過剰な電子が溶解DNA核酸と相互作用する: 鎖の断裂は室温で可能です
1Atomistic Simulation Centre, Queen's University Belfast, UK.
Journal of the American Chemical Society
|May 22, 2012
まとめ
イオン化する放射線によって生成される低エネルギー電子は,DNA鎖の断裂を引き起こす可能性があります. 私たちの研究では,DNAにおけるフォスフォディエステル結合の割れ分のための低エネルギーバリアが発見され,このメカニズムを室温でサポートしました.
科学分野:
- バイオフィジックス 生物物理学
- 放射線化学 放射線化学
- 分子生物学は分子生物学である.
背景:
- 離子放射線は,生物物質に低エネルギー電子 (<20 eV) を生成する.
- これらの電子はDNAと相互作用し,核塩基は高い電子親和性を示しています.
- 以前の研究によると,核塩基は,溶解したDNA断片に存在するこれらの余分な電子を惹きつけるという.
研究 の 目的:
- 低エネルギー電子がDNAに及ぼす長期的な影響を調査する.
- ソルバット核酸におけるフォスフォディエステルC(3') - O(3') 結合割れのための自由エネルギーバリアを決定する.
- 低エネルギー電子がDNA鎖の断裂を誘発する可能性を評価する.
主な方法:
- 第一原則 計算的研究.
- 完全溶解核酸における結合分裂のための自由エネルギーバリアの計算.
- 電子誘発によるDNA損傷メカニズムの分析.
主要な成果:
- フォスフォディエステルC(3') -O(3') 結合割れのための自由エネルギーバリアは,ソルバテド核酸素のために計算されました.
- デオキシアデノシンモノフォスファート (dAMP) を除けば,バリアは約6kcal/molでした.
- これらの低いバリアは,溶媒と熱の変動による300Kでの定期的な結合割れを示唆しています.
結論:
- 低エネルギー電子は,DNA鎖の断裂につながる可能性があります.
- フォスフォディエステルC(3') -O(3') 結合の割れは,その可能性が高い結果である.
- 研究結果は,DNA損傷における低エネルギー電子の役割を支持しています.
関連する概念動画
Fixing Double-strand Breaks
The double-stranded structure of DNA has two major advantages. First, it serves as a safe repository of genetic information where one strand serves as the back-up in case the other strand is damaged. Second, the double-helical structure can be wrapped around proteins called histones to form nucleosomes, which can then be tightly wound to form chromosomes. This way, DNA chains up to 2 inches long can be contained within microscopic structures in a cell. A double-stranded break not only damages...
Fixing Double-strand Breaks
The double-stranded structure of DNA has two major advantages. First, it serves as a safe repository of genetic information where one strand serves as the back-up in case the other strand is damaged. Second, the double-helical structure can be wrapped around proteins called histones to form nucleosomes, which can then be tightly wound to form chromosomes. This way, DNA chains up to 2 inches long can be contained within microscopic structures in a cell. A double-stranded break not only damages...
Nucleotide Excision Repair
Overview
Nucleotide Excision Repair
DNA Distortion and Damage
Cells are regularly exposed to mutagens—factors in the environment that can damage DNA and generate mutations. UV radiation is one of the most common mutagens and is estimated to introduce a significant number of changes in DNA. These include bends or kinks in the structure, which can block DNA replication or transcription. If these errors are not fixed, the damage can cause mutations, which in turn can result in cancer or disease depending on which sequences are...
Cells are regularly exposed to mutagens—factors in the environment that can damage DNA and generate mutations. UV radiation is one of the most common mutagens and is estimated to introduce a significant number of changes in DNA. These include bends or kinks in the structure, which can block DNA replication or transcription. If these errors are not fixed, the damage can cause mutations, which in turn can result in cancer or disease depending on which sequences are...
Nucleotide Excision Repair
Overview
Overview of DNA Repair
In order to be passed through generations, genomic DNA must be undamaged and error-free. However, every day, DNA in a cell undergoes several thousand to a million damaging events by natural causes and external factors. Ionizing radiation such as UV rays, free radicals produced during cellular respiration, and hydrolytic damage from metabolic reactions can alter the structure of DNA. Damages caused include single-base alteration, base dimerization, chain breaks, and cross-linkage.
Chemically...
Chemically...


