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相关概念视频

Translesion DNA Polymerases02:10

Translesion DNA Polymerases

9.7K
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...
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The Replisome03:01

The Replisome

32.8K
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...
32.8K
Restarting Stalled Replication Forks02:37

Restarting Stalled Replication Forks

5.7K
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,...
5.7K
Homologous Recombination02:31

Homologous Recombination

50.0K
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...
50.0K
Radical Chain-Growth Polymerization: Overview01:10

Radical Chain-Growth Polymerization: Overview

2.3K
Chain-growth or addition polymerization is successive addition reactions of monomers with a polymer chain. In radical chain-growth polymerization, the reaction proceeds via a free-radical intermediate. The free radical is formed from radical initiators, which spontaneously generate free radicals by homolytic fission. Organic peroxides (such as dibenzoyl peroxide, as shown in Figure 1) or azo compounds are popular radical initiators. A low concentration ratio of radical initiator to monomer is...
2.3K
Single-Strand DNA Binding Proteins01:03

Single-Strand DNA Binding Proteins

13.9K
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...
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相关实验视频

Updated: May 24, 2025

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

Published on: April 4, 2025

315

通过使用聚四来加速托托介导的DNA链位移反应.

Junlan Liu1, Qing Zhang2

  • 1Department of Laboratory Medicine and Institute of Molecular Medicine (IMM), Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200240, China.

Chemistry (Weinheim an der Bergstrasse, Germany)
|March 5, 2025
PubMed
概括

聚四二 (PQ2) 极大地加快了托管介导链位移 (TMSD) 反应,使得DNA纳米技术应用具有低度的反应物. 这种简单,低成本的加速器提高了生物传感和分子计算的速度和可靠性.

关键词:
DNA 电路是 DNA 的电路.DNA纳米技术 DNA纳米技术分子动态系统分子动态系统聚四二是一种多方.拖拉力介导的拖丝移位.

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Plasmid-derived DNA Strand Displacement Gates for Implementing Chemical Reaction Networks
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Plasmid-derived DNA Strand Displacement Gates for Implementing Chemical Reaction Networks

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Real-time Observation of the DNA Strand Exchange Reaction Mediated by Rad51
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Real-time Observation of the DNA Strand Exchange Reaction Mediated by Rad51

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相关实验视频

Last Updated: May 24, 2025

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

Published on: April 4, 2025

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Plasmid-derived DNA Strand Displacement Gates for Implementing Chemical Reaction Networks
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Plasmid-derived DNA Strand Displacement Gates for Implementing Chemical Reaction Networks

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Real-time Observation of the DNA Strand Exchange Reaction Mediated by Rad51
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Real-time Observation of the DNA Strand Exchange Reaction Mediated by Rad51

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科学领域:

  • DNA纳米技术 DNA纳米技术
  • 分子生物学分子生物学
  • 生物化学 生物化学

背景情况:

  • 手持介导链位移 (TMSD) 是DNA纳米技术中的一个关键工具.
  • TMSD动力学往往很慢,特别是在低反应剂度的情况下,这限制了应用.

研究的目的:

  • 确定和评估TMSD反应的有效加速器.
  • 为了证明加速器在各种基于DNA的系统中的广泛适用性.

主要方法:

  • 研究了聚四二 (PQ2) 对TMSD反应动力学的影响.
  • 在基于TMSD的催化DNA放大器和多层电路中测试了PQ2.
  • 评估PQ2对反应速度,灵敏度和稳定性的影响.

主要成果:

  • PQ2将TMSD反应常数增加了105倍.
  • 在亚纳米和皮科莫尔输入方面实现了显著的加速.
  • 通过稳定DNA,增加局部度和减轻抑制因素,PQ2提高了性能.

结论:

  • PQ2是TMSD反应的高效和高效的加速器.
  • PQ2使得更快,更敏感,更强大的DNA纳米技术应用.
  • PQ2促进了生物传感和分子计算的先进应用.