| Literature DB >> 33095954 |
Michael Weber1, Taukeer A Khan1, Lukas J Patalag1,2, Mariano Bossi3, Marcel Leutenegger1, Vladimir N Belov1, Stefan W Hell1,3.
Abstract
The use of photoactivatable dyes in STED microscopy has so far been limited by two-photon activation through the STED beam and by the fact that photoactivatable dyes are poorly solvable in water. Herein, we report ONB-2SiR, a fluorophore that can be both photoactivated in the UV and specifically de-excited by STED at 775 nm. Likewise, we introduce a conjugation and purification protocol to effectively label primary and secondary antibodies with moderately water-soluble dyes. Greatly reducing dye aggregation, our technique provides a defined and tunable degree of labeling, and improves the imaging performance of dye conjugates in general.Entities:
Keywords: fluorescence; optical superresolution; photoactivation; protein labelling; stimulated emission depletion (STED)
Mesh:
Substances:
Year: 2020 PMID: 33095954 PMCID: PMC7839434 DOI: 10.1002/chem.202004645
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236