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関連する概念動画

Fixing Double-strand Breaks02:04

Fixing Double-strand Breaks

16.0K
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...
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Overview of DNA Repair02:25

Overview of DNA Repair

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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...
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DNA Topoisomerases02:02

DNA Topoisomerases

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Topoisomerases are enzymes that relax overwound DNA molecules during various cell processes, including DNA replication and transcription. These enzymes regulate positive and negative DNA supercoiling without changing the nucleotide sequence. DNA overwinding in a clockwise direction results in positively supercoiled DNA, whereas underwinding in a counterclockwise direction produces negatively supercoiled DNA.
Types and Mechanism of action
Topoisomerases are divided into two main types. ...
37.2K
Nucleosome Remodeling02:54

Nucleosome Remodeling

11.6K
Nucleosomes are the basic units of chromatin compaction. Each nucleosome consists of the DNA bound tightly around a histone core, which makes the DNA inaccessible to DNA binding proteins such as DNA polymerase and RNA polymerase. Hence, the fundamental problem is to ensure access to DNA when appropriate, despite the compact and protective chromatin structure.
Nucleosome remodeling complex
Eukaryotic cells have specialized enzymes called ATP-dependent nucleosome remodeling enzymes. These enzymes...
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Restarting Stalled Replication Forks02:37

Restarting Stalled Replication Forks

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DNA replication is initiated at sites containing predefined DNA sequences known as origins of replication. DNA is unwound at these sites by the minichromosome maintenance (MCM) helicase and other factors such as Cdc45 and the associated GINS complex.The unwound single strands are protected by replication protein A (RPA) until DNA polymerase starts synthesizing DNA at the 5’ end of the strand in the same direction as the replication fork. To prevent the replication fork from falling apart,...
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Entropy within the Cell01:22

Entropy within the Cell

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A living cell's primary tasks of obtaining, transforming, and using energy to do work may seem simple. However, the second law of thermodynamics explains why these tasks are harder than they appear. None of the energy transfers in the universe are completely efficient. In every energy transfer, some amount of energy is lost in a form that is unusable. In most cases, this form is heat energy. Thermodynamically, heat energy is defined as the energy transferred from one system to another that...
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Updated: Mar 20, 2026

High-Resolution Neutron Spectroscopy to Study Picosecond-Nanosecond Dynamics of Proteins and Hydration Water
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DNAの水分化シェルの動的障害

Elise Duboué-Dijon1,2, Aoife C Fogarty1,2, James T Hynes1,2,3

  • 1École Normale Supérieure, PSL Research University, UPMC Univ Paris 06, CNRS, Département de Chimie, PASTEUR, 24 rue Lhomond, 75005 Paris, France.

Journal of the American Chemical Society
|May 31, 2016
PubMed
まとめ
この要約は機械生成です。

DNAの近くの水の動態は複雑で 溝の形とDNAの動きに影響されます これらの要因はDNAにとって重要な 独特の水分殻の振る舞いを生み出します

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Studying DNA Looping by Single-Molecule FRET
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Studying DNA Looping by Single-Molecule FRET

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Structure-Based Simulation and Sampling of Transcription Factor Protein Movements along DNA from Atomic-Scale Stepping to Coarse-Grained Diffusion
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Structure-Based Simulation and Sampling of Transcription Factor Protein Movements along DNA from Atomic-Scale Stepping to Coarse-Grained Diffusion

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関連する実験動画

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High-Resolution Neutron Spectroscopy to Study Picosecond-Nanosecond Dynamics of Proteins and Hydration Water
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Structure-Based Simulation and Sampling of Transcription Factor Protein Movements along DNA from Atomic-Scale Stepping to Coarse-Grained Diffusion
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科学分野:

  • バイオ物理学
  • コンピュータ生物学
  • 構造生物学

背景:

  • DNAの水分化シェルに含まれる水分は 生物化学的機能に不可欠です
  • DNAの生物学的な役割の 鍵となるものです

研究 の 目的:

  • 水分子の方向転換と水素結合のダイナミクスをB-DNAデデカメアの水分化シェルで調査する.
  • 水分化シェルダイナミクスの異質性の源を明示する.

主な方法:

  • 分子力学シミュレーション
  • 分析ジャンプモデル
  • 空間と時間の異質性の分析

主要な成果:

  • DNAトポグラフィとH結合に関連した水分化シェルダイナミクスにおける空間的異質性を特定した.
  • マイナー・グリューブの水動力が 大きく低下した.
  • 発見されたDNA構造の変動は 水のダイナミクスを調節します 特にマイナー・グルーヴで

結論:

  • 生物分子構造の変動は 閉じ込められたDNAの場所での水の動きに不可欠です
  • DNAダイナミクスより速い水分化シェルダイナミクスの仮定は無効です.
  • DNAの溝のダイナミクスは水中結合の再配置に直接影響し,加速する.