MINFLUX fluorescence nanoscopy in biological tissue

Optical imaging access to nanometer-level protein distributions in intact tissue is a highly sought-after goal, as it would provide visualization in physiologically relevant contexts. Under the unfavorable signal-to-background conditions of increased absorption and scattering of the excitation and f...

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Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS 2024-12, Vol.121 (52), p.e2422020121
Hauptverfasser: Moosmayer, Thea, Kiszka, Kamila A, Westphal, Volker, Pape, Jasmin K, Leutenegger, Marcel, Steffens, Heinz, Grant, Seth G N, Sahl, Steffen J, Hell, Stefan W
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Sprache:eng
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Zusammenfassung:Optical imaging access to nanometer-level protein distributions in intact tissue is a highly sought-after goal, as it would provide visualization in physiologically relevant contexts. Under the unfavorable signal-to-background conditions of increased absorption and scattering of the excitation and fluorescence light in the complex tissue sample, superresolution fluorescence microscopy methods are severely challenged in attaining precise localization of molecules. We reasoned that the typical use of a confocal detection pinhole in MINFLUX nanoscopy, suppressing background and providing optical sectioning, should facilitate the detection and resolution of single fluorophores even amid scattering and optically challenging tissue environments. Here, we investigated the performance of MINFLUX imaging for different synaptic targets and fluorescent labels in tissue sections of the mouse brain. Single fluorophores were localized with a precision of
ISSN:0027-8424
1091-6490
1091-6490
DOI:10.1073/pnas.2422020121