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原子内壳层弛豫在光子诱导的DNA损伤中的作用。

The role of atomic inner shell relaxations for photon-induced DNA damage.

作者信息

Bernhardt Philipp, Friedland Werner, Paretzke Herwig G

机构信息

GSF-National Research Center for Environment and Health, Institute of Radiation Protection, 85764 Neuherberg, Germany.

出版信息

Radiat Environ Biophys. 2004 Jul;43(2):77-84. doi: 10.1007/s00411-004-0238-7. Epub 2004 Jul 2.

Abstract

The influence of relaxations of atoms making up the DNA and atoms attached to it on radiation-induced cellular DNA damage by photons was studied by very detailed Monte Carlo track structure calculations, as an unusually high importance of inner shell ionizations for biological action was suspected from reports in the literature. For our calculations cross sections for photons and electrons for inner shell orbitals were newly derived and integrated into the biophysical track structure simulation programme PARTRAC. Both the local energy deposition in a small sphere around the interacting relaxed atom, and the number of relaxations per Gy and Gbp were calculated for several target geometries and many monoenergetic photon irradiations. Elements with the highest order number yielded the largest local energy deposition after interaction. The atomic relaxation after ionization of the L1 shell was found to be more biologically efficient than that of the K shell for high Z atoms. Generally, the number of inner shell relaxations produced by photon irradiation was small in comparison to the total number of double strand breaks generated by such radiation. Furthermore, the energy dependence of the total number of photon-induced and electron-induced relaxations at the DNA atoms does not agree with observed RBE values for different biological endpoints. This suggests that the influence of inner shell relaxations of DNA atoms on radiation-induced DNA damage is in general rather small.

摘要

通过非常详细的蒙特卡罗径迹结构计算,研究了构成DNA的原子及其附着原子的弛豫对光子辐射诱导的细胞DNA损伤的影响。因为从文献报道中怀疑内壳层电离对生物作用具有异常高的重要性,所以在我们的计算中,新推导了内壳层轨道的光子和电子截面,并将其整合到生物物理径迹结构模拟程序PARTRAC中。针对几种靶几何结构和许多单能光子辐照,计算了相互作用的弛豫原子周围小球体中的局部能量沉积,以及每Gy和每Gbp的弛豫次数。原子序数最高的元素在相互作用后产生的局部能量沉积最大。对于高Z原子,发现L1壳层电离后的原子弛豫在生物学上比K壳层的更有效。一般来说,与这种辐射产生的双链断裂总数相比,光子辐照产生的内壳层弛豫次数较少。此外,DNA原子处光子诱导和电子诱导的弛豫总数的能量依赖性与不同生物学终点观察到的RBE值不一致。这表明DNA原子的内壳层弛豫对辐射诱导的DNA损伤的影响通常相当小。

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