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Amphiphilic coumarin-based probes for live-cell STED nanoscopy of plasma membrane.
Kokot, Hana; Kokot, Bostjan; Pislar, Anja; Esih, Hana; Gabric, Alen; Urbancic, Dunja; El, Rojbin; Urbancic, Iztok; Pajk, Stane.
Afiliação
  • Kokot H; Jozef Stefan Institute, Jamova cesta 39, SI-1000 Ljubljana, Slovenia.
  • Kokot B; Jozef Stefan Institute, Jamova cesta 39, SI-1000 Ljubljana, Slovenia.
  • Pislar A; University of Ljubljana, Faculty of Pharmacy, SI-1000 Ljubljana, Slovenia.
  • Esih H; University of Ljubljana, Faculty of Pharmacy, SI-1000 Ljubljana, Slovenia.
  • Gabric A; University of Ljubljana, Faculty of Pharmacy, SI-1000 Ljubljana, Slovenia.
  • Urbancic D; University of Ljubljana, Faculty of Pharmacy, SI-1000 Ljubljana, Slovenia; Weatherall Institute of Molecular Medicine, University of Oxford, OX3 9DS Oxford, United Kingdom.
  • El R; Weatherall Institute of Molecular Medicine, University of Oxford, OX3 9DS Oxford, United Kingdom.
  • Urbancic I; Jozef Stefan Institute, Jamova cesta 39, SI-1000 Ljubljana, Slovenia; Weatherall Institute of Molecular Medicine, University of Oxford, OX3 9DS Oxford, United Kingdom.
  • Pajk S; University of Ljubljana, Faculty of Pharmacy, SI-1000 Ljubljana, Slovenia. Electronic address: stane.pajk@ffa.uni-lj.si.
Bioorg Chem ; 150: 107554, 2024 Sep.
Article em En | MEDLINE | ID: mdl-38878753
ABSTRACT
Plasma membranes are vital biological structures, serving as protective barriers and participating in various cellular processes. In the field of super-resolution optical microscopy, stimulated emission depletion (STED) nanoscopy has emerged as a powerful method for investigating plasma membrane-related phenomena. However, many applications of STED microscopy are critically restricted by the limited availability of suitable fluorescent probes. This paper reports on the development of two amphiphilic membrane probes, SHE-2H and SHE-2N, specially designed for STED nanoscopy. SHE-2N, in particular, demonstrates quick and stable plasma membrane labelling with negligible intracellular redistribution. Both probes exhibit outstanding photostability and resolution improvement in STED nanoscopy, and are also suited for two-photon excitation microscopy. Furthermore, microscopy experiments and cytotoxicity tests revealed no noticeable cytotoxicity of probe SHE-2N at concentration used for fluorescence imaging. Spectral analysis and fluorescence lifetime measurements conducted on probe SHE-2N using giant unilamellar vesicles, revealed that emission spectra and fluorescence lifetimes exhibited minimal sensitivity to lipid composition variations. These novel probes significantly augment the arsenal of tools available for high-resolution plasma membrane research, enabling a more profound exploration of cellular processes and dynamics.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article