porous structure that can be backfilled with metal. Using electroless plating technique, nickel can be inserted into the template&#39;s channels. Finally, the remaining polymer can be removed via pyrolysis from the polymer/inorganic nanohybrid resulting in nanoporous nickel foam with inverse gyroid morphology.

This article describes the preparation of well-ordered nickel nanofoams via electroless metal deposition onto nanoporous templates obtained from self-assembled diblock copolymer based supramolecules.

Nanoporous metal foams possess a unique combination of properties - they are catalytically active, thermally and electrically conductive, and furthermore, ...

Structure and Coordination Determination of Peptide-metal Complexes Using 1D and 2D 1H NMR

Copper (I) binding by metallochaperone transport proteins prevents copper oxidation and release of the toxic ions that may participate in harmful redox reactions. The Cu (I) complex of the peptide model of a Cu (I) binding metallochaperone protein, which includes the sequence MTCSGCSRPG (underlined is conserved), was determined in solution under inert conditions by NMR spectroscopy.
NMR is a widely accepted technique for the determination of solution structures of proteins and peptides. Due to difficulty in crystallization to provide single crystals suitable for X-ray crystallography, the NMR technique is extremely valuable, especially as it provides information on the solution state rather than the solid state. Herein we describe all steps that are required for full three-dimensional structure determinations by NMR. The protocol includes sample preparation in an NMR tube, 1D and 2D data collection and processing, peak assignment and integration, molecular mechanics calculations, and structure analysis. Importantly, the analysis was first conducted without any preset metal-ligand bonds, to assure a reliable structure determination in an unbiased manner.

Structure and Coordination Determination of Peptide-metal Complexes Using 1D and 2D 1H NMR

The NMR-solution structure of a metallochaperone model peptide with Cu (I) was determined, and a detailed protocol from sample preparation and 1D and 2D data collection to a three-dimensional structure is described.

Copper (I) binding by metallochaperone transport proteins prevents copper oxidation and release of the toxic ions that may participate in harmful redox ...

Folding and Characterization of a Bio-responsive Robot from DNA Origami

The DNA nanorobot is a hollow hexagonal nanometric device, designed to open in response to specific stimuli and present cargo sequestered inside. Both stimuli and cargo can be tailored according to specific needs. Here we describe the DNA nanorobot fabrication protocol, with the use of the DNA origami technique. The procedure initiates by mixing short single-strand DNA staples into a stock mixture which is then added to a long, circular, single-strand DNA scaffold in presence of a folding buffer. A standard thermo cycler is programmed to gradually lower the mixing reaction temperature to facilitate the staples-to-scaffold annealing, which is the guiding force behind the folding of the nanorobot. Once the 60 hr folding reaction is complete, excess staples are discarded using a centrifugal filter, followed by visualization via agarose-gel electrophoresis (AGE). Finally, successful fabrication of the nanorobot is verified by transmission electron microscopy (TEM), with the use of uranyl-formate as negative stain.

DNA origami is a powerful method for fabricating precise nanoscale objects by programming the self-assembly of DNA molecules. Here we describe a protocol for the folding of a bio-responsive robot from DNA origami, its purification and negative staining for transmission electron microscopic imaging (TEM).

The DNA nanorobot is a hollow hexagonal nanometric device, designed to open in response to specific stimuli and present cargo sequestered inside. Both ...

Self-assembly of Complex Two-dimensional Shapes from Single-stranded DNA Tiles

Current methods in DNA nano-architecture have successfully engineered a variety of 2D and 3D structures using principles of self-assembly. In this article, we describe detailed protocols on how to fabricate sophisticated 2D shapes through the self-assembly of uniquely addressable single-stranded DNA tiles which act as molecular pixels on a molecular canvas. Each single-stranded tile (SST) is a 42-nucleotide DNA strand composed of four concatenated modular domains which bind to four neighbors during self-assembly. The molecular canvas is a rectangle structure self-assembled from SSTs. A prescribed complex 2D shape is formed by selecting the constituent molecular pixels (SSTs) from a 310-pixel molecular canvas and then subjecting the corresponding strands to one-pot annealing. Due to the modular nature of the SST approach we demonstrate the scalability, versatility and robustness of this method. Compared with alternative methods, the SST method enables a wider selection of information polymers and sequences through the use of de novo designed and synthesized short DNA strands.

DNA tiling is an effective approach to make programmable nanostructures. We describe the protocols to construct complex two-dimensional shapes by the self-assembly of single-stranded DNA tiles.

