Abstract
We present high-resolution, high-speed fluorescence lifetime imaging microscopy (FLIM) of live cells based on a compressed sensing scheme. By leveraging the compressibility of biological scenes in a specific domain, we simultaneously record the time-lapse fluorescence decay upon pulsed laser excitation within a large field of view. The resultant system, referred to as compressed FLIM, can acquire a widefield fluorescence lifetime image within a single camera exposure, eliminating the motion artifact and minimizing the photobleaching and phototoxicity. The imaging speed, limited only by the readout speed of the camera, is up to 100 Hz. We demonstrated the utility of compressed FLIM in imaging various transient dynamics at the microscopic scale.
Funder
HHS | NIH | National Eye Institute
HHS | NIH | National Institute of General Medical Sciences
HHS | NIH | National Institute of Biomedical Imaging and Bioengineering
NSF | ENG | Division of Chemical, Bioengineering, Environmental, and Transport Systems
Publisher
Proceedings of the National Academy of Sciences
Cited by
40 articles.
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