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Molecular dynamics simulation of clustered DNA damage sites containing 8‐oxoguanine and abasic site
Author(s) -
Fujimoto Hirofumi,
Pinak Miroslav,
Nemoto Toshiyuki,
O'Neill Peter,
Kume Etsuo,
Saito Kimiaki,
Maekawa Hideaki
Publication year - 2005
Publication title -
journal of computational chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.907
H-Index - 188
eISSN - 1096-987X
pISSN - 0192-8651
DOI - 10.1002/jcc.20184
Subject(s) - ap site , dna damage , molecular dynamics , dna , dna repair , biophysics , chemistry , xrcc1 , base pair , dna (apurinic or apyrimidinic site) lyase , biology , biochemistry , gene , computational chemistry , genotype , single nucleotide polymorphism
Clustered DNA damage sites induced by ionizing radiation have been suggested to have serious consequences to organisms, such as cancer, due to their reduced probability to be repaired by the enzymatic repair machinery of the cell. Although experimental results have revealed that clustered DNA damage sites effectively retard the efficient function of repair enzymes, it remains unclear as to what particular factors influence this retardation. In this study, approaches based on molecular dynamics (MD) simulation have been applied to examine conformational changes and energetic properties of DNA molecules containing clustered damage sites consisting of two lesioned sites, namely 7,8‐dihydro‐8‐oxoguanine (8‐oxoG) and apurinic/apyrimidinic (AP) site, located within a few base pairs of each other. After 1 ns of MD simulation, one of the six DNA molecules containing a clustered damage site develops specific characteristic features: sharp bending at the lesioned site and weakening or complete loss of electrostatic interaction energy between 8‐oxoG and bases located on the complementary strand. From these results it is suggested that these changes would make it difficult for the repair enzyme to bind to the lesions within the clustered damage site and thereby result in a reduction of its repair capacity. © 2005 Wiley Periodicals, Inc. J Comput Chem 26: 788–798, 2005