| Literature DB >> 35792810 |
Nazar Oleksiievets1, Christeena Mathew2, Jan Christoph Thiele1, José Ignacio Gallea1, Oleksii Nevskyi1, Ingo Gregor1, André Weber3, Roman Tsukanov1, Jörg Enderlein1,4.
Abstract
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.Entities:
Keywords: DNA-PAINT; fluorescence lifetime; fluorescence lifetime imaging microscopy; metal-induced energy transfer; single-molecule localization microscopy; super-resolution microscopy
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Year: 2022 PMID: 35792810 PMCID: PMC9373986 DOI: 10.1021/acs.nanolett.2c01586
Source DB: PubMed Journal: Nano Lett ISSN: 1530-6984 Impact factor: 12.262