Fluorescence lifetime imaging microscopy in life sciences

J.W. Borst, A.J.W.G. Visser

Research output: Contribution to journalArticleAcademicpeer-review

106 Citations (Scopus)

Abstract

Fluorescence lifetime imaging microscopy (FLIM) and fluorescence anisotropy imaging microscopy (FAIM) are versatile tools for the investigation of the molecular environment of fluorophores in living cells. Owing to nanometre-scale interactions via Förster resonance energy transfer (FRET), FLIM and FAIM are powerful microscopy methods for the detection of conformational changes and protein–protein interactions reflecting the biochemical status of live cells. This review provides an overview of recent advances in photonics techniques, quantitative data analysis methods and applications in the life sciences
Original languageEnglish
Article number102002
Number of pages21
JournalMeasurement Science and Technology
Volume21
Issue number10
DOIs
Publication statusPublished - 2010

Keywords

  • resonance energy-transfer
  • protein-protein interactions
  • quantitative fret analysis
  • living plant-cells
  • correlation spectroscopy
  • live cells
  • global analysis
  • streak camera
  • modulation fluorometry
  • polarized fluorescence

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