Metallization of double-stranded DNA triggered by bound galactose-modified naphthalene diimide

Bioconjug Chem. 2014 Aug 20;25(8):1547-55. doi: 10.1021/bc500263b. Epub 2014 Jul 23.

Abstract

Naphthalene diimide (NDI) derivatives bearing galactose moieties through different spacers, NDI-DS1 and NDI-DS2, were synthesized by the click reaction of the acetylene derivatives of NDI with galactose azide. They bound to double-stranded DNA with threading intercalation, as confirmed by the topoisomerase I assay and circular dichroism spectroscopy. The binding affinities of these ligands were on the order of 10(5) M(-1) with several-fold higher affinity for double-stranded DNA than for single-stranded DNA. The silver mirror reaction on the double-stranded DNA bound to these ligands afforded silver nanowires that were converted to gold nanowires. In the atomic force microscopy measurements, the increased height of DNA areas on a mica plate was observed in the case of double-stranded DNA after NDI-DS2 treatment and subsequently silver mirror reaction, whereas the increased height of DNA areas was not observed in the case of single-stranded DNA after the same treatment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Click Chemistry
  • DNA / chemistry*
  • DNA, Single-Stranded / chemistry
  • Galactose / chemistry*
  • Imides / chemistry*
  • Models, Molecular
  • Naphthalenes / chemistry*
  • Nucleic Acid Conformation
  • Silver / chemistry*
  • Substrate Specificity

Substances

  • DNA, Single-Stranded
  • Imides
  • Naphthalenes
  • naphthalenediimide
  • Silver
  • DNA
  • Galactose