ACS PhotonicsBiophysicsPeer-reviewed journal article
PSF-Driven Spatio-Temporal Blending in Fluorescence Lifetime Imaging Microscopy and Its Mitigation via Mean-Shift Super-Resolution-Based Masking.
Mario González-GutiérreziD, Diana M. Vázquez-EncisoiD, Nicolas MateosiD, Wonsang HwangiD, Esley TorresiD, Haydee O. Hernández, Jenu Varghese ChackoiD, Iván Coto HernándeziD, Pablo Loza‐ÁlvareziD, Christopher D. WoodiD, Adan Guerrero
Abstract
Fluorescence Lifetime Imaging Microscopy (FLIM) enables quantitative mapping of molecular environments in living systems with high biochemical specificity. However, spatial overlap dictated by the diffraction-limited point spread function (PSF) causes a mixing of temporal signals: photons from neighboring emitters collected within the same pixel yield composite decay profiles, generating apparent intermediate lifetimes that can be mistaken for variations in the local molecular environment. We introduce a workflow that applies Mean-Shift Super-Resolution (MSSR) to raw intensity data to generate intensity-derived spatial masks prior to phasor-based lifetime analysis. The method is computationally efficient and preserves decay kinetics because it operates on intensity-derived spatial information rather than modifying temporal data. In U2OS cells labeled with spectrally-overlapping fluorophores, phasor analysis reveals an intermediate lifetime population localized at PSF-overlap interfaces, consistent with optical mixing rather than intrinsic lifetime heterogeneity. MSSR-derived masking suppressed this mixed population while preserving stable phasor cluster centers -i.e. the distribution of similar phasor coordinates in the phasor plane- for each fluorophore. Simulations of strictly monoexponential fluorescence decay emitters further show that blended lifetime decay profiles are present at separations up to 4{sigma} and becomes maximal near [~]1.6{sigma}, indicating that conventional spatial resolution criteria can underestimate lifetime cross-talk. Application of this workflow to three-component FLIM showed also a reduced overlap of pixel distributions in phasor plots while maintaining distinct lifetime signatures. Overall, MSSR-based spatial refinement provides an accessible strategy to improve the spatial resolution while maintaining accuracy of FLIM measurements.
- organism: human
- assay: fluorescence / live-cell microscopy
- research focus: cell type annotation
- research focus: clustering
- research focus: spatial domain detection
- approach: deep learning
- approach: statistical model
- Citations
- 1
- FWCI
- 2.74
- Field percentile
- top 8%
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Confocal Laser-Scanning Fluorescence-Lifetime Single-Molecule Localisation Microscopy
J. C. Thiele, D. Helmerich, … J. Enderlein·bioRxiv·Aug 25, 2020
- Simultaneous Spectral Differentiation of Multiple Fluorophores in Super-resolution Imaging Using a Glass Phase Plate
S. I. Fernando, J. T. Martineau, … J. Gerton·bioRxiv·Jul 11, 2022
- Enhancing STED Microscopy via Fluorescence Lifetime Unmixing and Filtering in Two-Species SPLIT-STED
Andréanne Deschênes, Antoine Ollier, … Flavie Lavoie‐Cardinal·Methods in microscopyPeer-reviewed·Dec 15, 2025
- Building Fluorescence Lifetime Maps Photon-by-photon by Leveraging Spatial Correlations
- Doubling the resolution of fluorescence-lifetime single-molecule localization microscopy with image scanning microscopy
N. Radmacher, O. Nevskyi, … J. Enderlein·bioRxiv·Aug 23, 2023
- Nanoscopic resolution within a single imaging frame
Esley Torres, Raúl Pinto‐Cámara, … Adán Guerrero·bioRxiv·Oct 17, 2021