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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.
Affiliation
  • Oleksiievets N; III. Institute of Physics - Biophysics, Georg August University, 37077 Göttingen, Germany.
  • Mathew C; Laboratory of Supramolecular Chemistry, EPFL SB ISIC LCS, BCH 3307, CH-1015 Lausanne, Switzerland.
  • Thiele JC; III. Institute of Physics - Biophysics, Georg August University, 37077 Göttingen, Germany.
  • Gallea JI; III. Institute of Physics - Biophysics, Georg August University, 37077 Göttingen, Germany.
  • Nevskyi O; III. Institute of Physics - Biophysics, Georg August University, 37077 Göttingen, Germany.
  • Gregor I; III. Institute of Physics - Biophysics, Georg August University, 37077 Göttingen, Germany.
  • Weber A; Combinatorial NeuroImaging Core Facility, Leibniz Institute for Neurobiology, Brenneckestraße 6, 39118 Magdeburg, Germany.
  • Tsukanov R; III. Institute of Physics - Biophysics, Georg August University, 37077 Göttingen, Germany.
  • Enderlein J; III. Institute of Physics - Biophysics, Georg August University, 37077 Göttingen, Germany.
Nano Lett ; 22(15): 6454-6461, 2022 08 10.
Article in En | MEDLINE | ID: mdl-35792810
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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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA / Single Molecule Imaging Language: En Journal: Nano Lett Year: 2022 Document type: Article Affiliation country: Germany Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA / Single Molecule Imaging Language: En Journal: Nano Lett Year: 2022 Document type: Article Affiliation country: Germany Country of publication: United States