Cargando…
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...
Autores principales: | , , , , , , , , |
---|---|
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 |
_version_ | 1784767699773030400 |
---|---|
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. |
format | Online Article Text |
id | pubmed-9373986 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT oleksiievetsnazar singlemoleculefluorescencelifetimeimagingusingwidefieldandconfocallaserscanningmicroscopyacomparativeanalysis AT mathewchristeena singlemoleculefluorescencelifetimeimagingusingwidefieldandconfocallaserscanningmicroscopyacomparativeanalysis AT thielejanchristoph singlemoleculefluorescencelifetimeimagingusingwidefieldandconfocallaserscanningmicroscopyacomparativeanalysis AT galleajoseignacio singlemoleculefluorescencelifetimeimagingusingwidefieldandconfocallaserscanningmicroscopyacomparativeanalysis AT nevskyioleksii singlemoleculefluorescencelifetimeimagingusingwidefieldandconfocallaserscanningmicroscopyacomparativeanalysis AT gregoringo singlemoleculefluorescencelifetimeimagingusingwidefieldandconfocallaserscanningmicroscopyacomparativeanalysis AT weberandre singlemoleculefluorescencelifetimeimagingusingwidefieldandconfocallaserscanningmicroscopyacomparativeanalysis AT tsukanovroman singlemoleculefluorescencelifetimeimagingusingwidefieldandconfocallaserscanningmicroscopyacomparativeanalysis AT enderleinjorg singlemoleculefluorescencelifetimeimagingusingwidefieldandconfocallaserscanningmicroscopyacomparativeanalysis |