Vyšín Luděk, Pachnerová Brabcová Kateřina, Štěpán Václav, Moretto-Capelle Patrick, Bugler Beatrix, Legube Gaelle, Cafarelli Pierre, Casta Romain, Champeaux Jean Philippe, Sence Martine, Vlk Martin, Wagner Richard, Štursa Jan, Zach Václav, Incerti Sebastien, Juha Libor, Davídková Marie
Institute of Physics CAS, Na Slovance 1999/2, 182 21, Prague, Czech Republic.
Radiat Environ Biophys. 2015 Aug;54(3):343-52. doi: 10.1007/s00411-015-0605-6. Epub 2015 May 26.
Clustered DNA damage induced by 10, 20 and 30 MeV protons in pBR322 plasmid DNA was investigated. Besides determination of strand breaks, additional lesions were detected using base excision repair enzymes. The plasmid was irradiated in dry form, where indirect radiation effects were almost fully suppressed, and in water solution containing only minimal residual radical scavenger. Simultaneous irradiation of the plasmid DNA in the dry form and in the solution demonstrated the contribution of the indirect effect as prevalent. The damage composition slightly differed when comparing the results for liquid and dry samples. The obtained data were also subjected to analysis concerning different methodological approaches, particularly the influence of irradiation geometry, models used for calculation of strand break yields and interpretation of the strand breaks detected with the enzymes. It was shown that these parameters strongly affect the results.
研究了10、20和30兆电子伏质子在pBR322质粒DNA中诱导产生的聚集性DNA损伤。除了测定链断裂外,还使用碱基切除修复酶检测了其他损伤。质粒以干燥形式进行辐照,此时间接辐射效应几乎被完全抑制,同时也在仅含有微量残留自由基清除剂的水溶液中进行辐照。对干燥形式和溶液中的质粒DNA同时进行辐照表明,间接效应起主要作用。比较液体和干燥样品的结果时,损伤组成略有不同。还对所得数据进行了不同方法学途径的分析,特别是辐照几何形状的影响、用于计算链断裂产率的模型以及用酶检测到的链断裂的解释。结果表明,这些参数对结果有很大影响。