DNA self-assembly scaled up

Self-assembly processes occur in nature in various forms, from molecular-level protein folding and the formation of lipid bilayers to the establishment of Earth’s entire biological system1. Scientists have long aspired to construct artificial objects using self-assembly to reach the dimensions and complexity of cells or organelles, with the aim of building synthetic cellular machines for research, engineering and medical applications. Four papers25 in this issue address this goal by reporting methods for scaling up the sizes and production of self-assembling, designer nanostructures made from DNA.

The biopolymers DNA, RNA and proteins have all been used as building blocks for the assembly of designer nanoscale architectures, to engineer bioinspired or biomimetic systems that can communicate with each other6 and to regulate the functions of living organisms7. DNA is the most useful nanoscale building block because it has several advantages — especially its programmability, which derives from the predictable and stable pairs that form between bases on complementary DNA strands. Moreover, DNA is structurally stable, the geometrical features of its double helix have been well studied, and it is compatible with other biological molecules, which should allow the construction of ‘hetero-biomaterials’ that have complex functions. Various DNA self-assembly methods (see ref. 8, for example) have been developed for constructing synthetic architectures that exhibit great geometrical complexity and nanoscale accuracy.

One of the milestones in DNA nanotechnology was the invention of DNA origami9. In this technique, long, single-stranded DNA is folded into target shapes with the help of hundreds of short DNA strands called staples. The staple strands are designed to be complementary to particular regions of the long DNA, and thereby guide the folding process. A wide variety of 2D and 3D nano-objects has been made using this technique. Many of these are fully addressable10; that is, they can be modified at selected positions, as needed for future applications. However, the size of individual DNA origami nanostructures is limited by the length of the scaffold DNA from which they are built. For example, one widely used scaffold is a genomic DNA approximately 7,200 nucleotides long9, which folds into origami structures no more than 100 nanometres in diameter9,10.

Another important design strategy in DNA nanotechnology is single-stranded tile (SST) assembly11, in which SSTs — nanometre-scale 2D rectangles or 3D bricks, formed from single-stranded DNA — are designed to interlock with each other through the formation of DNA duplexes at their interfaces. Collections of SSTs are used to form 2D sheets or 3D blocks that can be selectively ‘sculpted’ to create different patterns and shapes, simply by including or omitting specific SSTs12. But the sizes of the DNA structures produced in this way are generally comparable to the sizes of origami nanostructures; larger structures have been prepared only in low yields. The papers reported in this issue build on the SST and origami strategies to make micrometre-sized structures, and to scale up the amounts that can be produced.

Tikhomirov et al.2 (page 67) used square DNA origami decorated with surface patterns (formed by DNA strands that extend from the origami surface) as building units to create 2D DNA origami arrays up to about half a micrometre across (Fig. 1a). The square origami join together through the formation of short DNA duplexes at their interfaces. To program the interactions between the square origami, the authors developed a fractal method in which local assembly rules were used recursively in a hierarchical, multi-step process that assembles increasingly large arrays of the square origami. Tikhomirov and colleagues also produced design software called FracTile Compiler, which will enable non-experts to devise DNA sequences and experimental procedures to make large DNA patterns. The authors validated this automated design process by using it to make several DNA ‘pictures’, including the Mona Lisa, a rooster and a chess-game pattern (see Fig. 3 of the paper2).

Figure 1 | Methods for making micrometre-scale DNA objects.a, Tikhomirov et al.2 used DNA origami — a technique in which small DNA strands (staples) guide the self-assembly of a longer strand — to prepare squares. These squares were assembled into 8 × 8 arrays that had customized surface patterns. b, Wagenbauer et al.3 prepared a 3D, V-shaped building block using DNA origami, and assembled this hierarchically into polyhedra. c, Ong et al.4 built on a method known as single-stranded tile assembly to prepare DNA bricks that form one strand that contains 52 nucleotides. Each strand contains four binding domains that enable the bricks to assemble into larger constructions. Thousands of bricks can be programmed to self-assemble into a cuboid that contains a complex cavity.

