Phenoxazine pseudonucleotides in DNA i-motifs allow precise profiling of small molecule binders by fluorescence monitoring

The lack of high throughput screening (HTS) techniques for small molecules that stabilize DNA iMs limits their development as perspective drug candidates. Here we showed that fluorescence monitoring for probing the effects of ligands on the iM stability using the FAM-BHQ1 pair provides incorrect res...

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Published inAnalyst (London) Vol. 146; no. 14; pp. 4436 - 444
Main Authors Tsvetkov, Vladimir B, Turaev, Anton V, Petrunina, Nataliia A, Melnik, Denis M, Khodarovich, Yuriy M, Pozmogova, Galina E, Zatsepin, Timofei S, Varizhuk, Anna M, Aralov, Andrey V
Format Journal Article
LanguageEnglish
Published London Royal Society of Chemistry 21.07.2021
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Summary:The lack of high throughput screening (HTS) techniques for small molecules that stabilize DNA iMs limits their development as perspective drug candidates. Here we showed that fluorescence monitoring for probing the effects of ligands on the iM stability using the FAM-BHQ1 pair provides incorrect results due to additional dye-related interactions. We developed an alternative system with fluorescent phenoxazine pseudonucleotides in loops that do not alter iM unfolding. At the same time, the fluorescence of phenoxazine residues is sensitive to iM unfolding that enables accurate evaluation of ligand-induced changes of iM stability. Our results provide the basis for new approaches for HTS of iM ligands. A fluorescence-tracking system with phenoxazine pseudonucleotides in loops that do not alter iM unfolding enables precise evaluation of ligand-induced changes of iM stability.
Bibliography:Electronic supplementary information (ESI) available: Experimental details and supporting data. See DOI
10.1039/d1an00660f
ObjectType-Article-1
SourceType-Scholarly Journals-1
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ISSN:0003-2654
1364-5528
DOI:10.1039/d1an00660f