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相关概念视频

Lagging Strand Synthesis01:59

Lagging Strand Synthesis

54.0K
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...
54.0K
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

34.6K
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...
34.6K
Homologous Recombination02:31

Homologous Recombination

50.9K
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...
50.9K
DNA Replication02:40

DNA Replication

50.6K
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...
50.6K
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

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相关实验视频

Updated: Sep 5, 2025

Plasmid-derived DNA Strand Displacement Gates for Implementing Chemical Reaction Networks
07:50

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

Published on: November 25, 2015

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时间逻辑回路

Anna P Lapteva1, Namita Sarraf1, Lulu Qian1,2

  • 1Bioengineering, California Institute of Technology, Pasadena, California 91125, United States.

Journal of the American Chemical Society
|July 5, 2022
PubMed
概括
此摘要是机器生成的。

这项研究介绍了使用时间记忆和逻辑门来根据信号时间做出决定的DNA链位移电路. 这些电路可以进行复杂的分子计算,并为智能的人工分子机器铺平道路.

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Design and Synthesis of a Reconfigurable DNA Accordion Rack
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Design and Synthesis of a Reconfigurable DNA Accordion Rack

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DNA-Tethered RNA Polymerase for Programmable In vitro Transcription and Molecular Computation
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DNA-Tethered RNA Polymerase for Programmable In vitro Transcription and Molecular Computation

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相关实验视频

Last Updated: Sep 5, 2025

Plasmid-derived DNA Strand Displacement Gates for Implementing Chemical Reaction Networks
07:50

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

Published on: November 25, 2015

14.5K
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

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DNA-Tethered RNA Polymerase for Programmable In vitro Transcription and Molecular Computation
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DNA-Tethered RNA Polymerase for Programmable In vitro Transcription and Molecular Computation

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科学领域:

  • 合成生物学
  • 分子计算
  • 生物化学

背景情况:

  • 时间信息处理对于分子决策至关重要.
  • 相对信号定时是时间信息的一个关键方面.

研究的目的:

  • 展示用于时间逻辑计算的DNA链移位电路.
  • 根据输入组合和相对时间进行决策.

主要方法:

  • 使用内存链编码时间输入信息.
  • 设计处理当前和历史信号的逻辑门.
  • 使用不匹配和脚缩来优化电路.

主要成果:

  • 有时间记忆和逻辑能力的DNA电路的成功构建.
  • 通过不匹配证明了电路复杂性的降低.
  • 通过战略性脚修改提高了电路的稳定性.
  • 用于实验指导的详细建模的验证.

结论:

  • 在DNA电路中开发了时间记忆和逻辑计算的策略.
  • 设计原则可以用于复杂的时间逻辑和基于DNA的神经网络.
  • 这为人工分子机器的智能行为提供了机会.