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Design and self-assembly of two-dimensional DNA crystals

Naturevolume 394pages539544 (1998) | Download Citation

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Abstract

Molecular self-assembly presents a ‘bottom-up’ approach to the fabrication of objects specified with nanometre precision. DNA molecular structures and intermolecular interactions are particularly amenable to the design and synthesis of complex molecular objects. We report the design and observation of two-dimensional crystalline forms of DNA that self-assemble from synthetic DNA double-crossover molecules. Intermolecular interactions between the structural units are programmed by the design of ‘sticky ends’ that associate according to Watson–Crick complementarity, enabling us to create specific periodic patterns on the nanometre scale. The patterned crystals have been visualized by atomic force microscopy.

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Acknowledgements

We thank J. Hopfield, S. Roweis, S. Mahajan, C. Brody, L. Adleman and P. Rothemund for discussion; J. Abelson and his group for use of his laboratory and for technical advice; A. Segal, E. Rabani and R. Moision for instruction and advice on AFM imaging; the Beckman Institute Molecular Materials Resource Center for assistance and use of their AFM facilities; F. Furuya for help with labelling; and M. Yoder, V. Morozov, D. Stokes, M. Simon and J. Wall for assistance in early attempts to visualize DNA lattices. The research at Caltech has been supported by the National Institute for Mental Health, General Motors' Technology Research Partnerships program, and by the Center for Neuromorphic Systems Engineering as a part of the NSF Engineering Research Center Program. The research at NYU has been supported by the Office of Naval Research, the National Institute of General Medical Sciences, and the NSF.

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  1. Computation and Neural Systems, California Institute of Technology, Pasadena, 91125, California, USA

    • Erik Winfree
  2. Department of Chemistry, New York University, New York, New York, 10003, USA

    • Furong Liu
    • , Lisa A. Wenzler
    •  & Nadrian C. Seeman

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Correspondence to Erik Winfree.

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https://doi.org/10.1038/28998

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