Single-Molecule Fluorescence Lifetime Imaging Using Wide-Field and Confocal-Laser Scanning Microscopy: A Comparative Analysis
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...
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Veröffentlicht in: | Nano letters 2022-08, Vol.22 (15), p.6454-6461 |
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creator | Oleksiievets, Nazar Mathew, Christeena Thiele, Jan Christoph Gallea, José Ignacio Nevskyi, Oleksii Gregor, Ingo Weber, André Tsukanov, Roman Enderlein, Jörg |
description | 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. |
doi_str_mv | 10.1021/acs.nanolett.2c01586 |
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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.</description><identifier>ISSN: 1530-6984</identifier><identifier>ISSN: 1530-6992</identifier><identifier>EISSN: 1530-6992</identifier><identifier>DOI: 10.1021/acs.nanolett.2c01586</identifier><identifier>PMID: 35792810</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>DNA ; Letter ; Microscopy, Confocal - methods ; Microscopy, Fluorescence - methods ; Nanotechnology ; Single Molecule Imaging - methods</subject><ispartof>Nano letters, 2022-08, Vol.22 (15), p.6454-6461</ispartof><rights>2022 The Authors. Published by American Chemical Society</rights><rights>2022 The Authors. 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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.</description><subject>DNA</subject><subject>Letter</subject><subject>Microscopy, Confocal - methods</subject><subject>Microscopy, Fluorescence - methods</subject><subject>Nanotechnology</subject><subject>Single Molecule Imaging - methods</subject><issn>1530-6984</issn><issn>1530-6992</issn><issn>1530-6992</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU9v2yAYxtG0af23bzBNPu7iDAzYZodJUbS0lVLt0FY7IgyvMyoMGdiVcth3L1bSaLvsAkj8ngee90HoI8ELgivyRem08MoHB-O4qDQmvK3foHPCKS5rIaq3p3PLztBFSk8YY0E5fo_OKG9E1RJ8jv7cW791UN5lHz05KNZuChGSBq-h2NgeRjtAcTuobQaLxzSvP62Bcm3BmUJ5U6yC74NWrtyoBLG418r7GbuzOoakw27_tVhmatipqEb7DMXSK7dPNl2hd71yCT4c90v0uP7-sLopNz-ub1fLTakYE2NJSa14p6umMmCg55xB3WDTNYwx0hoMPOcltDJtJzCtoROC951oCK55X7eaXqJvB9_d1A1gcrgxKid30Q4q7mVQVv574-0vuQ3PUtCGirbOBp-PBjH8niCNcrB5Rs4pD2FKsqpbzhhvBc0oO6Bz-BShPz1DsJybk7k5-dqcPDaXZZ_-_uJJ9FpVBvABmOVPYYp5hun_ni-DXasb</recordid><startdate>20220810</startdate><enddate>20220810</enddate><creator>Oleksiievets, Nazar</creator><creator>Mathew, Christeena</creator><creator>Thiele, Jan Christoph</creator><creator>Gallea, José Ignacio</creator><creator>Nevskyi, Oleksii</creator><creator>Gregor, Ingo</creator><creator>Weber, André</creator><creator>Tsukanov, Roman</creator><creator>Enderlein, Jörg</creator><general>American Chemical Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-2893-481X</orcidid><orcidid>https://orcid.org/0000-0002-1775-2159</orcidid><orcidid>https://orcid.org/0000-0002-6638-6298</orcidid><orcidid>https://orcid.org/0000-0001-5091-7157</orcidid><orcidid>https://orcid.org/0000-0001-7752-2112</orcidid><orcidid>https://orcid.org/0000-0002-3967-1755</orcidid></search><sort><creationdate>20220810</creationdate><title>Single-Molecule Fluorescence Lifetime Imaging Using Wide-Field and Confocal-Laser Scanning Microscopy: A Comparative Analysis</title><author>Oleksiievets, Nazar ; Mathew, Christeena ; Thiele, Jan Christoph ; Gallea, José Ignacio ; Nevskyi, Oleksii ; Gregor, Ingo ; Weber, André ; Tsukanov, Roman ; Enderlein, Jörg</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a449t-316a5bc272dedef554e670db744418d0e5992132d8b9036eb995fb971065f68c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>DNA</topic><topic>Letter</topic><topic>Microscopy, Confocal - methods</topic><topic>Microscopy, Fluorescence - methods</topic><topic>Nanotechnology</topic><topic>Single Molecule Imaging - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Oleksiievets, Nazar</creatorcontrib><creatorcontrib>Mathew, Christeena</creatorcontrib><creatorcontrib>Thiele, Jan Christoph</creatorcontrib><creatorcontrib>Gallea, José Ignacio</creatorcontrib><creatorcontrib>Nevskyi, Oleksii</creatorcontrib><creatorcontrib>Gregor, Ingo</creatorcontrib><creatorcontrib>Weber, André</creatorcontrib><creatorcontrib>Tsukanov, Roman</creatorcontrib><creatorcontrib>Enderlein, Jörg</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Nano letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Oleksiievets, Nazar</au><au>Mathew, Christeena</au><au>Thiele, Jan Christoph</au><au>Gallea, José Ignacio</au><au>Nevskyi, Oleksii</au><au>Gregor, Ingo</au><au>Weber, André</au><au>Tsukanov, Roman</au><au>Enderlein, Jörg</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Single-Molecule Fluorescence Lifetime Imaging Using Wide-Field and Confocal-Laser Scanning Microscopy: A Comparative Analysis</atitle><jtitle>Nano letters</jtitle><addtitle>Nano Lett</addtitle><date>2022-08-10</date><risdate>2022</risdate><volume>22</volume><issue>15</issue><spage>6454</spage><epage>6461</epage><pages>6454-6461</pages><issn>1530-6984</issn><issn>1530-6992</issn><eissn>1530-6992</eissn><abstract>A recent addition to the toolbox of super-resolution microscopy methods is fluorescence-lifetime single-molecule localization microscopy (FL-SMLM). 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subjects | DNA Letter Microscopy, Confocal - methods Microscopy, Fluorescence - methods Nanotechnology Single Molecule Imaging - methods |
title | Single-Molecule Fluorescence Lifetime Imaging Using Wide-Field and Confocal-Laser Scanning Microscopy: A Comparative Analysis |
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