Single-molecule fluorescence coincidence spectroscopy and its application to resonance energy transfer

Chemphyschem. 2011 Feb 25;12(3):491-9. doi: 10.1002/cphc.201000636. Epub 2010 Oct 4.

Abstract

The use of Förster resonance energy transfer (FRET) as a tool to study biomolecules has been greatly enhanced by new advances in single-molecule fluorescence (SMF) techniques. This has allowed new insights into the structure and dynamics of complex biomolecular machinery. However, there are still technical drawbacks in the application of conventional SMF-FRET. Herein, we review the use of single-molecule coincidence spectroscopy to study FRET systems, an analytical variation of the conventional scheme, using one or two confocal lasers of different colours. We highlight the advantages of the coincidence spectroscopy and illustrate this with examples of its application to some biological systems of interest.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Fluorescence Resonance Energy Transfer / methods*
  • Nucleic Acid Conformation
  • Protein Folding
  • Proteins / chemistry
  • RNA / chemistry
  • Spectrometry, Fluorescence*

Substances

  • Proteins
  • RNA