Fluorescent Oligonucleotide Probes for Screening High-Affinity Nucleobase Surrogates




Aro-Heinila A, Lönnberg T

PublisherWILEY-V C H VERLAG GMBH

2017

Chemistry - A European Journal

CHEMISTRY-A EUROPEAN JOURNAL

CHEM-EUR J

23

5

1028

1031

4

0947-6539

1521-3765

DOIhttps://doi.org/10.1002/chem.201605300

https://research.utu.fi/converis/portal/detail/Publication/28146226



Double-helical oligonucleotide probes featuring a single-nucleotide gap opposed by one of the canonical nucleobases and flanked by the fluorescent nucleobase analogue pyrrolocytosine have been synthesized and titrated with PdII chelates of dipicolinamide and its N-2, N-6-di-alkylated derivatives. The fluorometric titrations revealed greatly increased affinity of the PdII chelates for the nucleobases opposing the gap compared to the respective free nucleotides in solution. Owing to the constrained environment of the single-nucleotide gap, the relative stabilities of the various PdII-mediated base pairs were also significantly different from those previously reported at monomer level.

Last updated on 2024-26-11 at 19:59