UNMIX-ME: spectral and lifetime fluorescence unmixing via deep learning.
Jason T SmithMarien OchoaXavier IntesPublished in: Biomedical optics express (2020)
Hyperspectral fluorescence lifetime imaging allows for the simultaneous acquisition of spectrally resolved temporal fluorescence emission decays. In turn, the acquired rich multidimensional data set enables simultaneous imaging of multiple fluorescent species for a comprehensive molecular assessment of biotissues. However, to enable quantitative imaging, inherent spectral overlap between the considered fluorescent probes and potential bleed-through must be considered. Such a task is performed via either spectral or lifetime unmixing, typically independently. Herein, we present "UNMIX-ME" (unmix multiple emissions), a deep learning-based fluorescence unmixing routine, capable of quantitative fluorophore unmixing by simultaneously using both spectral and temporal signatures. UNMIX-ME was trained and validated using an in silico framework replicating the data acquisition process of a compressive hyperspectral fluorescent lifetime imaging platform (HMFLI). It was benchmarked against a conventional LSQ method for tri and quadri-exponential simulated samples. Last, UNMIX-ME's potential was assessed for NIR FRET in vitro and in vivo preclinical applications.
Keyphrases
- single molecule
- high resolution
- living cells
- deep learning
- fluorescent probe
- optical coherence tomography
- energy transfer
- quantum dots
- fluorescence imaging
- artificial intelligence
- stem cells
- gene expression
- big data
- small molecule
- photodynamic therapy
- mesenchymal stem cells
- convolutional neural network
- computed tomography
- label free
- heavy metals
- sensitive detection
- dual energy
- molecular dynamics simulations
- drug release
- sewage sludge
- municipal solid waste