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2′-O-Trifluoromethylated RNA – a powerful modification for RNA chemistry and NMR spectroscopy
New RNA modifications are needed to advance our toolbox for targeted manipulation of RNA. In particular, the development of high-performance reporter groups facilitating spectroscopic analysis of RNA structure and dynamics, and of RNA–ligand interactions has attracted considerable interest. To this...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8162808/ https://www.ncbi.nlm.nih.gov/pubmed/34094374 http://dx.doi.org/10.1039/d0sc04520a |
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author | Himmelstoß, Maximilian Erharter, Kevin Renard, Eva Ennifar, Eric Kreutz, Christoph Micura, Ronald |
author_facet | Himmelstoß, Maximilian Erharter, Kevin Renard, Eva Ennifar, Eric Kreutz, Christoph Micura, Ronald |
author_sort | Himmelstoß, Maximilian |
collection | PubMed |
description | New RNA modifications are needed to advance our toolbox for targeted manipulation of RNA. In particular, the development of high-performance reporter groups facilitating spectroscopic analysis of RNA structure and dynamics, and of RNA–ligand interactions has attracted considerable interest. To this end, fluorine labeling in conjunction with (19)F-NMR spectroscopy has emerged as a powerful strategy. Appropriate probes for RNA previously focused on single fluorine atoms attached to the 5-position of pyrimidine nucleobases or at the ribose 2′-position. To increase NMR sensitivity, trifluoromethyl labeling approaches have been developed, with the ribose 2′-SCF(3) modification being the most prominent one. A major drawback of the 2′-SCF(3) group, however, is its strong impact on RNA base pairing stability. Interestingly, RNA containing the structurally related 2′-OCF(3) modification has not yet been reported. Therefore, we set out to overcome the synthetic challenges toward 2′-OCF(3) labeled RNA and to investigate the impact of this modification. We present the syntheses of 2′-OCF(3) adenosine and cytidine phosphoramidites and their incorporation into oligoribonucleotides by solid-phase synthesis. Importantly, it turns out that the 2′-OCF(3) group has only a slight destabilizing effect when located in double helical regions which is consistent with the preferential C3′-endo conformation of the 2′-OCF(3) ribose as reflected in the (3)J (H1′–H2′) coupling constants. Furthermore, we demonstrate the exceptionally high sensitivity of the new label in (19)F-NMR analysis of RNA structure equilibria and of RNA–small molecule interactions. The study is complemented by a crystal structure at 0.9 Å resolution of a 27 nt hairpin RNA containing a single 2′-OCF(3) group that well integrates into the minor groove. The new label carries high potential to outcompete currently applied fluorine labels for nucleic acid NMR spectroscopy because of its significantly advanced performance. |
format | Online Article Text |
id | pubmed-8162808 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-81628082021-06-04 2′-O-Trifluoromethylated RNA – a powerful modification for RNA chemistry and NMR spectroscopy Himmelstoß, Maximilian Erharter, Kevin Renard, Eva Ennifar, Eric Kreutz, Christoph Micura, Ronald Chem Sci Chemistry New RNA modifications are needed to advance our toolbox for targeted manipulation of RNA. In particular, the development of high-performance reporter groups facilitating spectroscopic analysis of RNA structure and dynamics, and of RNA–ligand interactions has attracted considerable interest. To this end, fluorine labeling in conjunction with (19)F-NMR spectroscopy has emerged as a powerful strategy. Appropriate probes for RNA previously focused on single fluorine atoms attached to the 5-position of pyrimidine nucleobases or at the ribose 2′-position. To increase NMR sensitivity, trifluoromethyl labeling approaches have been developed, with the ribose 2′-SCF(3) modification being the most prominent one. A major drawback of the 2′-SCF(3) group, however, is its strong impact on RNA base pairing stability. Interestingly, RNA containing the structurally related 2′-OCF(3) modification has not yet been reported. Therefore, we set out to overcome the synthetic challenges toward 2′-OCF(3) labeled RNA and to investigate the impact of this modification. We present the syntheses of 2′-OCF(3) adenosine and cytidine phosphoramidites and their incorporation into oligoribonucleotides by solid-phase synthesis. Importantly, it turns out that the 2′-OCF(3) group has only a slight destabilizing effect when located in double helical regions which is consistent with the preferential C3′-endo conformation of the 2′-OCF(3) ribose as reflected in the (3)J (H1′–H2′) coupling constants. Furthermore, we demonstrate the exceptionally high sensitivity of the new label in (19)F-NMR analysis of RNA structure equilibria and of RNA–small molecule interactions. The study is complemented by a crystal structure at 0.9 Å resolution of a 27 nt hairpin RNA containing a single 2′-OCF(3) group that well integrates into the minor groove. The new label carries high potential to outcompete currently applied fluorine labels for nucleic acid NMR spectroscopy because of its significantly advanced performance. The Royal Society of Chemistry 2020-09-24 /pmc/articles/PMC8162808/ /pubmed/34094374 http://dx.doi.org/10.1039/d0sc04520a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Himmelstoß, Maximilian Erharter, Kevin Renard, Eva Ennifar, Eric Kreutz, Christoph Micura, Ronald 2′-O-Trifluoromethylated RNA – a powerful modification for RNA chemistry and NMR spectroscopy |
title | 2′-O-Trifluoromethylated RNA – a powerful modification for RNA chemistry and NMR spectroscopy |
title_full | 2′-O-Trifluoromethylated RNA – a powerful modification for RNA chemistry and NMR spectroscopy |
title_fullStr | 2′-O-Trifluoromethylated RNA – a powerful modification for RNA chemistry and NMR spectroscopy |
title_full_unstemmed | 2′-O-Trifluoromethylated RNA – a powerful modification for RNA chemistry and NMR spectroscopy |
title_short | 2′-O-Trifluoromethylated RNA – a powerful modification for RNA chemistry and NMR spectroscopy |
title_sort | 2′-o-trifluoromethylated rna – a powerful modification for rna chemistry and nmr spectroscopy |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8162808/ https://www.ncbi.nlm.nih.gov/pubmed/34094374 http://dx.doi.org/10.1039/d0sc04520a |
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