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相关概念视频

Nucleosome Remodeling02:54

Nucleosome Remodeling

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...
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...
The Replisome03:01

The Replisome

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 the...

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相关实验视频

Updated: Jul 7, 2026

Single-molecule Manipulation of G-quadruplexes by Magnetic Tweezers
08:28

Single-molecule Manipulation of G-quadruplexes by Magnetic Tweezers

Published on: September 19, 2017

机械地操纵DNA线程的合速率.

Thayaparan Paramanathan1, Fredrik Westerlund, Micah J McCauley

  • 1Department of Physics, Northeastern University, Boston, Massachusetts 02115, USA.

Journal of the American Chemical Society
|March 4, 2008
PubMed
概括
此摘要是机器生成的。

复合体Delta-Delta-P需要融化DNA来结合. 对DNA施加力以机械方式降低了这种融屏障,使结合速度更快,并揭示了线只需要一个基对融.

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Parallel High Throughput Single Molecule Kinetic Assay for Site-Specific DNA Cleavage
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Parallel High Throughput Single Molecule Kinetic Assay for Site-Specific DNA Cleavage

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Design and Synthesis of a Reconfigurable DNA Accordion Rack
07:44

Design and Synthesis of a Reconfigurable DNA Accordion Rack

Published on: August 15, 2018

相关实验视频

Last Updated: Jul 7, 2026

Single-molecule Manipulation of G-quadruplexes by Magnetic Tweezers
08:28

Single-molecule Manipulation of G-quadruplexes by Magnetic Tweezers

Published on: September 19, 2017

Parallel High Throughput Single Molecule Kinetic Assay for Site-Specific DNA Cleavage
06:51

Parallel High Throughput Single Molecule Kinetic Assay for Site-Specific DNA Cleavage

Published on: May 6, 2020

Design and Synthesis of a Reconfigurable DNA Accordion Rack
07:44

Design and Synthesis of a Reconfigurable DNA Accordion Rack

Published on: August 15, 2018

科学领域:

  • 生物物理学的生物物理.
  • 化学生物学 化学生物学
  • 分子生物物理学 分子生物物理学

背景情况:

  • 鲁复合体被研究为DNA插曲.
  • 融化DNA是连接像DeltaDelta-P这样的连接体的先决条件.
  • 由于罕见的DNA化事件,在批量实验中观察到较低的结合率.

研究的目的:

  • 为了研究机械操纵DNA化的障碍.
  • 通过DeltaDelta-P.P.来确定DNA线程的强力依赖.
  • 为了阐明用于连接体结合的最小DNA化要求.

主要方法:

  • 单个DNA分子伸展实验.
  • 对DNA施加受控的机械力.
  • 测量DeltaDelta-P在强力下与DNA的结合率.

主要成果:

  • 单个DNA分子的拉伸减少了DNA融化的障碍.
  • 德尔塔-德尔塔-P的DNA线程速率显示出对施加力的指数依赖.
  • 结合速率与机械力直接相关,与理论模型一致.

结论:

  • 机械力可以用来控制连接物与DNA的结合.
  • 只有一个暂时化的单个基对足以通过DeltaDelta-P进行DNA线程.
  • 这项研究提供了对DNA-配体相互作用和机械控制的见解.