Localized surface plasmon resonance interfaces coated with poly[3-(pyrrolyl)carboxylic acid] for histidine-tagged peptide sensing

Analyst. 2011 Oct 21;136(20):4211-6. doi: 10.1039/c1an15535k. Epub 2011 Aug 26.

Abstract

The paper reports on a novel localized surface plasmon resonance (LSPR) substrate architecture for the immobilization and detection of histidine-tagged peptides. The LSPR interface consists of an ITO (indium tin oxide) substrate coated with gold nanostructures. The latter are obtained by thermal deposition of a thin (2 nm thick) gold film followed by post-annealing at 500 °C. The LSPR interface was coated with poly[3-(pyrrolyl)carboxylic acid] thin films using electrochemical means. The ability of the LSPR interfaces coated with poly[3-(pyrrolyl)carboxylic acid] to chelate copper ions was investigated. Once loaded with metal ions, the modified LSPR interface was able to bind specifically to histidine-tagged peptides. The binding process was followed using LSPR.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biosensing Techniques / methods*
  • Carboxylic Acids / chemistry*
  • Copper / chemistry
  • Gold / chemistry
  • Histidine / chemistry*
  • Metal Nanoparticles / chemistry
  • Oligopeptides / chemistry*
  • Peptides / analysis*
  • Pyrroles / chemistry*
  • Spectrophotometry, Ultraviolet
  • Surface Plasmon Resonance*
  • Tin Compounds / chemistry

Substances

  • Carboxylic Acids
  • His-His-His-His-His-His
  • Oligopeptides
  • Peptides
  • Pyrroles
  • Tin Compounds
  • poly(3-(pyrrolyl)carboxylic acid)
  • Histidine
  • indium tin oxide
  • Gold
  • Copper