Radiosensitivity of DNA in a specific protein-DNA complex: the lac repressor-lac operator complex
Language English Country England, Great Britain Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
- MeSH
- Bacterial Proteins chemistry radiation effects MeSH
- DNA, Bacterial chemistry genetics radiation effects MeSH
- Escherichia coli genetics radiation effects MeSH
- Hydroxyl Radical chemistry radiation effects MeSH
- Nucleic Acid Conformation MeSH
- Protein Conformation MeSH
- Lac Operon radiation effects MeSH
- Lac Repressors MeSH
- Macromolecular Substances MeSH
- Monte Carlo Method MeSH
- Models, Molecular MeSH
- Operator Regions, Genetic radiation effects MeSH
- DNA Damage MeSH
- Escherichia coli Proteins * MeSH
- Repressor Proteins chemistry radiation effects MeSH
- Base Sequence MeSH
- Radiation Tolerance MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Bacterial Proteins MeSH
- DNA, Bacterial MeSH
- Hydroxyl Radical MeSH
- Lac Repressors MeSH
- LacI protein, E coli MeSH Browser
- Macromolecular Substances MeSH
- Escherichia coli Proteins * MeSH
- Repressor Proteins MeSH
PURPOSE: To calculate the probability of radiation-induced frank strand breakage (FSB) at each nucleotide in the Escherichia coli lac repressor-lac operator system using a simulation procedure. To compare calculated and experimental results. To asses the contribution of DNA conformational changes and of the masking by the protein to DNA protection by the repressor. MATERIALS AND METHODS: Two structures of the complex were extracted from the PDB databank: crystallography- and NMR-based structures. Calculations were made of the accessibility of the atoms mainly involved in strand breakage (H4' and H5') to O&Hdot; and of the FSB probabilities, along: (1) DNA in the complex; (2) DNA in the complex depleted of the repressor; and (3) a linear DNA having the same sequence. An 80bp fragment bearing the operator was irradiated alone or in presence of the repressor. The relative probabilities of FSB at each nucleotide were determined using sequencing gel electrophoresis. RESULTS: Calculations predict modulation of the accessibility of H4' and H5' atoms and of the probabilities of FSB along the DNA fragments of complexes. This is due to the protein-induced conformational change and to masking by bound protein. The best agreement with the experimental FSB was observed for calculations that use the crystallography-based structure. CONCLUSIONS: For specific DNA-protein complexes, our calculations can predict the protein radiolytic footprints on DNA. They show the significant contribution of the protein-induced DNA conformational change to DNA protection.
References provided by Crossref.org