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    DNA and DNAzyme-Mediated 2D Colloidal Assembly
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    Beckman Institute, Department of Materials Science and Engineering, and Department of Chemistry, University of Illinois at Urbana−Champaign, 405 North Mathews Avenue, Urbana, Illinois 61801
    [email protected]
    †Beckman Institute.
    ‡Department of Materials Science and Engineering.
    §Department of Chemistry.
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    Journal of the American Chemical Society

    Cite this: J. Am. Chem. Soc. 2008, 130, 26, 8234–8240
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    https://doi.org/10.1021/ja711026r
    Published June 10, 2008
    Copyright © 2008 American Chemical Society
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    Abstract

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    DNA-mediated interactions present a significant opportunity for controlling colloidal self-assembly. Using microcontact printing to achieve spatial control of DNA-surface patterning and DNA-functionalized polystyrene colloids, we report that DNA hybridization can be utilized for sequence-specific reversible self-assembly of well-ordered 2D colloidal arrays. Two essential indicators of DNA-hybridization mediated assembly were confirmed: thermal reversibility and sequence specificity. The arrays melted at 50 °C and reassembled when introduced to fresh colloid suspension, and sequence specificity with <1% nonspecific binding was confirmed using fluorescent polystyrene colloids. The real-time assembly of the colloids onto the periodically patterned substrate was monitored by simple laser diffraction to obtain assembly kinetics. Maximum surface coverage of DNA-mediated assembly was determined to be 0.593 for DNA-functionalized 100 nm polystyrene colloids, and 90% of the assembly was complete after 6.25 h of hybridization in 50 mM NaCl Tris buffer. We also demonstrate that DNAzymes, catalytic DNA molecules, can be incorporated into the design, and in the presence of 10 µM Pb2+, the hybridization-induced array assembly can be disrupted via DNAzyme activity.

    Copyright © 2008 American Chemical Society

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    This article is cited by 31 publications.

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    Journal of the American Chemical Society

    Cite this: J. Am. Chem. Soc. 2008, 130, 26, 8234–8240
    Click to copy citationCitation copied!
    https://doi.org/10.1021/ja711026r
    Published June 10, 2008
    Copyright © 2008 American Chemical Society
    Request reuse permissions

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