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Synthesis and application of a 19F-labeled fluorescent nucleoside as a dual-mode probe for i-motif DNAs.


ABSTRACT: Because of their stable orientations and their minimal interference with native DNA interactions and folding, emissive isomorphic nucleoside analogues are versatile tools for the accurate analysis of DNA structural heterogeneity. Here, we report on a bifunctional trifluoromethylphenylpyrrolocytidine derivative (FPdC) that displays an unprecedented quantum yield and highly sensitive 19F NMR signal. This is the first report of a cytosine-based dual-purpose probe for both fluorescence and 19F NMR spectroscopic DNA analysis. FPdC and FPdC-containing DNA were synthesized and characterized; our robust dual probe was successfully used to investigate the noncanonical DNA structure, i-motifs, through changes in fluorescence intensity and 19F chemical shift in response to i-motif formation. The utility of FPdC was exemplified through reversible fluorescence switching of an FPdC-containing i-motif oligonucleotide in the presence of Ag(i) and cysteine.

SUBMITTER: Wee WA 

PROVIDER: S-EPMC8382138 | biostudies-literature | 2021 Jun

REPOSITORIES: biostudies-literature

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Synthesis and application of a <sup>19</sup>F-labeled fluorescent nucleoside as a dual-mode probe for i-motif DNAs.

Wee Wen Ann WA   Yum Ji Hye JH   Hirashima Shingo S   Sugiyama Hiroshi H   Park Soyoung S  

RSC chemical biology 20210310 3


Because of their stable orientations and their minimal interference with native DNA interactions and folding, emissive isomorphic nucleoside analogues are versatile tools for the accurate analysis of DNA structural heterogeneity. Here, we report on a bifunctional trifluoromethylphenylpyrrolocytidine derivative (<b>FPdC</b>) that displays an unprecedented quantum yield and highly sensitive <sup>19</sup>F NMR signal. This is the first report of a cytosine-based dual-purpose probe for both fluoresc  ...[more]

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