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2,6‐Dimercuriphenol as a Bifacial Dinuclear Organometallic Nucleobase
Author(s) -
Ukale Dattatraya Uttam,
Lönnberg Tuomas
Publication year - 2018
Publication title -
angewandte chemie
Language(s) - English
Resource type - Journals
eISSN - 1521-3757
pISSN - 0044-8249
DOI - 10.1002/ange.201809398
Subject(s) - nucleobase , triple helix , uracil , pyrimidine , thymine , oligonucleotide , cytosine , chemistry , moiety , stereochemistry , dna , base pair , nucleoside , nucleic acid , guanine , ap site , nucleotide , biochemistry , dna damage , gene
A C ‐nucleoside having 2,6‐dimercuriphenol as the base moiety has been synthesized and incorporated into an oligonucleotide. NMR and UV melting experiments revealed the ability of this bifacial organometallic nucleobase surrogate to form stable dinuclear Hg II ‐mediated base triples with adenine, cytosine, and thymine (or uracil) in solution as well as within a triple‐helical oligonucleotide. A single Hg II ‐mediated base triple between 2,6‐dimercuriphenol and two thymines increased both Hoogsteen and Watson–Crick melting temperatures of a 15‐mer pyrimidine⋅purine*pyrimidine triple helix by more than 10 °C relative to an unmodified triple helix of the same length. This novel binding mode could be exploited in targeting certain pathogenic nucleic acids as well as in DNA nanotechnology.