4.8 Article

Mechanisms of Surface-Mediated DNA Hybridization

Journal

ACS NANO
Volume 8, Issue 5, Pages 4488-4499

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/nn4064874

Keywords

single molecule; resonance energy transfer; DNA; hybridization; molecular searching

Funding

  1. National Institute of Biomedical Imaging and Bioengineering of the National Institutes of Health [5R21EB015061-02]
  2. National Science Foundation [CHE-1306108]
  3. Division Of Chemistry
  4. Direct For Mathematical & Physical Scien [1306108] Funding Source: National Science Foundation

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Single-molecule total internal reflection fluorescence microscopy was employed in conjunction with resonance energy transfer (RET) to observe the dynamic behavior of donor-labeled ssDNA at the interface between aqueous solution and a solid surface decorated with complementary acceptor-labeled ssDNA. At least 100 000 molecular trajectories were determined for both complementary strands and negative control ssDNA. RET was used to identify trajectory segments corresponding to the hybridized state. The vast majority of molecules from solution adsorbed nonspecifically to the surface, where a brief two-dimensional search was performed with a 7% chance of hybridization. Successful hybridization events occurred with a characteristic search time of similar to 0.1 s, and unsuccessful searches resulted in desorption from the surface, ultimately repeating the adsorption and search process. Hybridization was reversible, and two distinct modes of melting (i.e., dehybridization) were observed, corresponding to long-lived (similar to 15 s) and short-lived (similar to 1.4 s) hybridized time intervals. A strand that melted back onto the surface could rehybridize after a brief search or desorb from the interface. These mechanistic observations provide guidance for technologies that involve DNA interactions in the near-surface region, suggesting a need to design surfaces that both enhance the complex multidimensional search process and stabilize the hybridized state.

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