Crystallization of DNA-capped gold nanoparticles in high-concentration, divalent salt environments

Angew Chem Int Ed Engl. 2014 Jan 27;53(5):1316-9. doi: 10.1002/anie.201307113. Epub 2013 Dec 20.

Abstract

The multiparametric nature of nanoparticle self-assembly makes it challenging to circumvent the instabilities that lead to aggregation and achieve crystallization under extreme conditions. By using non-base-pairing DNA as a model ligand instead of the typical base-pairing design for programmability, long-range 2D DNA-gold nanoparticle crystals can be obtained at extremely high salt concentrations and in a divalent salt environment. The interparticle spacings in these 2D nanoparticle crystals can be engineered and further tuned based on an empirical model incorporating the parameters of ligand length and ionic strength.

Keywords: DNA hybridization; DNA nanoparticles; DNA nanotechnology; crystallization; divalent salts.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Base Pairing
  • Crystallization
  • DNA / chemistry*
  • DNA / metabolism
  • Gold / chemistry*
  • Ligands
  • Magnesium Chloride / chemistry
  • Metal Nanoparticles / chemistry*
  • Nucleic Acid Hybridization
  • Osmolar Concentration
  • Salts / chemistry*
  • Sodium Chloride / chemistry

Substances

  • Ligands
  • Salts
  • Magnesium Chloride
  • Sodium Chloride
  • Gold
  • DNA