Method Article

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

DOI:

10.3791/52486

May 8th, 2015

In This Article

Summary

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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.

Abstract

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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.

Introduction

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Previous nucleic acid self-assembly work1-25 has led to the successful construction of a variety of complex structures, including DNA25,8,1013,17,23 or RNA7,22 periodic3,4,7,22 and algorithmic5 two-dimensional lattices, ribbons10,12 and tubes4,12,13, 3D crystals17, polyhedra11 and finite, 2D shapes7,8. A particularly effective method is scaffolded DNA origami, whereby a single scaffold strand is folded by many short auxiliary staple strands to form a complex shape9,1416....

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Protocol

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1. DNA Sequence Design

  1. Use UNIQUIMER software27 to design a SST-finite structure by specifying the number of double helices, lengths of top and bottom helix for each double helix, and the crossover pattern to create a 24H × 28T canvas. After defining these parameters, the overall architecture (strand composition and the complementarity arrangement) is illustrated graphically in the program.
  2. Generate sequences for the strands of the specified structure to meet the complementarity arrangement and additional requirements (if any). Design DNA sequences by minimizing the sequence symmetry28 (for most of the structures).....

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Results

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The self-assembly of SSTs (Figure 1) will yield a 24H × 28T rectangle, as illustrated in Figure 2. DNA sequences for the different SSTs can be modified/optimized to enable streptavidin labeling (Figure 3 and 4), the transformation of a rectangle into a tube (Figure 5), the programmable self-assembly of SSTs to form tubes and rectangles of varying sizes (Figure 10), and the construction of 2D arbitrary shapes using the mo.......

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Discussion

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In the structure formation step, it is important to keep an appropriate concentration of magnesium cations (e.g., 15 mM) in the DNA strand mixture to self-assemble DNA nanostructures. Similarly, in the agarose gel characterization/purification step, it is important to keep an appropriate magnesium cation concentration (e.g., 10 mM) in the gel and the gel running buffer to retain the DNA nanostructures during electrophoresis. For the 24H×28T rectangle structure, we tested annealing in different Mg

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Disclosures

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The authors declare competing financial interests.

Acknowledgements

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This work was funded by the Office of Naval Research Young Investigator Program Award N000141110914, Office of Naval Research Grant N000141010827, NSF CAREER Award CCF1054898, NIH Director’s New Innovator Award 1DP2OD007292 and a Wyss Institute for Biologically Inspired Engineering Faculty Startup Fund (to P.Y.) and Tsinghua-Peking Center for Life Sciences Startup Fund (to B. W.).

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
DNA Strands Integrated DNA TechnologySection 3.1
SYBR Safe DNA gel stainInvitrogenS33102Section 3.4.2
Freeze'N Squeeze DNA Gel Extraction Spin ColumnsBIO-RAD731-6166Section 3.6
Bruker's Sharp Nitride Lever ProbesBruker AFM ProbesSNL10Section 4.3
Safe Imager 2.0 Blue Light TransilluminatorInvitrogenG6600Section 3.6
Centrifuge 5430REppendorf5428 000.414Section 3.6
Transmission Electron Microscope JeolJem 1400Section 7.4
Multimode 8VeecoSection 4
Typhoon FLA 9000 Laser ScannerGE Heathcare Life Sciences28-9558-08Section 3.5
Ultrapure Distilled waterInvitrogen10977-023Section 3.7.1
Mica diskSPI Supplies12001-26-2Section 4.1
Steel mounting diskTed Pella, Inc.16218Section 4.1
carbon coated copper grid for TEMElectron Microscopy SciencesFCF400-CuSection 7.2
tweezersDumont0203-N5AC-POSection 7.31
glow discharge systemQuorum TechnologiesK100XSection 7.2
DNA Engine Tetrad 2 Peltier Thermal CyclerBIO-RADPTC–0240GSection 3.3
Owl Easycast B2 Mini Gel Electrophoresis SystemsThermoScientificB2Section 3.4.3
Seekam LE Agarose 500GLonza50004Section 3.4.1
GeneRuler 1kb Plus DNA Ladder, Ready-To-Use 75-20000bpThermoScientificSM1333Section 3.4.4
Nanodrop 2000c UV-vis SpectrophotometerThermoScientificSection 3.7
0.2 um filterCorning Inc.431219Section 7.1.2

References

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  1. Seeman, N. C. Nucleic acid junctions and lattices. J. Theor. Biol. 99 (2), 237-247 (1982).
  2. Fu, T. J., Seeman, N. C. DNA double-crossover molecules. Biochemistry. 32 (13), 3211-3220 (1993).
  3. Winfree, E., Liu, F., Wenzler, L. A., Seeman, N. C.

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Tags

Single stranded DNA TilesDNA Nanostructure Self assemblyMolecular Canvas AssemblyNative Agarose Gel ElectrophoresisAtomic Force Microscopy ImagingDNA Strand PurificationThermal Cycler AnnealingEdge Protector DesignDomain Substitution MethodDNA Concentration Measurement

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