Current methods in DNA nano-architecture have successfully engineered a variety of 2D and 3D structures using principles of self-assembly. In this ...

Preparation of Mica and Silicon Substrates for DNA Origami Analysis and Experimentation

The designed nature and controlled, one-pot synthesis of DNA origami provides exciting opportunities in many fields, particularly nanoelectronics. Many of these applications require interaction with and adhesion of DNA nanostructures to a substrate. Due to its atomically flat and easily cleaned nature, mica has been the substrate of choice for DNA origami experiments. However, the practical applications of mica are relatively limited compared to those of semiconductor substrates. For this reason, a straightforward, stable, and repeatable process for DNA origami adhesion on derivatized silicon oxide is presented here. To promote the adhesion of DNA nanostructures to silicon oxide surface, a self-assembled monolayer of 3-aminopropyltriethoxysilane (APTES) is deposited from an aqueous solution that is compatible with many photoresists. The substrate must be cleaned of all organic and metal contaminants using Radio Corporation of America (RCA) cleaning processes and the native oxide layer must be etched to ensure a flat, functionalizable surface. Cleanrooms are equipped with facilities for silicon cleaning, however many components of DNA origami buffers and solutions are often not allowed in them due to contamination concerns. This manuscript describes the set-up and protocol for in-lab, small-scale silicon cleaning for researchers who do not have access to a cleanroom or would like to incorporate processes that could cause contamination of a cleanroom CMOS clean bench. Additionally, variables for regulating coverage are discussed and how to recognize and avoid common sample preparation problems is described.

Reproducible cleaning processes for substrates used in DNA origami research are described, including bench-top RCA cleaning and derivatization of silicon oxide. Protocols for surface preparation, DNA origami deposition, drying parameters, and simple experimental set-ups are illustrated.

The designed nature and controlled, one-pot synthesis of DNA origami provides exciting opportunities in many fields, particularly nanoelectronics. Many of ...

Highly Stable, Functional Hairy Nanoparticles and Biopolymers from Wood Fibers: Towards Sustainable Nanotechnology

Nanoparticles, as one of the key materials in nanotechnology and nanomedicine, have gained significant importance during the past decade. While metal-based nanoparticles are associated with synthetic and environmental hassles, cellulose introduces a green, sustainable alternative for nanoparticle synthesis. Here, we present the chemical synthesis and separation procedures to produce new classes of hairy nanoparticles (bearing both amorphous and crystalline regions) and biopolymers based on wood fibers. Through periodate oxidation of soft wood pulp, the glucose ring of cellulose is opened at the C2-C3 bond to form 2,3-dialdehyde groups. Further heating of the partially oxidized fibers (e.g., T = 80 &#176;C) results in three products, namely fibrous oxidized cellulose, sterically stabilized nanocrystalline cellulose (SNCC), and dissolved dialdehyde modified cellulose (DAMC), which are well separated by intermittent centrifugation and co-solvent addition. The partially oxidized fibers (without heating) were used as a highly reactive intermediate to react with chlorite for converting almost all aldehyde to carboxyl groups. Co-solvent precipitation and centrifugation resulted in electrosterically stabilized nanocrystalline cellulose (ENCC) and dicarboxylated cellulose (DCC). The aldehyde content of SNCC and consequently surface charge of ENCC (carboxyl content) were precisely controlled by controlling the periodate oxidation reaction time, resulting in highly stable nanoparticles bearing more than 7 mmol functional groups per gram of nanoparticles (e.g., as compared to conventional NCC bearing &#60;&#60; 1 mmol functional group/g). Atomic force microscopy (AFM), transmission electron microscopy (TEM), and scanning electron microscopy (SEM) attested to the rod-like morphology. Conductometric titration, Fourier transform infrared spectroscopy (FTIR), nuclear magnetic resonance (NMR), dynamic light scattering (DLS), electrokinetic-sonic-amplitude (ESA) and acoustic attenuation spectroscopy shed light on the superior properties of these nanomaterials.

Synthesis schemes to prepare highly stable wood fiber-based hairy nanoparticles and functional cellulose-based biopolymers have been detailed.

Nanoparticles, as one of the key materials in nanotechnology and nanomedicine, have gained significant importance during the past decade. While ...

