Reversible chemical reactions for single-color multiplexing microscopy

Abstract Recent developments in biology demand an increasing number of simultaneously imaged structures with standard fluorescence microscopy. However, the number of multiplexed channels is limited for most multiplexing modalities, such as spectral multiplexing or fluorescence-lifetime imaging. We p...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Brox, Dominik (VerfasserIn) , Schwering, Michael (VerfasserIn) , Engelhardt, Johann (VerfasserIn) , Herten, Dirk-Peter (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 17 April 2014
In: ChemPhysChem
Year: 2014, Jahrgang: 15, Heft: 11, Pages: 2331-2336
ISSN:1439-7641
DOI:10.1002/cphc.201402012
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1002/cphc.201402012
Verlag, lizenzpflichtig, Volltext: https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/cphc.201402012
Volltext
Verfasserangaben:Dominik Brox, Michael Schwering, Johann Engelhardt, Dirk-Peter Herten
Beschreibung
Zusammenfassung:Abstract Recent developments in biology demand an increasing number of simultaneously imaged structures with standard fluorescence microscopy. However, the number of multiplexed channels is limited for most multiplexing modalities, such as spectral multiplexing or fluorescence-lifetime imaging. We propose extending the number of imaging channels by using chemical reactions, controlling the emissive state of fluorescent dyes. As proof of concept, we reversibly switch a fluorescent copper sensor to enable successive imaging of two different structures in the same spectral channel. We also show that this chemical multiplexing is orthogonal to existing methods. By using two different dyes, we combine chemical with spectral multiplexing for the simultaneous imaging of four different structures with only two spectrally different channels. We characterize and discuss the approach and provide perspectives for extending imaging modalities in stimulated emission depletion microscopy, for which spectral multiplexing is technically demanding.
Beschreibung:Gesehen am 27.08.2020
Beschreibung:Online Resource
ISSN:1439-7641
DOI:10.1002/cphc.201402012