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What tunes guanine ionization potential in a nucleosome ? An all-in-one systematic QM/MM assessment.
Kermarrec, Maxime; Dumont, Elise; Gillet, Natacha.
Afiliação
  • Kermarrec M; ENSL, CNRS, Laboratoire de Chimie UMR 5182, 46 allée d'Italie, 69364 Lyon France.
  • Dumont E; Université Côte d'Azur, CNRS, Institut de Chimie de Nice, UMR 7272 - 06108 Nice, France; Institut Universitaire de France, 5 rue Descartes, 75005 Paris, France.
  • Gillet N; ENSL, CNRS, Laboratoire de Chimie UMR 5182, 46 allée d'Italie, 69364 Lyon France. Electronic address: natacha.gillet@ens-lyon.fr.
Biophys J ; 2024 Jul 10.
Article em En | MEDLINE | ID: mdl-38988071
ABSTRACT
Guanine radical cations are precursors to oxidatively-induced DNA lesions and the determination of oxidative DNA hot spots beyond oligonucleotides remains a current challenge. In order to rationalize the finetuned ionization properties of the ∼60 guanines in a nucleosome core particle (NCP), we report a robust MD-then-FO-DFTB/MM simulation protocol spanning 20 microseconds. Our work allows to identify several factors governing guanine ionization potential and to map oxidative hotspots. Our results highlight the predominant role of the proximity of positively-charged histone residues in the modulation of the guanine ionization potential up to 0.6 eV. Consequently, fast long range hole transfer in nucleosomal DNA might vary on the proximity of histone tails, so, on a biological point of view, on the chromatin state.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article