Published April 2006 | Version v1
Journal article

Methods for quantitative evaluation of dynamics of repair proteins within irradiated cells

  • 1. Angewandte Physik und Messtechnik LRT2, UniBw-Muenchen, 85577 Neubiberg (Germany)
  • 2. Physik Department E12, TU-Muenchen, 85748 Garching (Germany)
  • 3. Department Biologie II, LMU-Muenchen, 82152 Martinsried (Germany)
  • 4. Strahlenbiologisches Institut, LMU-Muenchen, 80336 Munich (Germany)

Description

Living HeLa cells are irradiated well directed with single 100 MeV oxygen ions by the superconducting ion microprobe SNAKE, the Superconducting Nanoscope for Applied Nuclear (=Kern-) Physics Experiments, at the Munich 14 MV tandem accelerator. Various proteins, which are involved directly or indirectly in repair processes, accumulate as clusters (so called foci) at DNA-double strand breaks (DSBs) induced by the ions. The spatiotemporal dynamics of these foci built by the phosphorylated histone γ-H2AX are studied. For this purpose cells are irradiated in line patterns. The γ-H2AX is made visible under the fluorescence microscope using immunofluorescence techniques. Quantitative analysis methods are developed to evaluate the data of the microscopic images in order to analyze movement of the foci and their changing size

Additional details

Identifiers

DOI
10.1016/j.nimb.2005.11.118;
PII
S0168-583X(05)02062-8;

Publishing Information

Journal Title
Nuclear Instruments and Methods in Physics Research. Section B, Beam Interactions with Materials and Atoms
Journal Volume
245
Journal Issue
1
Journal Page Range
p. 298-301
ISSN
0168-583X
CODEN
NIMBEU

Conference

Title
6. international symposium on swift heavy ions in matter
Acronym
SHIM 2005
Dates
28-31 May 2005
Place
Aschaffenburg (Germany)

Optional Information

Copyright
Copyright (c) 2005 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.