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Amphiphilic coumarin-based probes for live-cell STED nanoscopy of plasma membrane
ID
Kokot, Hana
(
Author
),
ID
Kokot, Boštjan
(
Author
),
ID
Pišlar, Anja
(
Author
),
ID
Esih, Hana
(
Author
),
ID
Gabrič, Alen
(
Author
),
ID
Urbančič, Dunja
(
Author
),
ID
El, Rojbin
(
Author
),
ID
Urbančič, Iztok
(
Author
),
ID
Pajk, Stane
(
Author
)
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https://www.sciencedirect.com/science/article/pii/S0045206824004590
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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.
Language:
English
Keywords:
membrane probe
,
fluorescence
,
STED
,
two-photon excitation
,
photostability
Work type:
Article
Typology:
1.01 - Original Scientific Article
Organization:
FFA - Faculty of Pharmacy
Publication status:
Published
Publication version:
Version of Record
Year:
2024
Number of pages:
10 str.
Numbering:
Vol. 150, art. 107554
PID:
20.500.12556/RUL-158633
UDC:
539
ISSN on article:
0045-2068
DOI:
10.1016/j.bioorg.2024.107554
COBISS.SI-ID:
198949635
Publication date in RUL:
18.06.2024
Views:
292
Downloads:
68
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Record is a part of a journal
Title:
Bioorganic chemistry
Shortened title:
Bioorg. chem.
Publisher:
Elsevier
ISSN:
0045-2068
COBISS.SI-ID:
25099008
Licences
License:
CC BY-NC 4.0, Creative Commons Attribution-NonCommercial 4.0 International
Link:
http://creativecommons.org/licenses/by-nc/4.0/
Description:
A creative commons license that bans commercial use, but the users don’t have to license their derivative works on the same terms.
Secondary language
Language:
Slovenian
Keywords:
fizika
,
membrane
,
fluorescenca
Projects
Funder:
ARIS - Slovenian Research and Innovation Agency
Project number:
P1-0208
Name:
Farmacevtska kemija: načrtovanje, sinteza in vrednotenje učinkovin
Funder:
ARIS - Slovenian Research and Innovation Agency
Project number:
P1-0060
Name:
Eksperimentalna biofizika kompleksnih sistemov in slikanje v biomedicini
Funder:
ARIS - Slovenian Research and Innovation Agency
Project number:
J3-3079
Name:
Baktericidna nanorezila: preizkus bimodalnega mehanokemijskega odstranjevanja trdovratnih biofilmov
Funder:
ARIS - Slovenian Research and Innovation Agency
Project number:
J7-2596
Name:
Pametna nanospektroskopija molekularnih dogodkov pri nevrodegeneraciji zaradi nanodelcev
Funder:
ARIS - Slovenian Research and Innovation Agency
Project number:
N1-0240
Name:
Identifikacija ključnih dogodkov v živih celicah na podlagi mikroskopije
Funder:
Other - Other funder or multiple funders
Funding programme:
Slovenia, Ministry of Higher Education, Science and Innovation
Funder:
EC - European Commission
Funding programme:
European Regional Development Fund
Project number:
OP20.05187
Acronym:
RI-SI-EATRIS
Funder:
EC - European Commission
Funding programme:
H2020
Project number:
707348
Name:
Development of fluorescence nanospectroscopy to elucidate the roles of nanoscale molecular segregation in the activation of T-cells
Acronym:
FNS-4-NAMOSAT
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