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相关概念视频

Single-Strand DNA Binding Proteins01:03

Single-Strand DNA Binding Proteins

14.9K
For successful DNA replication, the unwinding of double-stranded DNA must be accompanied by stabilization and protection of the separated single strands of the DNA. This crucial task is performed by single-strand DNA-binding (SSB) proteins. They bind to the DNA in a sequence-independent manner, which means that the nitrogenous bases of the DNA need not be present in a specific order for binding of SSB proteins to it. The binding of SSB proteins straightens single-stranded DNA (ssDNA) and makes...
14.9K
Translesion DNA Polymerases02:10

Translesion DNA Polymerases

10.1K
Translesion (TLS) polymerases rescue stalled DNA polymerases at sites of damaged bases by replacing the replicative polymerase and installing a nucleotide across the damaged site. Doing so, TLS allows additional time for the cell to repair the damage before resuming regular DNA replication.
TLS polymerases are found in all three domains of life - archaea, bacteria, and eukaryotes. Of the different classes of TLS polymerases, members of the Y family are fitted with specialized structures that...
10.1K
The Replisome03:01

The Replisome

34.7K
DNA replication is carried out by a large complex of proteins that act in a coordinated matter to achieve high-fidelity DNA replication. Together this complex is known as the DNA replication machinery or the replisome.
The synthesis of the leading and lagging strands is a highly coordinated process. To explain this, the “Trombone model” was proposed by Bruce Alberts in 1980. The DNA loop formation starts when a primer is synthesized on the parent lagging strand. The loop grows with...
34.7K
Restarting Stalled Replication Forks02:37

Restarting Stalled Replication Forks

5.9K
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,...
5.9K
Proofreading01:31

Proofreading

6.6K
Synthesis of new DNA molecules is carried out by the enzyme DNA polymerase, which adds nucleotides on the daughter strand complementary to the template DNA strand. DNA polymerase has a higher affinity to add the correct base and ensures fidelity during DNA replication. Furthermore,  it exhibits proofreading activity during replication, using an exonuclease domain that cuts off incorrect nucleotides from the nascent DNA strand.
Errors During Replication are Corrected by the DNA Polymerase...
6.6K
Homologous Recombination02:31

Homologous Recombination

52.0K
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...
52.0K

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相关实验视频

Updated: Sep 11, 2025

Single-Molecule Fluorescence Visualization of DNA Polymerase Dynamics at G-Quadruplexes
05:37

Single-Molecule Fluorescence Visualization of DNA Polymerase Dynamics at G-Quadruplexes

Published on: April 4, 2025

841

DNA聚合酶积极且顺序地取代单链DNA结合蛋白.

Longfu Xu1, Shikai Jin2,3, Mia Urem4

  • 1Department of Physics and Astronomy, and LaserLaB Amsterdam, Vrije Universiteit Amsterdam, De Boelelaan 1081, 1081 HV, Amsterdam, The Netherlands.

Nature communications
|August 11, 2025
PubMed
概括

DNA聚合酶 (DNAp) 通过降低它们的解离屏障来取代单链DNA结合蛋白 (SSB),确保高效的DNA复制和基因组完整性.

更多相关视频

Direct Restart of a Replication Fork Stalled by a Head-On RNA Polymerase
07:27

Direct Restart of a Replication Fork Stalled by a Head-On RNA Polymerase

Published on: April 29, 2010

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Strand-Specific Analysis of Proteins at Replicating DNA Strands by Enrichment and Sequencing of Protein-Associated Nascent DNA Method
08:53

Strand-Specific Analysis of Proteins at Replicating DNA Strands by Enrichment and Sequencing of Protein-Associated Nascent DNA Method

Published on: May 2, 2025

482

相关实验视频

Last Updated: Sep 11, 2025

Single-Molecule Fluorescence Visualization of DNA Polymerase Dynamics at G-Quadruplexes
05:37

Single-Molecule Fluorescence Visualization of DNA Polymerase Dynamics at G-Quadruplexes

Published on: April 4, 2025

841
Direct Restart of a Replication Fork Stalled by a Head-On RNA Polymerase
07:27

Direct Restart of a Replication Fork Stalled by a Head-On RNA Polymerase

Published on: April 29, 2010

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Strand-Specific Analysis of Proteins at Replicating DNA Strands by Enrichment and Sequencing of Protein-Associated Nascent DNA Method
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Published on: May 2, 2025

482

科学领域:

  • 分子生物学分子生物学
  • 生物物理学的生物物理.
  • 基因组学就是基因组学.

背景情况:

  • 单链DNA结合蛋白 (SSBs) 对于在复制过程中保护暴露的单链DNA (ssDNA) 至关重要.
  • 通过DNA聚合酶 (DNAp) 取代SSB以促进复制的机制尚未完全理解.

研究的目的:

  • 调查SSB在复制过程中被DNAp所取代的分子机制.
  • 为了阐明DNAp和SSB之间的时空协调.

主要方法:

  • 单分子力光谱学 单分子力光谱学
  • 双色图像成像技术的使用.
  • 分子动力学模拟的模拟.
  • 佛斯特共振能量转移 (FRET) 进行.

主要成果:

  • T7 SSB对复制的影响依赖于力,在低张力时增强,在高张力时阻碍.
  • 随着DNAp的进步,SSB保持静止,支持一个顺序移位模型.
  • DNAp通过与SSB C端尾的相互作用,积极降低SSB解离能量屏障.

结论:

  • DNAp和SSB之间的时空协调对于在复制过程中解决分子碰撞至关重要.
  • 这种协调确保了DNA复制过程性和基因组完整性.
  • 在SSB保护和复制效率之间的平衡对于最佳的DNA合成至关重要.