Simulation of DNA fragment distributions after irradiation with photons
| Autor: | Werner Friedland, Herwig G. Paretzke, Andrea Ottolenghi, Matteo Merzagora, Peter Jacob |
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| Rok vydání: | 1999 |
| Předmět: |
Models
Molecular Biophysics Molecular physics chemistry.chemical_compound medicine Humans Nucleosome Computer Simulation Irradiation General Environmental Science Physics Photons Radiation biology Dose-Response Relationship Radiation Fibroblasts Chromatin Kinetics Histone medicine.anatomical_structure chemistry Helix biology.protein Interphase Atomic physics Monte Carlo Method Nucleus DNA DNA Damage |
| Zdroj: | Radiation and Environmental Biophysics. 38:39-47 |
| ISSN: | 1432-2099 0301-634X |
| DOI: | 10.1007/s004110050136 |
| Popis: | The Monte Carlo track structure code PARTRAC has been further improved by implementing electron scattering cross-sections for liquid water and by explicitly modelling the interaction of water radicals with DNA. The model of the genome inside a human cell nucleus in its interphase is based on the atomic coordinates of the DNA double helix with an additional volume for the water shell. The DNA helix is wound around histone complexes, and these nucleosomes are folded into chromatin fibres and further to fibre loops, which are interconnected to build chromosomes with a territorial organisation. Simulations have been performed for the irradiation of human fibroblast cells with carbon K and aluminium K ultrasoft x-rays, 220 kVp x-rays and 60Co gamma-rays. The ratio single-strand breaks to double-strand breaks (ssb/dsb) for both types of ultrasoft x-rays is lower than for gamma-rays by a factor of 2. The contributions of direct and indirect effects to strand break induction are almost independent of photon energy. Strand break patterns from indirect effects reflect differences in the susceptibility of the DNA helix to OH* attack inside the chromatin fibre. Distributions of small DNA fragments (3 kbp) are determined by the chromatin fibre structure irrespective of whether direct or indirect effects are causing the breaks. In the calculated fragment size distributions for larger DNA fragments (30 kbp), a substantial deviation from random breakage is found only for carbon K irradiation, and is attributed to its inhomogeneous dose distribution inside the cell nucleus. For the other radiation qualities, the results for larger fragments can be approximated by random breakage distributions calculated for a yield of dsb which is about 10% lower than the average for the whole genome. The excess of DNA fragments detected experimentally in the 8-300 kbp region after x-ray irradiation is not seen in our simulation results. |
| Databáze: | OpenAIRE |
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