From Molecules to Materials: Engineering New Ionic Liquid Crystals Through Halogen Bonding

Herein, we demonstrate that a bottom-up approach, based on halogen bonding (XB), can be successfully applied for the design of a new type of ionic liquid crystals (ILCs). Taking advantages of the high specificity of XB for haloperfluorocarbons and the ability of anions to act as XB-acceptors, we obtained supramolecular complexes based on 1-alkyl-3-methylimidazolium iodides and iodoperfluorocarbons, overcoming the well-known immiscibility between hydrocarbons (HCs) and perfluorocarbons (PFCs). The high directionality of the XB combined with the fluorophobic effect, allowed us to obtain enantiotropic liquid crystals where a rigid, non-aromatic, XB supramolecular anion acts as mesogenic core.
X-ray structure analysis of the complex between 1-ethyl-3-methylimidazolium iodide and iodoperfluorooctane showed the presence of a layered structure, which is a manifestation of the well-known tendency to segregation of perfluoroalkyl chains. This is consistent with the observation of smectic mesophases. Moreover, all the reported complexes melt below 100 &#176;C, and most are mesomorphic even at room temperature, despite that the starting materials were non-mesomorphic in nature.
The supramolecular strategy reported here provides new design principles for mesogen design allowing a totally new class of functional materials.

A protocol for the synthesis of a new type of mesogens, based on the halogen-bonded supramolecular anion [CnF2n+1-I&#183;&#183;&#183;I&#183;&#183;&#183;I-CnF2n+1]&#8722;, is reported.

Herein, we demonstrate that a bottom-up approach, based on halogen bonding (XB), can be successfully applied for the design of a new type of ionic liquid ...

Facet-to-facet Linking of Shape-anisotropic Colloidal Cadmium Chalcogenide Nanostructures

Here, we describe a protocol that allows for shape-anisotropic cadmium chalcogenide nanocrystals (NCs), such as nanorods (NRs) and tetrapods (TPs), to be covalently and site-specifically linked via their end facets, resulting in polymer-like linear or branched chains. The linking procedure begins with a cation-exchange process in which the end facets of the cadmium chalcogenide NCs are first converted to silver chalcogenide. This is followed by the selective removal of ligands at their surface. This results in cadmium chalcogenide NCs with highly reactive silver chalcogenide end facets that spontaneously fuse upon contact with each other, thereby establishing an interparticle facet-to-facet attachment. Through the judicious choice of precursor concentrations, an extensive network of linked NCs can be produced. Structural characterization of the linked NCs is carried out via low- and high-resolution transmission electron microscopy (TEM), as well as energy-dispersive X-ray spectroscopy, which confirm the presence of silver chalcogenide domains between chains of cadmium chalcogenide NCs.

A protocol detailing how shape-anisotropic colloidal cadmium chalcogenide nanocrystals can be covalently linked via their end facets is presented here.

Here, we describe a protocol that allows for shape-anisotropic cadmium chalcogenide nanocrystals (NCs), such as nanorods (NRs) and tetrapods (TPs), to be ...

DNA-magnetic Particle Binding Analysis by Dynamic and Electrophoretic Light Scattering

Isolation of DNA using magnetic particles is a field of high importance in biotechnology and molecular biology research. This protocol describes the evaluation of DNA-magnetic particles binding via dynamic light scattering (DLS) and electrophoretic light scattering (ELS). Analysis by DLS provides valuable information on the physicochemical properties of particles including particle size, polydispersity, and zeta potential. The latter describes the surface charge of the particle which plays major role in electrostatic binding of materials such as DNA. Here, a comparative analysis exploits three chemical modifications of nanoparticles and microparticles and their effects on DNA binding and elution. Chemical modifications by branched polyethylenimine, tetraethyl orthosilicate and (3-aminopropyl)triethoxysilane are investigated. Since DNA exhibits a negative charge, it is expected that zeta potential of particle surface will decrease upon binding of DNA. Forming of clusters should also affect particle size. In order to investigate the efficiency of these particles in isolation and elution of DNA, the particles are mixed with DNA in low pH (~6), high ionic strength and dehydration environment. Particles are washed on magnet and then DNA is eluted by Tris-HCl buffer (pH = 8). DNA copy number is estimated using quantitative polymerase chain reaction (PCR). Zeta potential, particle size, polydispersity and quantitative PCR data are evaluated and compared. DLS is an insightful and supporting method of analysis that adds a new perspective to the process of screening of particles for DNA isolation.

This protocol describes the synthesis of magnetic particles and evaluation of their DNA-binding properties via dynamic and electrophoretic light scattering. This method focuses on monitoring changes in particle size, their polydispersity and zeta potential of particle surface which play major role in binding of materials such as DNA.

Isolation of DNA using magnetic particles is a field of high importance in biotechnology and molecular biology research. This protocol describes the ...