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Fluorescent RNA cytosine analogue – an internal probe for detailed structure and dynamics investigations

The bright fluorescent cytosine analogue tC(O) stands out among fluorescent bases due to its virtually unquenched fluorescence emission in duplex DNA. However, like most reported base analogues, it has not been thoroughly characterized in RNA. We here report on the first synthesis and RNA-incorporat...

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Autores principales: Füchtbauer, Anders Foller, Preus, Søren, Börjesson, Karl, McPhee, Scott A., Lilley, David M. J., Wilhelmsson, L. Marcus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5443824/
https://www.ncbi.nlm.nih.gov/pubmed/28539582
http://dx.doi.org/10.1038/s41598-017-02453-1
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author Füchtbauer, Anders Foller
Preus, Søren
Börjesson, Karl
McPhee, Scott A.
Lilley, David M. J.
Wilhelmsson, L. Marcus
author_facet Füchtbauer, Anders Foller
Preus, Søren
Börjesson, Karl
McPhee, Scott A.
Lilley, David M. J.
Wilhelmsson, L. Marcus
author_sort Füchtbauer, Anders Foller
collection PubMed
description The bright fluorescent cytosine analogue tC(O) stands out among fluorescent bases due to its virtually unquenched fluorescence emission in duplex DNA. However, like most reported base analogues, it has not been thoroughly characterized in RNA. We here report on the first synthesis and RNA-incorporation of tC(O), and characterize its base-mimicking and fluorescence properties in RNA. As in DNA, we find a high quantum yield inside RNA duplexes (<Φ(F)> = 0.22) that is virtually unaffected by the neighbouring bases (Φ(F) = 0.20–0.25), resulting in an average brightness of 1900 M(−1) cm(−1). The average fluorescence lifetime in RNA duplexes is 4.3 ns and generally two lifetimes are required to fit the exponential decays. Fluorescence properties in ssRNA are defined by a small increase in average quantum yield (<Φ(F )> = 0.24) compared to dsRNA, with a broader distribution (Φ(F) = 0.17–0.34) and slightly shorter average lifetimes. Using circular dichroism, we find that the tC(O)-modified RNA duplexes form regular A-form helices and in UV-melting experiments the stability of the duplexes is only slightly higher than that of the corresponding natural RNA (<ΔT (m)> = + 2.3 °C). These properties make tC(O) a highly interesting fluorescent RNA base analogue for detailed FRET-based structural measurements, as a bright internal label in microscopy, and for fluorescence anisotropy measurements of RNA dynamics.
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spelling pubmed-54438242017-05-26 Fluorescent RNA cytosine analogue – an internal probe for detailed structure and dynamics investigations Füchtbauer, Anders Foller Preus, Søren Börjesson, Karl McPhee, Scott A. Lilley, David M. J. Wilhelmsson, L. Marcus Sci Rep Article The bright fluorescent cytosine analogue tC(O) stands out among fluorescent bases due to its virtually unquenched fluorescence emission in duplex DNA. However, like most reported base analogues, it has not been thoroughly characterized in RNA. We here report on the first synthesis and RNA-incorporation of tC(O), and characterize its base-mimicking and fluorescence properties in RNA. As in DNA, we find a high quantum yield inside RNA duplexes (<Φ(F)> = 0.22) that is virtually unaffected by the neighbouring bases (Φ(F) = 0.20–0.25), resulting in an average brightness of 1900 M(−1) cm(−1). The average fluorescence lifetime in RNA duplexes is 4.3 ns and generally two lifetimes are required to fit the exponential decays. Fluorescence properties in ssRNA are defined by a small increase in average quantum yield (<Φ(F )> = 0.24) compared to dsRNA, with a broader distribution (Φ(F) = 0.17–0.34) and slightly shorter average lifetimes. Using circular dichroism, we find that the tC(O)-modified RNA duplexes form regular A-form helices and in UV-melting experiments the stability of the duplexes is only slightly higher than that of the corresponding natural RNA (<ΔT (m)> = + 2.3 °C). These properties make tC(O) a highly interesting fluorescent RNA base analogue for detailed FRET-based structural measurements, as a bright internal label in microscopy, and for fluorescence anisotropy measurements of RNA dynamics. Nature Publishing Group UK 2017-05-24 /pmc/articles/PMC5443824/ /pubmed/28539582 http://dx.doi.org/10.1038/s41598-017-02453-1 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Füchtbauer, Anders Foller
Preus, Søren
Börjesson, Karl
McPhee, Scott A.
Lilley, David M. J.
Wilhelmsson, L. Marcus
Fluorescent RNA cytosine analogue – an internal probe for detailed structure and dynamics investigations
title Fluorescent RNA cytosine analogue – an internal probe for detailed structure and dynamics investigations
title_full Fluorescent RNA cytosine analogue – an internal probe for detailed structure and dynamics investigations
title_fullStr Fluorescent RNA cytosine analogue – an internal probe for detailed structure and dynamics investigations
title_full_unstemmed Fluorescent RNA cytosine analogue – an internal probe for detailed structure and dynamics investigations
title_short Fluorescent RNA cytosine analogue – an internal probe for detailed structure and dynamics investigations
title_sort fluorescent rna cytosine analogue – an internal probe for detailed structure and dynamics investigations
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5443824/
https://www.ncbi.nlm.nih.gov/pubmed/28539582
http://dx.doi.org/10.1038/s41598-017-02453-1
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