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DNA-programmable nanoparticle crystallization

Author

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  • Sung Yong Park

    (Northwestern University, 2145 Sheridan Road, Evanston, Illinois 60208-3113, USA
    Present address: Department of Biostatistics and Computational Biology, University of Rochester, 601 Elmwood Avenue, Rochester, New York 14642, USA.)

  • Abigail K. R. Lytton-Jean

    (Northwestern University, 2145 Sheridan Road, Evanston, Illinois 60208-3113, USA)

  • Byeongdu Lee

    (Advanced Photon Source, Argonne National Laboratory)

  • Steven Weigand

    (DND-CAT Synchrotron Research Center, Northwestern University, APS/ANL 432-A004, 9700 S. Cass Avenue, Argonne, Illinois 60439, USA)

  • George C. Schatz

    (Northwestern University, 2145 Sheridan Road, Evanston, Illinois 60208-3113, USA)

  • Chad A. Mirkin

    (Northwestern University, 2145 Sheridan Road, Evanston, Illinois 60208-3113, USA)

Abstract

DNA rules The idea that DNA base pairing could direct the crystallization of useful materials is a tempting one for nanotechnologists. Now — over ten years after it was first shown that DNA attached to nanoparticles can influence their assembly — two groups have put this concept into practice. Park et al. demonstrate that the DNA molecules attached to gold nanoparticles, and DNA molecules used to link them, can be selected to ensure that the nanoparticles self-assemble into either face-centred cubic or body-centred cubic crystals. The cover graphic, by Cole Krumbholz, is a close-up of the latter. Nykypanchuk et al. identify the requirements for DNA design and the crystallization conditions that allow the reversible formation of body-centred cubic crystals, with nanoparticles occupying just a few percent of a lattice volume. As discussed in News & Views, these developments might make it possible to create ordered and tunable 3D nanoscale architectures relevant for photonic and magnetic applications, biomedical sensing, and information or energy storage.

Suggested Citation

  • Sung Yong Park & Abigail K. R. Lytton-Jean & Byeongdu Lee & Steven Weigand & George C. Schatz & Chad A. Mirkin, 2008. "DNA-programmable nanoparticle crystallization," Nature, Nature, vol. 451(7178), pages 553-556, January.
    • Handle: RePEc:nat:nature:v:451:y:2008:i:7178:d:10.1038_nature06508
    DOI: 10.1038/nature06508
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    Cited by:

    1. Chad R. Simmons & Tara MacCulloch & Miroslav Krepl & Michael Matthies & Alex Buchberger & Ilyssa Crawford & Jiří Šponer & Petr Šulc & Nicholas Stephanopoulos & Hao Yan, 2022. "The influence of Holliday junction sequence and dynamics on DNA crystal self-assembly," Nature Communications, Nature, vol. 13(1), pages 1-9, December.
    2. H. Dehne & A. Reitenbach & A. R. Bausch, 2021. "Reversible and spatiotemporal control of colloidal structure formation," Nature Communications, Nature, vol. 12(1), pages 1-9, December.
    3. Tyler G Moore & Max H Garzon & Russell J Deaton, 2015. "Probabilistic Analysis of Pattern Formation in Monotonic Self-Assembly," PLOS ONE, Public Library of Science, vol. 10(9), pages 1-23, September.
    4. Fan Cui & Sophie Marbach & Jeana Aojie Zheng & Miranda Holmes-Cerfon & David J. Pine, 2022. "Comprehensive view of microscopic interactions between DNA-coated colloids," Nature Communications, Nature, vol. 13(1), pages 1-10, December.
    5. Nam Heon Cho & Young Bi Kim & Yoon Young Lee & Sang Won Im & Ryeong Myeong Kim & Jeong Won Kim & Seok Daniel Namgung & Hye-Eun Lee & Hyeohn Kim & Jeong Hyun Han & Hye Won Chung & Yoon Ho Lee & Jeong W, 2022. "Adenine oligomer directed synthesis of chiral gold nanoparticles," Nature Communications, Nature, vol. 13(1), pages 1-10, December.

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