Open Access8-Oxoguanine Forms Quartets with a Large Central Cavity
Author(s) -
Simon Aleksič,
Peter Podbevšek,
Janez Plavec
Publication year - 2022
Publication title -
biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.43
H-Index - 253
eISSN - 1520-4995
pISSN - 0006-2960
DOI - 10.1021/acs.biochem.2c00478
Subject(s) - nucleobase , guanine , phosphodiester bond , chemistry , nucleic acid , dna , nucleotide , hydrogen bond , base pair , stereochemistry , g quadruplex , rna , crystallography , biochemistry , molecule , gene , organic chemistry
Oxidation of a guanine nucleotide in DNA yields an 8-oxoguanine nucleotide ( oxo G) and is a mutagenic event in the genome. Due to different arrangements of hydrogen-bond donors and acceptors, oxo G can affect the secondary structure of nucleic acids. We have investigated base pairing preferences of oxo G in the core of a tetrahelical G-quadruplex structure, adopted by analogues of d(TG 4 T). Using spectroscopic methods, we have shown that G-quartets can be fully substituted with oxo G nucleobases to form an oxo G-quartet with a revamped hydrogen-bonding scheme. While an oxo G-quartet can be incorporated into the G-quadruplex core without distorting the phosphodiester backbone, larger dimensions of the central cavity change the cation localization and exchange properties.