FLIM FRET Technology for Drug Discovery: Automated Multiwell‐Plate High‐Content Analysis, Multiplexed Readouts and Application in Situ

Sunil Kumar(Imperial College London), Dominic Alibhai(Imperial College London), Anca Margineanu(Imperial College London), Romain F. Laine(Imperial College London), Gordon T. Kennedy(Imperial College London), James McGinty(Imperial College London), Sean Warren(Imperial College London), Douglas J. Kelly(Imperial College London), Yuriy Alexandrov(Imperial College London), Ian Munro(Imperial College London), Clifford Talbot(Imperial College London), Daniel W. Stuckey(Hammersmith Hospital), Christopher Kimberly(Institute of Cancer Research), Bertrand Viellerobe(Mauna Kea Technologies (France)), F. Lacombe(Mauna Kea Technologies (France)), Eric W.‐F. Lam(Imperial College London), Harriet Taylor(Imperial College London), Margaret J. Dallman(Imperial College London), Gordon Stamp(Imperial College London), Edward J. Murray(Pfizer (United Kingdom)), Frank Stühmeier(Pfizer (United Kingdom)), Alessandro Sardini(Hammersmith Hospital), Matilda Katan(Institute of Cancer Research), Daniel S. Elson(NIHR Imperial Biomedical Research Centre), Mark A. A. Neil(Imperial College London), Chris Dunsby(Imperial College London), P. M. W. French(Imperial College London)
ChemPhysChem
February 17, 2011
Cited by 74Open Access
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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.


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