4.5 Article

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

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JOURNAL OF BIOMEDICAL OPTICS
卷 11, 期 3, 页码 -

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SPIE-INT SOCIETY OPTICAL ENGINEERING
DOI: 10.1117/1.2208999

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fluorescence lifetime; lock-in imaging; microscopy; screening

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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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