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Pentacyclic adenine: a versatile and exceptionally bright fluorescent DNA base analogue

Emissive base analogs are powerful tools for probing nucleic acids at the molecular level. Herein we describe the development and thorough characterization of pentacyclic adenine (pA), a versatile base analog with exceptional fluorescence properties. When incorporated into DNA, pA pairs selectively...

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Detalles Bibliográficos
Autores principales: Bood, Mattias, Füchtbauer, Anders F., Wranne, Moa S., Ro, Jong Jin, Sarangamath, Sangamesh, El-Sagheer, Afaf H., Rupert, Déborah L. M., Fisher, Rachel S., Magennis, Steven W., Jones, Anita C., Höök, Fredrik, Brown, Tom, Kim, Byeang Hyean, Dahlén, Anders, Wilhelmsson, L. Marcus, Grøtli, Morten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5934695/
https://www.ncbi.nlm.nih.gov/pubmed/29780479
http://dx.doi.org/10.1039/c7sc05448c
Descripción
Sumario:Emissive base analogs are powerful tools for probing nucleic acids at the molecular level. Herein we describe the development and thorough characterization of pentacyclic adenine (pA), a versatile base analog with exceptional fluorescence properties. When incorporated into DNA, pA pairs selectively with thymine without perturbing the B-form structure and is among the brightest nucleobase analogs reported so far. Together with the recently established base analog acceptor qA(nitro), pA allows accurate distance and orientation determination via Förster resonance energy transfer (FRET) measurements. The high brightness at emission wavelengths above 400 nm also makes it suitable for fluorescence microscopy, as demonstrated by imaging of single liposomal constructs coated with cholesterol-anchored pA–dsDNA, using total internal reflection fluorescence microscopy. Finally, pA is also highly promising for two-photon excitation at 780 nm, with a brightness (5.3 GM) that is unprecedented for a base analog.