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首页> 外文期刊>International Journal of Radiation Biology: Covering the Physical, Chemical, Biological, and Medical Effects of Ionizing and Non-ionizing Radiations >Critical energies for ssb and dsb induction in plasmid DNA by vacuum-UV photons: an arrangement for irradiating dry or hydrated DNA with monochromatic photons.
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Critical energies for ssb and dsb induction in plasmid DNA by vacuum-UV photons: an arrangement for irradiating dry or hydrated DNA with monochromatic photons.

机译:真空紫外光子在质粒DNA中诱导ssb和dsb的关键能量:用单色光子照射干燥或水合DNA的装置。

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摘要

PURPOSE: Theoretical modelling techniques are often used to simulate the action of ionizing radiations on cells at the nanometre level. Using monoenergetic vacuum-UV (VUV) radiation to irradiate DNA either dry or humidified, the action spectra for the induction of DNA damage by low energy photons and the role of water and can be studied. These data provide inputs for the theoretical models. METHODS: Various combinations of monochromator, grating and VUV window have been used to obtain monochromatic photons from the 2 GeV electron synchrotron at the CLRC, Daresbury Laboratory. A sample chamber containing plasmid DNA is installed at the end of the beamline. The chamber can be evacuated or water can be introduced (as water vapour or humidified helium). In this way, DNA can be irradiated either dry or humidified. RESULTS: An arrangement for irradiating dry or humidified DNA using monoenergetic photons from 7 eV to 150 eV has been developed. At the energies used, exposure rates vary from about 5 x 10(10) to 3 x 10(12) photons cm(-2) s(-1) over a 1 cm2 sample area. At all but the lowest energies this is sufficient to produce significant levels of DNA damage in just a few minutes. The measured dose variation over the sample area is typically 30%, but this is reduced significantly using sample scanning techniques.
机译:目的:理论建模技术通常用于模拟电离辐射在纳米水平上对细胞的作用。使用单能真空UV(VUV)辐射干燥或加湿的DNA,可以研究低能光子诱导DNA损伤的作用谱以及水的作用。这些数据为理论模型提供了输入。方法:在达勒斯伯里实验室的CLRC上,单色仪,光栅和VUV窗口的各种组合已用于从2 GeV电子同步加速器获得单色光子。包含质粒DNA的样品室安装在光束线的末端。可以将腔室抽成真空,也可以引入水(作为水蒸气或加湿的氦气)。这样,可以干燥或加湿地照射DNA。结果:已经开发了一种使用7 eV至150 eV的单能光子辐照干燥或加湿的DNA的装置。在使用的能量下,在1平方厘米的样本区域上,曝光速率从5 x 10(10)到3 x 10(12)个光子cm(-2)s(-1)变化。除了最低的能量外,这几乎足以在短短几分钟内对DNA造成严重破坏。在整个样品区域上测得的剂量变化通常为30%,但是使用样品扫描技术可以显着减少这种变化。

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