Super-resolution Live-cell Fluorescence Lifetime Imaging

Fuente: arXiv
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Bibliographic Details
Main Authors: Marchand, Raphaël, Ortkrass, Henning, Aziz, Daniel, Pfanner, Franz, Abbas, Eman, Rizzoli, Silvio O., Hübner, Wolfgang, Bowman, Adam, Huser, Thomas, Juffmann, Thomas
Format: Preprint
Published: 2025
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author Marchand, Raphaël
Ortkrass, Henning
Aziz, Daniel
Pfanner, Franz
Abbas, Eman
Rizzoli, Silvio O.
Hübner, Wolfgang
Bowman, Adam
Huser, Thomas
Juffmann, Thomas
author_facet Marchand, Raphaël
Ortkrass, Henning
Aziz, Daniel
Pfanner, Franz
Abbas, Eman
Rizzoli, Silvio O.
Hübner, Wolfgang
Bowman, Adam
Huser, Thomas
Juffmann, Thomas
contents Super-resolution Structured Illumination Microscopy (SR-SIM) enables fluorescence microscopy beyond the diffraction limit at high frame rates. Compared to other super-resolution microscopy techniques, the low photon fluence used in SR-SIM makes it readily compatible with live-cell imaging. Here, we combine SR-SIM with electro-optic fluorescence lifetime imaging (EOFLIM), adding the capability of monitoring physicochemical parameters with 156 nm spatial resolution at high frame rate for live-cell imaging. We demonstrate that our new SIMFLIM technique enables super-resolved multiplexed imaging of spectrally overlapping fluorophores, environmental sensing, and live-cell imaging.
format Preprint
id arxiv_https___arxiv_org_abs_2502_16672
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle Super-resolution Live-cell Fluorescence Lifetime Imaging
Marchand, Raphaël
Ortkrass, Henning
Aziz, Daniel
Pfanner, Franz
Abbas, Eman
Rizzoli, Silvio O.
Hübner, Wolfgang
Bowman, Adam
Huser, Thomas
Juffmann, Thomas
Optics
Super-resolution Structured Illumination Microscopy (SR-SIM) enables fluorescence microscopy beyond the diffraction limit at high frame rates. Compared to other super-resolution microscopy techniques, the low photon fluence used in SR-SIM makes it readily compatible with live-cell imaging. Here, we combine SR-SIM with electro-optic fluorescence lifetime imaging (EOFLIM), adding the capability of monitoring physicochemical parameters with 156 nm spatial resolution at high frame rate for live-cell imaging. We demonstrate that our new SIMFLIM technique enables super-resolved multiplexed imaging of spectrally overlapping fluorophores, environmental sensing, and live-cell imaging.
title Super-resolution Live-cell Fluorescence Lifetime Imaging
topic Optics
url https://arxiv.org/abs/2502.16672