Jove
Visualize
联系我们
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关概念视频

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...
Fixing Double-strand Breaks02:04

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...
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...
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...
Fixing Double-strand Breaks02:04

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...
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...

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

Sensitive detection of prostate cancer antigen 3 (PCA3) in urine based upon CRISPR/Cas12a and gold nanorods (AuNRs).

Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy·2026
Same author

How Spontaneous Electrowetting and Surface Charge Affect Drop Motion.

Physical review letters·2026
Same author

Bottom-up synthesis of molecular nanodiamond from nanographene.

Nature·2026
Same author

Self-amplifying cascade-triggered Au NP assembly strategy for ultrasensitive cTnI detection with dynamic light scattering.

Analytical methods : advancing methods and applications·2026
Same author

Fabrication of Janus Supraparticles by Induced Phase Separation by Gravity.

ACS nano·2026
Same author

Wetting of granular and porous materials.

Advances in colloid and interface science·2026

相关实验视频

Updated: Jul 7, 2026

Analyzing and Building Nucleic Acid Structures with 3DNA
16:24

Analyzing and Building Nucleic Acid Structures with 3DNA

Published on: April 26, 2013

在三重DNA中,第三个链和双链之间的断裂力是三重DNA中的断裂力.

Liansheng Ling1, Hans-Jürgen Butt, Rüdiger Berger

  • 1Max-Planck Institute for Polymer Research, Mainz 55128, Germany.

Journal of the American Chemical Society
|October 28, 2004
PubMed
概括

原子力光谱测量了三重DNA的破裂力. 将第三个链与双重DNA分离需要42.6 ± 1.9 pN,这表明发生了热解离过程.

科学领域:

  • 分子生物学分子生物学
  • 生物物理学的生物物理.
  • 纳米技术纳米技术

背景情况:

  • DNA可以形成超出规范双螺旋的复杂结构.
  • 三重DNA,涉及三个链,呈现独特的结构和功能性质.
  • 了解DNA结构的机械稳定性对于分子工程和生物见解至关重要.

研究的目的:

  • 在三重结构中,量化将第三个链从双重DNA分离所需的破裂力.
  • 通过原子力光谱学研究DNA三重组的机械性质和稳定性.
  • 为了探索DNA三重复的热解离过程.

主要方法:

  • 原子力显微镜 (AFM) 尖端和样品表面的功能化与特定的寡氧化核酸.
  • 在特定的pH值和离子条件下,样品表面形成DNA复合体,随后形成三重复合体.
  • 使用AFM力-距离曲线测量破裂力,并分析破裂力直方图.

主要成果:

  • 对单个和多个三重DNA破裂事件观察到不同的信号.
  • 确定了42.6±1.9 pN的破裂力,以400 nm/s的尖端速度将第三个链从双重DNA分离出来.
  • 证明破裂力表现出速度依赖,这是热解离过程的特征.

更多相关视频

Capturing Chromosome Conformation Across Length Scales
10:15

Capturing Chromosome Conformation Across Length Scales

Published on: January 20, 2023

Capturing Common Fragile Site Breaks by Native γH2A.X ChIP
09:46

Capturing Common Fragile Site Breaks by Native γH2A.X ChIP

Published on: January 24, 2025

相关实验视频

Last Updated: Jul 7, 2026

Analyzing and Building Nucleic Acid Structures with 3DNA
16:24

Analyzing and Building Nucleic Acid Structures with 3DNA

Published on: April 26, 2013

Capturing Chromosome Conformation Across Length Scales
10:15

Capturing Chromosome Conformation Across Length Scales

Published on: January 20, 2023

Capturing Common Fragile Site Breaks by Native γH2A.X ChIP
09:46

Capturing Common Fragile Site Breaks by Native γH2A.X ChIP

Published on: January 24, 2025

结论:

  • 用AFM可以准确地测量DNA三重链的机械稳定性.
  • 三重DNA的破裂力与双链DNA的破裂力相当,这表明类似的解离机制.
  • 三重DNA的形成和破裂可以通过调整寡核酸度来控制,这为分子操纵提供了潜力.