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Single-Molecule Fluorescence Lifetime Imaging Using Wide-Field and Confocal-Laser Scanning Microscopy: A Comparative Analysis

[Image: see text] A recent addition to the toolbox of super-resolution microscopy methods is fluorescence-lifetime single-molecule localization microscopy (FL-SMLM). The synergy of SMLM and fluorescence-lifetime imaging microscopy (FLIM) combines superior image resolution with lifetime information a...

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Autores principales: Oleksiievets, Nazar, Mathew, Christeena, Thiele, Jan Christoph, Gallea, José Ignacio, Nevskyi, Oleksii, Gregor, Ingo, Weber, André, Tsukanov, Roman, Enderlein, Jörg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9373986/
https://www.ncbi.nlm.nih.gov/pubmed/35792810
http://dx.doi.org/10.1021/acs.nanolett.2c01586
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author Oleksiievets, Nazar
Mathew, Christeena
Thiele, Jan Christoph
Gallea, José Ignacio
Nevskyi, Oleksii
Gregor, Ingo
Weber, André
Tsukanov, Roman
Enderlein, Jörg
author_facet Oleksiievets, Nazar
Mathew, Christeena
Thiele, Jan Christoph
Gallea, José Ignacio
Nevskyi, Oleksii
Gregor, Ingo
Weber, André
Tsukanov, Roman
Enderlein, Jörg
author_sort Oleksiievets, Nazar
collection PubMed
description [Image: see text] A recent addition to the toolbox of super-resolution microscopy methods is fluorescence-lifetime single-molecule localization microscopy (FL-SMLM). The synergy of SMLM and fluorescence-lifetime imaging microscopy (FLIM) combines superior image resolution with lifetime information and can be realized using two complementary experimental approaches: confocal-laser scanning microscopy (CLSM) or wide-field microscopy. Here, we systematically and comprehensively compare these two novel FL-SMLM approaches in different spectral regions. For wide-field FL-SMLM, we use a commercial lifetime camera, and for CLSM-based FL-SMLM we employ a home-built system equipped with a rapid scan unit and a single-photon detector. We characterize the performances of the two systems in localizing single emitters in 3D by combining FL-SMLM with metal-induced energy transfer (MIET) for localization along the third dimension and in the lifetime-based multiplexed bioimaging using DNA-PAINT. Finally, we discuss advantages and disadvantages of wide-field and confocal FL-SMLM and provide practical advice on rational FL-SMLM experiment design.
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spelling pubmed-93739862023-07-06 Single-Molecule Fluorescence Lifetime Imaging Using Wide-Field and Confocal-Laser Scanning Microscopy: A Comparative Analysis Oleksiievets, Nazar Mathew, Christeena Thiele, Jan Christoph Gallea, José Ignacio Nevskyi, Oleksii Gregor, Ingo Weber, André Tsukanov, Roman Enderlein, Jörg Nano Lett [Image: see text] A recent addition to the toolbox of super-resolution microscopy methods is fluorescence-lifetime single-molecule localization microscopy (FL-SMLM). The synergy of SMLM and fluorescence-lifetime imaging microscopy (FLIM) combines superior image resolution with lifetime information and can be realized using two complementary experimental approaches: confocal-laser scanning microscopy (CLSM) or wide-field microscopy. Here, we systematically and comprehensively compare these two novel FL-SMLM approaches in different spectral regions. For wide-field FL-SMLM, we use a commercial lifetime camera, and for CLSM-based FL-SMLM we employ a home-built system equipped with a rapid scan unit and a single-photon detector. We characterize the performances of the two systems in localizing single emitters in 3D by combining FL-SMLM with metal-induced energy transfer (MIET) for localization along the third dimension and in the lifetime-based multiplexed bioimaging using DNA-PAINT. Finally, we discuss advantages and disadvantages of wide-field and confocal FL-SMLM and provide practical advice on rational FL-SMLM experiment design. American Chemical Society 2022-07-06 2022-08-10 /pmc/articles/PMC9373986/ /pubmed/35792810 http://dx.doi.org/10.1021/acs.nanolett.2c01586 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Oleksiievets, Nazar
Mathew, Christeena
Thiele, Jan Christoph
Gallea, José Ignacio
Nevskyi, Oleksii
Gregor, Ingo
Weber, André
Tsukanov, Roman
Enderlein, Jörg
Single-Molecule Fluorescence Lifetime Imaging Using Wide-Field and Confocal-Laser Scanning Microscopy: A Comparative Analysis
title Single-Molecule Fluorescence Lifetime Imaging Using Wide-Field and Confocal-Laser Scanning Microscopy: A Comparative Analysis
title_full Single-Molecule Fluorescence Lifetime Imaging Using Wide-Field and Confocal-Laser Scanning Microscopy: A Comparative Analysis
title_fullStr Single-Molecule Fluorescence Lifetime Imaging Using Wide-Field and Confocal-Laser Scanning Microscopy: A Comparative Analysis
title_full_unstemmed Single-Molecule Fluorescence Lifetime Imaging Using Wide-Field and Confocal-Laser Scanning Microscopy: A Comparative Analysis
title_short Single-Molecule Fluorescence Lifetime Imaging Using Wide-Field and Confocal-Laser Scanning Microscopy: A Comparative Analysis
title_sort single-molecule fluorescence lifetime imaging using wide-field and confocal-laser scanning microscopy: a comparative analysis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9373986/
https://www.ncbi.nlm.nih.gov/pubmed/35792810
http://dx.doi.org/10.1021/acs.nanolett.2c01586
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