Mario González-Gutiérrez, Diana M. Vázquez-Enciso, Nicolás Mateos, Wonsang Hwang, Esley Torres-García, Haydee O. Hernández, Jenu V. Chacko, Iván Coto Hernández, Pablo Loza-Álvarez, Christopher Wood, Adan Guerrero
{"title":"PSF-Driven Spatiotemporal Blending in Fluorescence Lifetime Imaging Microscopy and Its Mitigation via Mean-Shift Super-Resolution-Based Masking","authors":"Mario González-Gutiérrez, Diana M. Vázquez-Enciso, Nicolás Mateos, Wonsang Hwang, Esley Torres-García, Haydee O. Hernández, Jenu V. Chacko, Iván Coto Hernández, Pablo Loza-Álvarez, Christopher Wood, Adan Guerrero","doi":"10.1021/acsphotonics.6c00741","DOIUrl":null,"url":null,"abstract":"<p>Fluorescence lifetime imaging microscopy (FLIM) enables\r\nquantitative\r\nmapping of molecular environments in living systems with high biochemical\r\nspecificity. However, spatial overlap dictated by the diffraction-limited\r\npoint spread function (PSF) causes a mixing of temporal signals: photons\r\nfrom neighboring emitters collected within the same pixel yield composite\r\ndecay profiles, generating apparent intermediate lifetimes that can\r\nbe mistaken for variations in the local molecular environment. We\r\nintroduce a workflow that applies mean-shift super-resolution (MSSR)\r\nto raw intensity data to generate intensity-derived spatial masks\r\nprior to phasor-based lifetime analysis. The method is computationally\r\nefficient and preserves decay kinetics because it operates on intensity-derived\r\nspatial information rather than modifying temporal data. In U2OS cells\r\nlabeled with spectrally-overlapping fluorophores, phasor analysis\r\nreveals an intermediate lifetime population localized at PSF-overlap\r\ninterfaces, consistent with optical mixing rather than intrinsic lifetime\r\nheterogeneity. MSSR-derived masking suppressed this mixed population\r\nwhile preserving the distribution of similar phasor coordinates in\r\nthe phasor plane for each fluorophore. Simulations of strictly monoexponential\r\nfluorescence decay emitters further show that blended lifetime decay\r\nprofiles are present at separations up to 4σ, indicating that\r\nconventional spatial resolution criteria can underestimate lifetime\r\ncross-talk. Application of this workflow to three-component FLIM showed\r\nalso a reduced overlap of pixel distributions in phasor plots while\r\nmaintaining distinct lifetime signatures. Ultimately, the primary\r\nvalue of MSSR-based spatial refinement lies in leveraging improved\r\nspatial resolution to effectively isolate the temporal profiles of\r\nmixed fluorophore populations preserving the integrity of FLIM measurements.</p>","PeriodicalId":23,"journal":{"name":"ACS Photonics","volume":"13 19","pages":"5571–5590"},"PeriodicalIF":6.0000,"publicationDate":"2026-10-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Photonics","FirstCategoryId":"101","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acsphotonics.6c00741","RegionNum":1,"RegionCategory":"物理与天体物理","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/9/14 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
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 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 4σ, 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. Ultimately, the primary
value of MSSR-based spatial refinement lies in leveraging improved
spatial resolution to effectively isolate the temporal profiles of
mixed fluorophore populations preserving the integrity of FLIM measurements.
期刊介绍:
Published as soon as accepted and summarized in monthly issues, ACS Photonics will publish Research Articles, Letters, Perspectives, and Reviews, to encompass the full scope of published research in this field.