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Tailoring DNA structure to increase target hybridization kinetics on surfaces.


ABSTRACT: We report a method for increasing the rate of target hybridization on DNA-functionalized surfaces using a short internal complement DNA (sicDNA) strand. The sicDNA causes up to a 5-fold increase in association rate by inducing a conformational change that extends the DNA away from the surface, making it more available to bind target nucleic acids. The sicDNA-induced kinetic enhancement is a general phenomenon that occurred with all sequences and surfaces investigated. Additionally, the process is selective and can be used in multicomponent systems to controllably and orthogonally "turn on" specific sequences by the addition of the appropriate sicDNA. Finally, we show that sicDNA is compatible with systems used in gene regulation, intracellular detection, and microarrays, suggesting several potential therapeutic, diagnostic, and bioinformatic applications.

SUBMITTER: Prigodich AE 

PROVIDER: S-EPMC3918422 | biostudies-literature | 2010 Aug

REPOSITORIES: biostudies-literature

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Tailoring DNA structure to increase target hybridization kinetics on surfaces.

Prigodich Andrew E AE   Lee One-Sun OS   Daniel Weston L WL   Seferos Dwight S DS   Schatz George C GC   Mirkin Chad A CA  

Journal of the American Chemical Society 20100801 31


We report a method for increasing the rate of target hybridization on DNA-functionalized surfaces using a short internal complement DNA (sicDNA) strand. The sicDNA causes up to a 5-fold increase in association rate by inducing a conformational change that extends the DNA away from the surface, making it more available to bind target nucleic acids. The sicDNA-induced kinetic enhancement is a general phenomenon that occurred with all sequences and surfaces investigated. Additionally, the process i  ...[more]

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