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相关概念视频

DNA Replication02:40

DNA Replication

48.1K
DNA replication involves the separation of the two strands of the double helix, with each strand serving as a template from which the new complementary strand is copied.  After replication, each double-stranded DNA includes one parental or “old” strand and one “new” strand. This is known as semiconservative replication. The resulting DNA molecules have the same sequence and are divided equally into the two daughter cells.
Replication in Prokaryotes
DNA replication...
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Lagging Strand Synthesis01:59

Lagging Strand Synthesis

48.8K
During replication, the complementary strands in double-stranded DNA are synthesized at different rates. Replication first begins on the leading strand. Replication starts later, occurs more slowly, and proceeds discontinuously on the lagging strand.
There are several major differences between synthesis of the leading strand and synthesis of the lagging strand. 1) Leading strand synthesis happens in the direction of replication fork opening, whereas lagging strand synthesis happens in the...
48.8K
The Replisome03:01

The Replisome

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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...
32.7K
The DNA Replication Fork01:02

The DNA Replication Fork

35.3K
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...
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Replication in Eukaryotes02:31

Replication in Eukaryotes

170.0K
Overview
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DNA as a Genetic Template02:05

DNA as a Genetic Template

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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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相关实验视频

Updated: May 17, 2025

DNA Origami-Mediated Substrate Nanopatterning of Inorganic Structures for Sensing Applications
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DNA Origami-Mediated Substrate Nanopatterning of Inorganic Structures for Sensing Applications

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托波加米:链接DNA原始体

Gerrit Wilkens1, Piotr Stepien2, Ahmed Shaukat2

  • 1Université de Montpellier, Centre de Biochimie Structurale, CNRS, INSERM, Montpellier, France.

Methods in molecular biology (Clifton, N.J.)
|April 2, 2025
PubMed
概括

通过使用溶解酶酶连接它们的脚手架链,DNA拓木法使DNA原木结构的稳定连接成为可能. 这种技术允许从多个DNA原始体单元中创建更大,更复杂的纳米级机器.

关键词:
在DNA中,有连锁的DNA.基因原始的DNA原始化一个DNA环,一个DNA环.在Tn3解决方案中.

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Folding and Characterization of a Bio-responsive Robot from DNA Origami
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Folding and Characterization of a Bio-responsive Robot from DNA Origami

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Designing a Bio-responsive Robot from DNA Origami
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Designing a Bio-responsive Robot from DNA Origami

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相关实验视频

Last Updated: May 17, 2025

DNA Origami-Mediated Substrate Nanopatterning of Inorganic Structures for Sensing Applications
08:59

DNA Origami-Mediated Substrate Nanopatterning of Inorganic Structures for Sensing Applications

Published on: September 27, 2019

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Folding and Characterization of a Bio-responsive Robot from DNA Origami
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科学领域:

  • 纳米技术 纳米技术
  • 分子生物学分子生物学
  • 生物技术是生物技术.

背景情况:

  • 基因原形是构建纳米级机器的通用方法.
  • 在个别DNA原始结构的尺寸上存在限制.
  • 对于更大的功能构造,结合多个DNA原始体单位是必要的.

研究的目的:

  • 介绍DNA拓波加米方法,用于链接DNA原始结构.
  • 为了实现更大,更稳定的纳米级组件的创建.
  • 为了克服单个DNA原木单元的尺寸限制.

主要方法:

  • 在DNA拓波加米方法中,使用了溶解酶.
  • 基架链的DNA原木结构是连锁的.
  • 用主丝将连锁脚手架折叠成所需结构.

主要成果:

  • 通过连接DNA原木脚手架链来实现真正的连接.
  • 演示了多个DNA原木单元稳定链接的方法.
  • 能够形成更大,更整合的DNA原木结构.

结论:

  • 基因托波加米方法为DNA原始结构提供了稳定的链接.
  • 这种技术有助于构建复杂的,多个单元的纳米级机器.
  • DNA Topogami克服了DNA原木组装中以前的尺寸限制.