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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...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2018
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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 |
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author | 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 |
author_facet | 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 |
author_sort | Bood, Mattias |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-5934695 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-59346952018-05-18 Pentacyclic adenine: a versatile and exceptionally bright fluorescent DNA base analogue 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 Chem Sci Chemistry 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. Royal Society of Chemistry 2018-03-01 /pmc/articles/PMC5934695/ /pubmed/29780479 http://dx.doi.org/10.1039/c7sc05448c Text en This journal is © The Royal Society of Chemistry 2018 http://creativecommons.org/licenses/by/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0) |
spellingShingle | Chemistry 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 Pentacyclic adenine: a versatile and exceptionally bright fluorescent DNA base analogue |
title | Pentacyclic adenine: a versatile and exceptionally bright fluorescent DNA base analogue
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title_full | Pentacyclic adenine: a versatile and exceptionally bright fluorescent DNA base analogue
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title_fullStr | Pentacyclic adenine: a versatile and exceptionally bright fluorescent DNA base analogue
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title_full_unstemmed | Pentacyclic adenine: a versatile and exceptionally bright fluorescent DNA base analogue
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title_short | Pentacyclic adenine: a versatile and exceptionally bright fluorescent DNA base analogue
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title_sort | pentacyclic adenine: a versatile and exceptionally bright fluorescent dna base analogue |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5934695/ https://www.ncbi.nlm.nih.gov/pubmed/29780479 http://dx.doi.org/10.1039/c7sc05448c |
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