Radiology and Imaging Sciences, Clinical Center, NIH, Bethesda, Maryland 20892, USA.
Radiat Res. 2010 Jan;173(1):98-109. doi: 10.1667/RR1865.1.
Auger electron emitters like (125)I are the radionuclides of choice for gene-targeted radiotherapy. The highly localized damage they induce in DNA is produced by three mechanisms: direct damage by the emitted Auger electrons, indirect damage by diffusible free radicals produced by Auger electrons traveling in water, and charge neutralization of the residual, highly positively charged tellurium daughter atom by stripping electrons from covalent bonds of neighboring residues. The purpose of our work was to determine whether these mechanisms proceed through an intermediate energy transfer step along DNA. It was proposed that this intermediate step proceeds through the charge transport mechanism in DNA. Conventional charge transport has been described as either a hopping mechanism initiated by charge injection into DNA and propagated by charge migration along the DNA or a tunneling mechanism in which charge moves directly from a donor to an acceptor within DNA. Well-known barriers for the hopping mechanism were used to probe the role of charge transport in (125)I-induced DNA damage. We studied their effect on the distribution of DNA breaks produced by the decay of (125)I in samples frozen at -80 degrees C. We found that these barriers had no measurable effect on the distribution of (125)I-induced breaks.
(125)I 等俄歇电子发射体是基因靶向放射治疗中首选的放射性核素。 它们在 DNA 中诱导的高度局部损伤是通过三种机制产生的:发射的俄歇电子直接损伤、在水中传播的俄歇电子产生的可扩散自由基的间接损伤,以及通过从相邻残基的共价键中剥离电子来中和残留的、带高度正电荷的碲子原子的电荷中和。我们的工作目的是确定这些机制是否通过 DNA 中的中间能量转移步骤进行。有人提出,这个中间步骤是通过 DNA 中的电荷传输机制进行的。传统的电荷传输被描述为电荷注入到 DNA 中引发的跳跃机制,或者是电荷在 DNA 中直接从供体移动到受体的隧道机制。我们使用众所周知的跳跃机制障碍来探测电荷传输在(125)I 诱导的 DNA 损伤中的作用。我们研究了它们对在-80°C 冷冻样品中(125)I 衰变产生的 DNA 断裂分布的影响。我们发现这些障碍对(125)I 诱导的断裂分布没有可测量的影响。