4.8 Article

Silver Nanoclusters Serve as Fluorescent Rivets Linking Hoogsteen Triplex DNA and DNA Structures

Journal

ACS NANO
Volume 16, Issue 8, Pages 13211-13222

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.2c06631

Keywords

Hoogsteen triplex DNA; Nanorivets; Silver nanoclusters; Head-to-head dimerization, and Noncanonical DNA origami

Funding

  1. Korea Research Fellowship Program - Ministry of Science and ICT [NRF 2017H1D3A1A01014182, NRF-2017M2A2A6A04093177]
  2. Korea Health Technology R&D Project through the Korea Health Industry Development Institute (KHIDI) - Ministry of Health & Welfare, Republic of Korea [HU21C0053]
  3. Basic Science Research Program through the National Research Foundation (NRF) - Ministry of Education, Republic of Korea [2018R1A6A1A03025607, 2018R1D1A1B07051125, 2021R1A6A3A13044758, 2022R1F1A1073998]
  4. Brain Korea 21 (BK21) PLUS program
  5. Yonsei University Research Fund [2017-22-0046]
  6. Institute for Basic Science [IBS-R023-D1]
  7. National Research Foundation of Korea [2022R1F1A1073998, 2021R1A6A3A13044758, 2018R1D1A1B07051125] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

Ask authors/readers for more resources

A greater understanding of the interaction between DNA and nanomaterials can provide alternative strategies for designing DNA nanomachines. This study found that the fluorescence of AgNCs encapsulated within DNA can be controlled by pH changes. AgNCs can also act as nanoscale rivets, linking different DNA nanostructures.
Greater understanding of the mutual influence between DNA and the associated nanomaterial on the properties of each other can provide alternative strategies for designing and developing DNA nanomachines. DNA secondary structures are essential for encapsulating highly emissive silver nanoclusters (DNA/AgNCs). Likewise, AgNCs stabilize secondary DNA structures, such as hairpin DNA, duplex DNA, and parallel-motif DNA triplex. In this study, we found that the fluorescence of AgNCs encapsulated within a Hoogsteen triplex DNA structure can be turned on and off in response to pH changes. We also show that AgNCs can act as nanoscale rivets, linking two functionally distinctive DNA nanostructures. For instance, we found that a Hoogsteen triplex DNA structure with a seven-cytosine loop encapsulates red fluorescent AgNCs. The red fluorescence faded under alkaline conditions, whereas the fluorescence was restored in a near-neutral environment. Hairpin DNA and random DNA structures did not exhibit this pH dependent AgNCs fluorescence. A fluorescence lifetime measurement and a small-angle X-ray scattering analysis showed that the triplex DNA-encapsulated AgNCs were photophysically convertible between bright and dark states. An in-gel electrophoresis analysis indicated that bright and dark convertibility depended on the AgNCs-riveted dimerization of the triplex DNAs. Moreover, we found that AgNCs rivet the triplex DNA and hairpin DNA to form a heterodimer, emitting orange fluorescence. Our findings suggest that AgNCs between two cytosine-rich loops can be used as nanorivets in designing noncanonical DNA origami beyond Watson-Crick base pairing.

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