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The Influence of Single Tandem and Clustered DNA Damage on the Electronic Properties of the Double Helix: A Theoretical Study

机译:单次串联和聚类DNA损伤对双螺旋电子性质的影响:理论研究

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摘要

Oxidatively generated damage to DNA frequently appears in the human genome as the effect of aerobic metabolism or as the result of exposure to exogenous oxidizing agents, such as ionization radiation. In this paper, the electronic properties of single, tandem, and clustered DNA damage in comparison with native -DNA are discussed as a comparative analysis for the first time. A single lesion—8-oxo-7,8-dihydro-2′-deoxyguanosine (G ), a tandem lesion—(5′ ) and (5′ ) 5′,8-cyclo-2′-deoxyadenosine (cdA), and the presence of both of them in one helix turn as clustered DNA damage were chosen and taken into consideration. The lowest vertical and adiabatic potential (VIP ~ 5.9 and AIP ~ 5.5 eV, respectively) were found for G , independently of the discussed DNA lesion type and their distribution within the double helix. Moreover, the VIP and AIP were assigned for -trimers, - dimers and single base pairs isolated from parental -hexamers in their neutral and cationic forms. The above results were confirmed by the charge and spin density population, which revealed that G can be considered as a cation radical point of destination independently of the DNA damage type (single, tandem, or clustered). Additionally, the different influences of cdA on the charge transfer rate were found and discussed in the context of tandem and clustered lesions. Because oligonucleotide lesions are effectively produced as a result of ionization factors, the presented data in this article might be valuable in developing a new scheme of anticancer radiotherapy efficiency.
机译:对DNA的氧化产生的损伤经常出现在人类基因组中作为有氧代谢的影响或由于暴露于外源氧化剂的结果,例如电离辐射。本文首次讨论了与天然-DNA相比的单,串联和聚类DNA损伤的电子性质作为对比分析。单个病变-8-氧代-7,8-二氢-2'-脱氧核苷酸(g),串联病变 - (5')和(5')5',8-环-2'-脱氧腺苷(CDA),并且选择了它们在一个螺旋转向螺旋变为聚类DNA损伤的情况下,并考虑它们。对于G,可以独立于讨论的DNA病变类型及其在双螺旋内的分布,发现了G的最低垂直和绝热势(vip〜5.9和aip〜5.5ev)。此外,将VIP和AIP分配用于 - 中性和阳离子形式的父母 - 己烯分离的细胞,二聚体和单碱基对。通过电荷和旋转密度群证实了上述结果,其显示,G可以被认为是独立于DNA损伤型(单,串联或聚类)的阳离子直接目的地。另外,在串联和聚类病变的背景下发现并讨论了CDA对电荷转移率的不同影响。由于由于电离因子有效地生产了寡核苷酸病变,所以本文中所呈现的数据可能是在开发抗癌放疗效率的新方案方案中有价值。

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