4.8 Article

Sequence-Dependent DNA Functionalization of Upconversion Nanoparticles and Their Programmable Assemblies

Journal

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 59, Issue 21, Pages 8133-8137

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202000831

Keywords

DNA; nanostructures; poly-cytosine; upconversion nanoparticles; self-assembly

Funding

  1. National Key Research and Development Program of China [2018YFC1106100, 2018YFC1106102]
  2. National Natural Science Foundation of China [21673139, 21661162001, 51973112, 51690151, 51473093, 91956107]

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DNA-modified lanthanide-doped upconversion nanoparticles (DNA-UCNPs) that combine the functions of DNA and the optical features of UCNPs have shown great promise in a wide range of fields. However, challenges remain in precisely tethering and orienting the DNA strands on the UCNP surface. Herein, we systematically investigate the sequence dependence of DNAs in their interactions with UCNPs, and reveal that poly-cytosine (poly-C) has high affinity for the UCNP surface. A general approach to synthesize monodispersed DNA-UCNP conjugates is developed using poly-C-containing diblock DNA strands. The poly-C segment of the DNA strand binds to the surfaces of UCNPs and the second segment is oriented perpendicularly on the UCNP surface, making the DNA-UCNPs highly stable and monodispersed in aqueous solution. The dense layer of DNA on the UCNP surface enables the programmable assembly of UCNPs with other DNA-functionalized nanoparticles or DNA origamis through hybridization, resulting in the formation of well-organized complex structures.

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