FLIM FRET technology for drug discovery: automated multiwell-plate high-content analysis, multiplexed readouts and application in situ

Chemphyschem. 2011 Feb 25;12(3):609-26. doi: 10.1002/cphc.201000874. Epub 2011 Feb 17.

Abstract

A fluorescence lifetime imaging (FLIM) technology platform intended to read out changes in Förster resonance energy transfer (FRET) efficiency is presented for the study of protein interactions across the drug-discovery pipeline. FLIM provides a robust, inherently ratiometric imaging modality for drug discovery that could allow the same sensor constructs to be translated from automated cell-based assays through small transparent organisms such as zebrafish to mammals. To this end, an automated FLIM multiwell-plate reader is described for high content analysis of fixed and live cells, tomographic FLIM in zebrafish and FLIM FRET of live cells via confocal endomicroscopy. For cell-based assays, an exemplar application reading out protein aggregation using FLIM FRET is presented, and the potential for multiple simultaneous FLIM (FRET) readouts in microscopy is illustrated.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line
  • Drug Evaluation, Preclinical
  • Fluorescence Resonance Energy Transfer / methods*
  • Fluorescent Dyes / chemistry
  • Green Fluorescent Proteins / chemistry
  • Humans
  • Microscopy, Fluorescence
  • Protein Binding
  • Proteins / analysis*
  • Rhodamines / chemistry
  • gag Gene Products, Human Immunodeficiency Virus / analysis

Substances

  • Fluorescent Dyes
  • Proteins
  • Rhodamines
  • gag Gene Products, Human Immunodeficiency Virus
  • rhodamine 6G
  • Green Fluorescent Proteins
  • rhodamine B