| Literature DB >> 26237536 |
Sandro Neuner1, Tobias Santner1, Christoph Kreutz1, Ronald Micura1.
Abstract
Although numerous reports on the synthesis of atom-specific (15)N-labeled nucleosides exist, fast and facile access to the corresponding phosphoramidites for RNA solid-phase synthesis is still lacking. This situation represents a severe bottleneck for NMR spectroscopic investigations on functional RNAs. Here, we present optimized procedures to speed up the synthesis of (15)N(1) adenosine and (15)N(1) guanosine amidites, which are the much needed counterparts of the more straightforward-to-achieve (15)N(3) uridine and (15)N(3) cytidine amidites in order to tap full potential of (1)H/(15)N/(15)N-COSY experiments for directly monitoring individual Watson-Crick base pairs in RNA. Demonstrated for two preQ1 riboswitch systems, we exemplify a versatile concept for individual base-pair labeling in the analysis of conformationally flexible RNAs when competing structures and conformational dynamics are encountered.Entities:
Keywords: NMR spectroscopy; nucleosides; oligonucleotides; phosphoramidites
Mesh:
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Year: 2015 PMID: 26237536 PMCID: PMC4946632 DOI: 10.1002/chem.201501275
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236