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関連する概念動画

DNA Topoisomerases02:02

DNA Topoisomerases

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.  Type I...
Restarting Stalled Replication Forks02:37

Restarting Stalled Replication Forks

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, a...
Homologous Recombination02:31

Homologous Recombination

The basic reaction of homologous recombination (HR) involves two chromatids that contain DNA sequences sharing a significant stretch of identity. One of these sequences uses a strand from another as a template to synthesize DNA in an enzyme-catalyzed reaction. The final product is a novel amalgamation of the two substrates. To ensure an accurate recombination of sequences, HR is restricted to the S and G2 phases of the cell cycle. At these stages, the DNA has been replicated already and the...
The DNA Replication Fork01:02

The DNA Replication Fork

An organism’s genome needs to be duplicated in an efficient and error-free manner for its growth and survival. The replication fork is a Y-shaped active region where two strands of DNA are separated and replicated continuously. The coupling of DNA unzipping and complementary strand synthesis is a characteristic feature of a replication fork.   Organisms with small circular DNA, such as E. coli, often have a single origin of replication; therefore, they have only two replication forks, one in...
Residual Stresses01:26

Residual Stresses

Residual stresses reside in a structure even after removing the original stress inducer. This phenomenon often arises from varied plastic deformations across different parts of a structure. Consider a rod stretched beyond its yield point. It will not regain its original length due to permanent deformation. Even after load removal, the rod does not entirely lose stress because of uneven plastic deformations, resulting in residual stresses. The computation of these stresses in structures is...
DNA as a Genetic Template02:05

DNA as a Genetic Template

Two structural features of the DNA molecule provide a basis for the mechanisms of heredity: the four nucleotide bases and its double-stranded nature. The Watson-Crick model of double-helical DNA structure, proposed in 1952, drew heavily upon the X-ray crystallography work of researchers Rosalind Franklin and Maurice Wilkins. Watson, Crick, and Wilkins jointly received the Nobel Prize in Physiology or Medicine for their work in 1962. Franklin was, controversially, excluded from the prize for...

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関連する実験動画

Updated: May 25, 2026

Optical Tweezers to Study RNA-Protein Interactions in Translation Regulation
12:26

Optical Tweezers to Study RNA-Protein Interactions in Translation Regulation

Published on: February 12, 2022

再加重された引力シミュレーションからRNAの解き放たれ.

Francesco Colizzi1, Giovanni Bussi

  • 1SISSA-Scuola Internazionale Superiore di Studi Avanzati, via Bonomea 265, 34136 Trieste, Italy. colizzi@sissa.it

Journal of the American Chemical Society
|February 9, 2012
PubMed
まとめ

この研究は,生物学的機能にとって極めて重要なRNA塩基対の開閉の分子動態を明らかにしています. 私たちの発見は,実験によって検証されたヘリックス開きの動きのイメージを提供し,酵素駆動の解き放たれを説明します.

科学分野:

  • 分子生物物理学 分子生物物理学
  • コンピュータ生物学 コンピュータ生物学
  • RNA 生物学 RNA 生物学

背景:

  • RNA塩基対の形成と溶解は,生物学的機能にとって不可欠な構成的移行である.
  • これらのRNAデュプレックストランジションのダイナミックなステップは,分子レベルの定量的な特徴づけが欠けている.

研究 の 目的:

  • 分子レベルでRNA塩基対の開きと融解のダイナミックなステップを定量的に特徴付ける.
  • RNAヘリックス開封の分子映像を提供するために.

主な方法:

  • 基礎開口プロセスを強制するために,原子的引力シミュレーションが使用されました.
  • 溶解のような反応座標に沿った自由エネルギープロフィールを再構築するために,新しい重量付けスキームが開発されました.
  • このアプローチは,異なる塩基対の組み合わせに体系的に適用された.

主要な成果:

  • RNAヘリックス開口の詳細な分子映像が生成されました.
  • ベースペアを開くための自由エネルギープロファイルを再構築しました.
  • 結果は,広範な実験観察によって検証されました.
  • RNAのダイナミクスと酵素に依存する解き放つメカニズムとの間のリンクが確立されました.

さらに関連する動画

Magnetic Tweezers for the Measurement of Twist and Torque
11:41

Magnetic Tweezers for the Measurement of Twist and Torque

Published on: May 19, 2014

Single-Molecule Real-Time Visualization of DNA Unwinding by CMG Helicase
07:37

Single-Molecule Real-Time Visualization of DNA Unwinding by CMG Helicase

Published on: September 27, 2024

関連する実験動画

Last Updated: May 25, 2026

Optical Tweezers to Study RNA-Protein Interactions in Translation Regulation
12:26

Optical Tweezers to Study RNA-Protein Interactions in Translation Regulation

Published on: February 12, 2022

Magnetic Tweezers for the Measurement of Twist and Torque
11:41

Magnetic Tweezers for the Measurement of Twist and Torque

Published on: May 19, 2014

Single-Molecule Real-Time Visualization of DNA Unwinding by CMG Helicase
07:37

Single-Molecule Real-Time Visualization of DNA Unwinding by CMG Helicase

Published on: September 27, 2024

結論:

  • RNA複合体の内在のダイナミクスは解明されている.
  • これらのダイナミクスは,RNA処理分子機械で観察された方向性を合理化することができます.
  • この研究は,RNAの構成の変化を理解するための分子基盤を提供します.