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ssDNA-amphiphile architecture used to control dimensions of DNA nanotubes.

Huihui KuangThomas E Gartner IiiMatheus Dorneles de MelloJun GuoXiao-Bing ZuoMichael TsapatsisArthi JayaramanEfrosini Kokkoli
Published in: Nanoscale (2019)
Controlling the dimensions of DNA nanotubes is of great interest as they can be used in different applications ranging from functional elements in nanodevices to carriers for drug delivery. ssDNA-amphiphiles composed of a ssDNA headgroup, a hydrophobic dialkyl tail and a polycarbon spacer between the tail and the headgroup, self-assemble into hollow DNA nanotubes by forming bilayer nanotapes that transition from twisted nanotapes, to helical nanotapes, to nanotubes. The presence of the DNA nanotubes is verified via cryo-TEM and SAXS. We further explore the effect of the ssDNA secondary structure and tail length on the assembly of the ssDNA-amphiphiles. We demonstrate that the presence of intermolecular G-quadruplexes in the ssDNA sequence dictates the nanotube length. The nanotube diameter is controlled by the hydrophobic tail length, and coarse-grained molecular dynamics simulations are employed to elucidate the tail design impact on assembly.
Keyphrases
  • molecular dynamics simulations
  • circulating tumor
  • cell free
  • single molecule
  • drug delivery
  • molecular dynamics
  • nucleic acid
  • ionic liquid
  • molecular docking
  • circulating tumor cells
  • electron microscopy
  • drug release