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Molecular Dynamics Insights into Polyamine–DNA Binding Modes: Implications for Cross‐Link Selectivity
Author(s) -
Big Emmanuelle,
Chan ChenHui,
Morell Christophe,
Monari Antonio,
Ravanat JeanLuc,
Dumont Elise
Publication year - 2017
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201702065
Subject(s) - chemistry , polyamine , guanine , molecular dynamics , nucleobase , spermine , dna , accessible surface area , stereochemistry , dna condensation , spermidine , crystallography , biophysics , computational chemistry , nucleotide , biochemistry , enzyme , transfection , biology , gene
Biogenic polyamines, which play a role in DNA condensation and stabilization, are ubiquitous and are found at millimolar concentration in the nucleus of eukaryotic cells. The interaction modes of three polyamines—putrescine (Put), spermine (Spm), and spermidine (Spd)—with a self‐complementary 16 base pair (bp) duplex, are investigated by all‐atom explicit‐solvent molecular dynamics. The length of the amine aliphatic chain leads to a change of the interaction mode from minor groove binding to major groove binding. Through all‐atom dynamics, noncovalent interactions that stabilize the polyamine–DNA complex and prefigure the reactivity, leading to the low‐barrier formation of deleterious DNA–polyamine cross‐links, after one‐electron oxidation of a guanine nucleobase, are unraveled. The binding strength is quantified from the obtained trajectories by molecular mechanics generalized Born surface area post‐processing (MM‐GBSA). The values of binding free energies provide the same affinity order, Put