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Induction of DNA doublestrand-breaks along the tracks of low energy protons

机译:沿着低能质子的轨道诱导DNA双链断裂

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With the setup presented here, it is possible to investigate the effects of densely ionising protons in the range of their bragg peak and the repair of the induced concentrated DNA damage. Primary human fibroblasts were irradiated with low energy protons at the Erlangen Tandem Van-de-Graaff accelerator. The DNA damage along the paths of the protons in the cell nuclei was visualised by immunostaining and fluorescence microscopy. The marker protein for the detection of doublestrand breaks was the phosphorylated histon y-H2AX. Clearly identifiable particle tracks could be induced, allowing further investigations of the repair kinetics. While other experiments in this field mostly make use of heavy ions, this works allows the comparison of the results with the effects of densely ionising protons.
机译:通过此处介绍的设置,有可能研究布拉格离子峰范围内的密集电离质子的影响以及诱导的浓缩DNA损伤的修复。在Erlangen Tandem Van-de-Graaff加速器上用低能质子辐照初级人类成纤维细胞。沿细胞核质子路径的DNA损伤通过免疫染色和荧光显微镜观察。用于检测双链断裂的标记蛋白是磷酸化的histon y-H2AX。可以诱导出清晰可辨的颗粒轨迹,从而可以进一步研究修复动力学。尽管该领域的其他实验主要利用重离子,但这项工作可以将结果与密集电离质子的效果进行比较。

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