Programming DNA origami patterning with non-canonical DNA-based metallization reactions

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作者
Sisi Jia
Jianbang Wang
Mo Xie
Jixue Sun
Huajie Liu
Yinan Zhang
Jie Chao
Jiang Li
Lihua Wang
Jianping Lin
Kurt V. Gothelf
Chunhai Fan
机构
[1] Shanghai Jiao Tong University,School of Chemistry and Chemical Engineering, and Institute of Molecular Medicine, Renji Hospital, School of Medicine
[2] Chinese Academy of Sciences,Division of Physical Biology, CAS Key Laboratory of Interfacial Physics and Technology, Shanghai Synchrotron Radiation Facility, Shanghai Institute of Applied Physics
[3] Nankai University,State Key Laboratory of Medicinal Chemical Biology and College of Pharmacy
[4] Tongji University,School of Chemical Science and Engineering, Shanghai Research Institute for Intelligent Autonomous Systems, Key Laboratory of Advanced Civil Engineering Materials of Ministry of Education
[5] Nanjing University of Posts & Telecommunications,Key Laboratory for Organic Electronics & Information Displays (KLOEID), Institute of Advanced Materials (IAM) and School of Materials Science and Engineering
[6] Chinese Academy of Sciences,Zhangjiang Laboratory, Shanghai Advanced Research Institute
[7] East China Normal University,Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering
[8] Aarhus University,Center for DNA Nanotechnology (CDNA) at the Interdisciplinary Nanoscience Center (iNANO) and the Department of Chemistry
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摘要
The inherent specificity of DNA sequence hybridization has been extensively exploited to develop bioengineering applications. Nevertheless, the structural potential of DNA has been far less explored for creating non-canonical DNA-based reactions. Here we develop a DNA origami-enabled highly localized metallization reaction for intrinsic metallization patterning with 10-nm resolution. Both theoretical and experimental studies reveal that low-valence metal ions (Cu2+ and Ag+) strongly coordinate with DNA bases in protruding clustered DNA (pcDNA) prescribed on two-dimensional DNA origami, which results in effective attraction within flexible pcDNA strands for site-specific pcDNA condensation. We find that the metallization reactions occur selectively on prescribed sites while not on origami substrates. This strategy is generically applicable for free-style metal painting of alphabet letters, digits and geometric shapes on all−DNA substrates with near-unity efficiency. We have further fabricated single- and double-layer nanoscale printed circuit board (nano-PCB) mimics, shedding light on bio-inspired fabrication for nanoelectronic and nanophotonic applications.
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