Immobilization of amine-modified oligonucleotides on aldehyde-terminated alkanethiol monolayers on gold

Langmuir. 2005 Jan 4;21(1):266-71. doi: 10.1021/la048166r.

Abstract

Chemistry is described for the fabrication of DNA arrays on gold surfaces. Alkanethiols modified with terminal aldehyde groups are used to prepare a self-assembled monolayer (SAM). The aldehyde groups of the monolayer may be reacted with amine-modified oligonucleotides or other amine-bearing biomolecules to form a Schiff base, which may then be reduced to a stable secondary amine by treatment with sodium cyanoborohydride. The surface modifications and reactions are characterized by polarization modulation Fourier transform infrared reflection absorption spectroscopy (PM-FTIRRAS), and the accessibility, binding specificity, and stability of the DNA-modified surfaces are demonstrated in hybridization experiments.

Publication types

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

MeSH terms

  • Aldehydes / chemistry*
  • Amines / chemistry*
  • Base Sequence
  • Gold / chemistry*
  • Magnetic Resonance Spectroscopy
  • Nucleic Acid Hybridization
  • Oligonucleotides / chemistry*
  • Spectroscopy, Fourier Transform Infrared

Substances

  • Aldehydes
  • Amines
  • Oligonucleotides
  • Gold