Issue 41, 2020

2′-O-Trifluoromethylated RNA – a powerful modification for RNA chemistry and NMR spectroscopy

Abstract

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 19F-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′-SCF3 modification being the most prominent one. A major drawback of the 2′-SCF3 group, however, is its strong impact on RNA base pairing stability. Interestingly, RNA containing the structurally related 2′-OCF3 modification has not yet been reported. Therefore, we set out to overcome the synthetic challenges toward 2′-OCF3 labeled RNA and to investigate the impact of this modification. We present the syntheses of 2′-OCF3 adenosine and cytidine phosphoramidites and their incorporation into oligoribonucleotides by solid-phase synthesis. Importantly, it turns out that the 2′-OCF3 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′-OCF3 ribose as reflected in the 3J (H1′–H2′) coupling constants. Furthermore, we demonstrate the exceptionally high sensitivity of the new label in 19F-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′-OCF3 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.

Graphical abstract: 2′-O-Trifluoromethylated RNA – a powerful modification for RNA chemistry and NMR spectroscopy

Supplementary files

Article information

Article type
Edge Article
Submitted
18 Aug 2020
Accepted
18 Sep 2020
First published
24 Sep 2020
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2020,11, 11322-11330

2′-O-Trifluoromethylated RNA – a powerful modification for RNA chemistry and NMR spectroscopy

M. Himmelstoß, K. Erharter, E. Renard, E. Ennifar, C. Kreutz and R. Micura, Chem. Sci., 2020, 11, 11322 DOI: 10.1039/D0SC04520A

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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