Innovating lifetime microscopy: a compact and simple tool for life sciences, screening, and diagnostics

被引:30
作者
Esposito, Alessandro
Gerritsen, Hans C.
Oggier, Thierry
Lustenberger, Felix
Wouters, Fred S.
机构
[1] European Neurosci Inst, Cell Biophys Grp, D-37073 Gottingen, Germany
[2] Univ Utrecht, Debye Inst, POB 80000, NL-3508 TA Utrecht, Netherlands
关键词
fluorescence lifetime; lock-in imaging; microscopy; screening;
D O I
10.1117/1.2208999
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Fluorescence lifetime imaging microscopy (FLIM) allows the investigation of the physicochemical environment of fluoro-chromes and protein-protein interaction mapping by Forster resonance energy transfer (FRET) in living cells. However, simpler and cheaper solutions are required before this powerful analytical technique finds a broader application in the life sciences. Wide-field frequency-domain FLIM represents a solution whose application is currently limited by the need for multichannel-plate image intensifiers. We recently showed the feasibility of using a charge-coupled device/complementory metal-oxide semiconductor (CCD/CMOS) hybrid lock-in imager, originally developed for 3-D vision, as an add-on device for lifetime measurements on existing wide-field microscopes. In the present work, the performance of the setup is validated by comparison with well-established wide-field frequency-domain FLIM measurements. Furthermore, we combine the lock-in imager with solid-state light sources. This results in a simple, inexpensive, and compact FLIM system, operating at a video rate and capable of single-shot acquisition by virtue of the unique parallel retrieval of two phase-dependent images. This novel FLIM setup is used for cellular and FRET imaging, and for high-throughput and fast imaging applications. The all-solid-state design bridges the technological gap that limits the use of FLIM in areas such as drug discovery and medical diagnostics. (c) 2006 Society of Photo-Optical Instrumentation Engineers.
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页数:8
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