Real-time Imaging of Nascent DNA in Live Cells by Monitoring the Fluorescence Lifetime of DNA-Incorporated Thiazole Orange-Modified Nucleotides
Jazyk angličtina Země Německo Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
37498132
DOI
10.1002/anie.202307548
Knihovny.cz E-zdroje
- Klíčová slova
- DNA Synthesis, Fluorescence Lifetime Imaging Microscopy, Fluorophores, Metabolic Labelling, Nucleotides,
- MeSH
- benzothiazoly MeSH
- DNA * metabolismus MeSH
- fluorescence MeSH
- nukleotidy * MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- benzothiazoly MeSH
- DNA * MeSH
- nukleotidy * MeSH
- thiazole orange MeSH Prohlížeč
A modified 2'-deoxycytidine triphosphate derivative (dCTO TP) bearing a thiazole orange moiety tethered via an oligoethylene glycol linker was designed and synthesized. The nucleotide was incorporated into DNA by DNA polymerases in vitro as well as in live cells. Upon incorporation of dCTO TP into DNA, the thiazole orange moiety exhibited a fluorescence lifetime that differed significantly from the non-incorporated (i.e. free and non-covalently intercalated) forms of dCTO TP. When dCTO TP was delivered into live U-2 OS cells using a synthetic nucleoside triphosphate transporter, it allowed us to distinguish and monitor cells that were actively synthesizing DNA in real time, from the very first moments after the treatment. We anticipate that this probe could be used to study chromatin organization and dynamics.
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