4.8 Article

Control ling Droplet Motion on an Organogel Surface by Tuning the Chain Length of DNA and Its Biosensing Application

Journal

CHEM
Volume 4, Issue 12, Pages 2929-2943

Publisher

CELL PRESS
DOI: 10.1016/j.chempr.2018.09.028

Keywords

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Funding

  1. National Basic Research Program of China (973 Program) [2015CB932600]
  2. National Key RAMP
  3. D Program of China [2017YFA0208000, 2016YFF0100800]
  4. National Natural Science Foundation of China [21525523, 21722507, 21574048, 21874121, 31800829]
  5. Fok Ying-Tong Education Foundation of China [151011]
  6. Natural Science Foundation of Shandong Province [ZR2018BB054]
  7. China Postdoctoral Science Foundation [2017M610492]
  8. open project of the Hubei Key Laboratory of Forensic Science [2018KF001]

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Controllable droplet motion has attracted extensive attention but still faces the challenges of an uncontrollable sliding speed and a slow response rate. Here, controllable sliding speed and critical sliding angle (CSA) of a droplet on an oil-swollen organogel surface are achieved with a fast response rate via modulation of the DNA chain length. Comprehensive investigations ranging from macroscopic wetting behavior to molecular mechanism suggest that short single-stranded DNA (ssDNA) could act as a hydrotrope to interact with oil molecules via interfacial hydrophobic interactions while increasing the interfacial thickness and adhesion, thus hindering the movement of droplets. Conversely, long ssDNA generated from rolling-circle amplification tend toward a curled conformation, minimizing nucleobase exposure and leading to weak interfacial adhesion, allowing the droplets to slide easily. With a significant CSA gradient, biosensing applications for ATP, microRNA, and thrombin detection are demonstrated, indicating the potential for the detection of a broad range of targets.

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