| Literature DB >> 33431663 |
Yayao Ma1,2, Youngjae Lee1,3, Catherine Best-Popescu1,3, Liang Gao4,2.
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.Entities:
Keywords: FLIM; compressed imaging; high-speed
Mesh:
Year: 2021 PMID: 33431663 PMCID: PMC7826382 DOI: 10.1073/pnas.2004176118
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 12.779