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相关概念视频

Conservative Site-specific Recombination and Phase Variation02:53

Conservative Site-specific Recombination and Phase Variation

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Because the DNA segments are cut and reorganized in a direction-specific manner, site-specific recombination has emerged as an efficient genetic engineering technique. Flippase and Cyclization recombinases or Flp and Cre, respectively, are two members of the tyrosine recombinase family derived from bacteriophages, that are used to mediate site-specific DNA insertions, deletions, and targeted expression of proteins in mammalian cell lines.
The recognition sites for Cre recombinase called LoxP...
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Homologous Recombination02:31

Homologous Recombination

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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...
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Restarting Stalled Replication Forks02:37

Restarting Stalled Replication Forks

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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,...
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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...
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Restriction Enzymes01:11

Restriction Enzymes

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Restriction enzymes are bacterial enzymes used to cut DNA in a sequence-specific manner. To cleave DNA, they bind to specific palindromic sequences called restriction sites. Such palindromic DNA sequences or inverted repeats are commonly found in regions of functional significance, such as the origin of replication, gene operator sites, and regions containing transcription termination signals.
The host bacteria protect their own genomic DNA from these enzymes by methylating these sites. Some...
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Translesion DNA Polymerases02:10

Translesion DNA Polymerases

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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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相关实验视频

Updated: Jul 8, 2025

Design and Synthesis of a Reconfigurable DNA Accordion Rack
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控制pH的可重置的模块化DNA链移位电路

Xiaoyun Sun1, Dongbao Yao1, Haojun Liang1

  • 1Hefei National Research Center for Physical Sciences at the Microscale, Department of Polymer Science and Engineering, School of Chemistry and Materials Science, Collaborative Innovation Center of Chemistry for Energy Materials (iChEM), University of Science and Technology of China, Hefei, Anhui 230026, China.

Nano letters
|December 12, 2023
PubMed
概括

研究人员开发了一种新的以质子驱动的方法来重置动态DNA电路. 这一策略使得DNA纳米技术系统的重复运行无需浪费,进步了分子计算和诊断.

关键词:
可拆卸的基板基板可以拆卸.这是我的动机.响应pH的分子间三倍体.可重置的模块化DNA电路通过杆介导的子移位.

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科学领域:

  • 分子纳米技术 分子纳米技术
  • 生物化学 生物化学
  • 合成生物学 合成生物学

背景情况:

  • 动态DNA纳米技术依赖于分子系统的脚介导链位移 (TMSD).
  • 由于反向反应动力学方面的挑战,现有的TMSD系统缺乏简单的重置机制.

研究的目的:

  • 开发一种简单有效的策略来重置基于TMSD的动态DNA电路.
  • 为了使模块化DNA电路在恒温下在不产生废物的情况下重复运行.

主要方法:

  • 将响应pH的分子间CG-C+三重DNA和i-动机DNA集成到DNA基质中.
  • 使用pH编程的策略来控制DNA组件的结合/解离.
  • 通过pH诱导的结构变化促进前向和后向TMSD反应.

主要成果:

  • 成功开发了一种以质子驱动的策略,用于完全重置模块化DNA电路.
  • 该系统证明了在恒温下重复运行而不会产生DNA废物.
  • 构建了用于计算的可重置DNA逻辑门和用于信号转导的催化DNA系统.

结论:

  • 开发的pH编程策略提供了一个可操作的方法来重置基于TMSD的动态DNA系统.
  • 这种方法提高了DNA纳米技术应用的可重复使用性和可持续性.
  • 构建的可重置逻辑门和催化系统显示了先进分子计算和诊断的前景.