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利用荧光共振能量转移对固态DNA中电离辐射诱导的无碱基位点进行定位估计。

Localization estimation of ionizing radiation-induced abasic sites in DNA in the solid state using fluorescence resonance energy transfer.

作者信息

Akamatsu Ken, Shikazono Naoya, Saito Takeshi

机构信息

a  Irradiation Cell Analysis Group, Quantum Beam Science Directorate, Kansai Photon Science Institute, Japan Atomic Energy Agency, Kizugawa, Kyoto 619-0215, Japan.

出版信息

Radiat Res. 2015 Jan;183(1):105-13. doi: 10.1667/RR13780.1. Epub 2015 Jan 7.

Abstract

Clustered DNA damage is considered an important factor in determining the biological consequences of ionizing radiation. In this study, we successfully estimated the localization of abasic sites (APs) in DNA exposed to ionizing radiation using fluorescence resonance energy transfer (FRET) without any involvement of repair enzyme functions. A linearized plasmid (pUC19 digested by Sma I) was irradiated with: (60)Co γ rays; (4)He(2+) (2.0 MeV/u) particles; and the (12)C(5+) (0.37 MeV/u) particles in the solid state. A donor or acceptor fluorescent probe with a nucleophilic O-amino group was used to label APs. The results showed that the (12)C(5+) particle likely produced close APs within a track. The apparent distance calculated from the observed FRET efficiency (E) of around 0.10 was estimated to be approximately 17 base pairs. On the other hand, E values of (60)Co γ rays and the (4)He(2+) beam were less than those of the (12)C(5+) beam, increased with increasing AP density (the average number of APs per base pair), and were slightly greater than those of randomly distributed APs. We propose that the FRET method provides a degree of localization regardless of whether an AP cluster is single-stranded or bistranded DNA damage.

摘要

簇状DNA损伤被认为是决定电离辐射生物学后果的一个重要因素。在本研究中,我们成功地利用荧光共振能量转移(FRET)估计了暴露于电离辐射的DNA中无碱基位点(APs)的定位,而无需任何修复酶功能的参与。用以下射线照射线性化质粒(经Sma I消化的pUC19):(60)Coγ射线;(4)He(2+)(2.0 MeV/u)粒子;以及固态的(12)C(5+)(0.37 MeV/u)粒子。使用带有亲核O-氨基的供体或受体荧光探针标记APs。结果表明,(12)C(5+)粒子可能在径迹内产生紧密的APs。根据观察到的约0.10的FRET效率(E)计算出的表观距离估计约为17个碱基对。另一方面,(60)Coγ射线和(4)He(2+)束的E值小于(12)C(5+)束的E值,随AP密度(每碱基对AP的平均数量)增加而增加,且略大于随机分布的APs的E值。我们提出,无论AP簇是单链还是双链DNA损伤,FRET方法都能提供一定程度的定位。

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