Self-assembly of DNA into nanoscale three-dimensional shapes.

Nature

Department of Cancer Biology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts 02115, USA.

Published: May 2009

AI Article Synopsis

  • Molecular self-assembly, particularly using DNA, allows for the creation of complex structures with incredibly precise dimensions from simple components.
  • Researchers have successfully utilized a method involving a scaffold strand and staple strands to form custom two-dimensional shapes, and they have now extended this approach to design three-dimensional structures on a honeycomb lattice.
  • The study demonstrates the assembly of various nanoshapes, highlights the importance of proper assembly conditions like folding time and ion concentrations, and suggests that this technique could lead to the production of advanced nanotechnology devices.

Article Abstract

Molecular self-assembly offers a 'bottom-up' route to fabrication with subnanometre precision of complex structures from simple components. DNA has proved to be a versatile building block for programmable construction of such objects, including two-dimensional crystals, nanotubes, and three-dimensional wireframe nanopolyhedra. Templated self-assembly of DNA into custom two-dimensional shapes on the megadalton scale has been demonstrated previously with a multiple-kilobase 'scaffold strand' that is folded into a flat array of antiparallel helices by interactions with hundreds of oligonucleotide 'staple strands'. Here we extend this method to building custom three-dimensional shapes formed as pleated layers of helices constrained to a honeycomb lattice. We demonstrate the design and assembly of nanostructures approximating six shapes-monolith, square nut, railed bridge, genie bottle, stacked cross, slotted cross-with precisely controlled dimensions ranging from 10 to 100 nm. We also show hierarchical assembly of structures such as homomultimeric linear tracks and heterotrimeric wireframe icosahedra. Proper assembly requires week-long folding times and calibrated monovalent and divalent cation concentrations. We anticipate that our strategy for self-assembling custom three-dimensional shapes will provide a general route to the manufacture of sophisticated devices bearing features on the nanometre scale.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2688462PMC
http://dx.doi.org/10.1038/nature08016DOI Listing

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