Wagenbauer et al.3 (page 78) have made 3D DNA origami structures at sizes up to the micrometre scale, using another hierarchical self-assembly approach (Fig. 1b). They used a V-shaped DNA origami object as the basic building block, in which the angle of the V could be altered. By controlling the geometry and interactions between the building blocks, higher-order assemblies can be constructed. The authors demonstrated the capabilities of their method by constructing micrometre-long tubes (similar in size to some bacteria) out of stacked planar rings up to 350 nm in diameter, and three types of polyhedron up to 450 nm in diameter.

Ong et al.4 (page 72) report a method that allows 3D SST DNA constructs to be made at the micrometre scale (Fig. 1c). By extending the principles of first-generation SST systems, the authors designed a brick-shaped DNA building block composed of 52 nucleotides, which contains four 13-nucleotide binding domains. These domains enable the bricks to assemble into larger constructions. Compared with the first-generation bricks (which contained four binding domains, each composed of eight nucleotides), the longer binding domains of the DNA bricks provide better yields and stabilities for large assembled structures. The authors developed software called Nanobricks to design the brick strands needed to make target 3D objects, and used it to plan the synthesis of a set of different complex architectures (see Fig. 3 of the paper4).

Praetorius et al.5 (who belong to the same research group as Wagenbauer and colleagues; page 84) report biotechnology that should greatly reduce the cost of the hundreds of staple strands that are usually used to make DNA origami. They use viruses known as bacteriophages to produce single-stranded precursor DNA that contains hundreds of staple-strand sequences. These sequences are separated by a ‘DNAzyme’ sequence that cleaves itself; the cleavage products then self-assemble into designated DNA origami shapes. Remarkably, the authors’ method reduces the cost of the folded DNA origami structures from about US$200 per milligram to around 20 cents. This strategy will enable scalable and efficient mass production of DNA origami and SST structures, thus enabling large-scale applications, such as therapeutics, drug-delivery systems and nanoelectronic devices.

The papers also offer solutions for long-standing challenges in the field of biomolecular engineering, providing low-cost methods for fabricating self-assembled structures from smaller building blocks, at sizes that can be integrated into objects made using complementary ‘top-down’ techniques (those that carve structures out of bulk material). Furthermore, the reported DNA structures are large enough to enable the production of devices that interact with cells for therapeutic applications, or to make sophisticated molecular machines and assembly lines that make synthetic polymers or program cell–cell interactions. Such self-assembled structures might even be used in synthetic organelles to create systems that sense, monitor and regulate biological processes in living cells.

Nature 552, 34-35 (2017)

doi: https://doi.org/10.1038/d41586-017-07690-y


  1. 1.

    Whitesides, G. M. & Grzybowski, B. Science 295, 2418–2421 (2002).

    PubMed  Article  CAS  Google Scholar 

  2. 2.

    Tikhomirov, G. et al. Nature 552, 67–71 (2017).

    Article  Google Scholar 

  3. 3.

    Wagenbauer, K. F. et al. Nature 552, 78–83 (2017).

    Article  Google Scholar 

  4. 4.

    Ong, L. L. et al. Nature 552, 72–77 (2017).

    Article  Google Scholar 

  5. 5.

    Praetorius, F. et al. Nature 552, 84–87 (2017).

    Article  Google Scholar 

  6. 6.

    Chen, Y.-J., Groves, B., Muscat, R. A. & Seelig, G. Nature Nanotechnol. 10, 748–760 (2015).

    PubMed  Article  CAS  Google Scholar 

  7. 7.

    Li, J., Green, A. A., Yan, H. & Fan, C. Nature Chem. 9, 1056–1067 (2017).

    PubMed  Article  CAS  Google Scholar 

  8. 8.

    Zheng, J. et al. Nature 461, 74–77 (2009).

    PubMed  Article  CAS  Google Scholar 

  9. 9.

    Rothemund, P. W. K. Nature 440, 297–302 (2006).

    PubMed  Article  CAS  Google Scholar 

  10. 10.

    Douglas, S. M. et al. Nature 459, 414–418 (2009).

    PubMed  Article  CAS  Google Scholar 

  11. 11.

    Wei, B., Dai, M. & Yin, P. Nature 485, 623–626 (2012).

    PubMed  Article  CAS  Google Scholar 

  12. 12.

    Ke, Y., Ong, L. L., Shih, W. M. & Yin, P. Science 338, 1177–1183 (2012).

    PubMed  Article  CAS  Google Scholar 

Download references


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