Article

Multilayer DNA Origami Packed on a Square Lattice

Department of Chemistry and Biochemistry, and the Biodesign Institute, Arizona State University, Tempe, Arizona 85287, Department of Cancer Biology, Dana-Farber Cancer Institute, and Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts 02115, Wyss Institute for Biologically Inspired Engineering at Harvard, Cambridge, Massachusetts 02138, and National Resource for Automated Molecular Microscopy, The Scripps Research Institute, La Jolla, California 92037
J. Am. Chem. Soc., 2009, 131 (43), pp 15903–15908
DOI: 10.1021/ja906381y
Publication Date (Web): October 6, 2009
Copyright © 2009 American Chemical Society
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Arizona State University.

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Harvard Medical School and Wyss Institute for Biologically Inspired Engineering at Harvard.

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The Scripps Research Institute.

Abstract

Abstract Image

Molecular self-assembly using DNA as a structural building block has proven to be an efficient route to the construction of nanoscale objects and arrays of increasing complexity. Using the remarkable “scaffolded DNA origami” strategy, Rothemund demonstrated that a long single-stranded DNA from a viral genome (M13) can be folded into a variety of custom two-dimensional (2D) shapes using hundreds of short synthetic DNA molecules as staple strands. More recently, we generalized a strategy to build custom-shaped, three-dimensional (3D) objects formed as pleated layers of helices constrained to a honeycomb lattice, with precisely controlled dimensions ranging from 10 to 100 nm. Here we describe a more compact design for 3D origami, with layers of helices packed on a square lattice, that can be folded successfully into structures of designed dimensions in a one-step annealing process, despite the increased density of DNA helices. A square lattice provides a more natural framework for designing rectangular structures, the option for a more densely packed architecture, and the ability to create surfaces that are more flat than is possible with the honeycomb lattice. Thus enabling the design and construction of custom 3D shapes from helices packed on a square lattice provides a general foundational advance for increasing the versatility and scope of DNA nanotechnology.

Experimental methods, gel electrophoresis, sequence designs, and additional TEM images are available free of charge via the Internet at http://pubs.acs.org.

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Received 7 August 2009
Published online 6 October 2009
Published in print 4 November 2009
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