Electronic pathways in photoactivated repair of UV mutated DNA

An investigation of the physics, underlying the damage caused to DNA by UV radiation and its subsequent repair via a photoreactivation mechanism, is presented in this study. Electronic pathways, starting from the initial damage to the final repair process, are presented. UV radiation is absorbed to...

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Main Authors: Bohr, H., Jalkanen, Karl, Malik, F.
Format: Journal Article
Published: World Scientific Publishing Company 2005
Subjects:
Online Access:http://hdl.handle.net/20.500.11937/18557
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author Bohr, H.
Jalkanen, Karl
Malik, F.
author_facet Bohr, H.
Jalkanen, Karl
Malik, F.
author_sort Bohr, H.
building Curtin Institutional Repository
collection Online Access
description An investigation of the physics, underlying the damage caused to DNA by UV radiation and its subsequent repair via a photoreactivation mechanism, is presented in this study. Electronic pathways, starting from the initial damage to the final repair process, are presented. UV radiation is absorbed to create a hole-excited thymine or other pyrimidine that subsequently is responsible for the formation of a dimer. The negative-ion of the cofactor riboflavin, FADH-, formed by the exposure of the photolyase protein to visible light, interacts with the hole-excited electronic orbital of the thymine dimer inducing a photon-less Auger transition, which restores the two thymines to the ground state, thereby detaching the lesion and repairing the DNA. Density functional theoretical calculations supporting the theory are presented. The mechanism involves the least amount of energy dissipation and is charge neutral. It also avoids radiation damage in the repair process. Recent experimental data are compatible with this theory.
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institution Curtin University Malaysia
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publishDate 2005
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spelling curtin-20.500.11937-185572018-03-29T09:06:21Z Electronic pathways in photoactivated repair of UV mutated DNA Bohr, H. Jalkanen, Karl Malik, F. continuum Auger processes isomers density functional theory (DFT) photolyase intersystem crossing electronic excited states thymine dimer UV-activated thymine An investigation of the physics, underlying the damage caused to DNA by UV radiation and its subsequent repair via a photoreactivation mechanism, is presented in this study. Electronic pathways, starting from the initial damage to the final repair process, are presented. UV radiation is absorbed to create a hole-excited thymine or other pyrimidine that subsequently is responsible for the formation of a dimer. The negative-ion of the cofactor riboflavin, FADH-, formed by the exposure of the photolyase protein to visible light, interacts with the hole-excited electronic orbital of the thymine dimer inducing a photon-less Auger transition, which restores the two thymines to the ground state, thereby detaching the lesion and repairing the DNA. Density functional theoretical calculations supporting the theory are presented. The mechanism involves the least amount of energy dissipation and is charge neutral. It also avoids radiation damage in the repair process. Recent experimental data are compatible with this theory. 2005 Journal Article http://hdl.handle.net/20.500.11937/18557 10.1142/S021798490500844X World Scientific Publishing Company restricted
spellingShingle continuum Auger processes
isomers
density functional theory (DFT)
photolyase
intersystem crossing
electronic excited states
thymine dimer
UV-activated thymine
Bohr, H.
Jalkanen, Karl
Malik, F.
Electronic pathways in photoactivated repair of UV mutated DNA
title Electronic pathways in photoactivated repair of UV mutated DNA
title_full Electronic pathways in photoactivated repair of UV mutated DNA
title_fullStr Electronic pathways in photoactivated repair of UV mutated DNA
title_full_unstemmed Electronic pathways in photoactivated repair of UV mutated DNA
title_short Electronic pathways in photoactivated repair of UV mutated DNA
title_sort electronic pathways in photoactivated repair of uv mutated dna
topic continuum Auger processes
isomers
density functional theory (DFT)
photolyase
intersystem crossing
electronic excited states
thymine dimer
UV-activated thymine
url http://hdl.handle.net/20.500.11937/18557