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相关概念视频

PCR01:32

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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.
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In the same year as the discovery of the Sanger sequencing method, another group of scientists, Allan Maxam and Walter Gilbert, demonstrated their chemical-cleavage method for DNA sequencing. The Maxam-Gilbert method relies on using different chemicals that can cleave the DNA sequence at specific sites, the separation of resulting DNA fragments of variable size using electrophoresis, and deciphering the DNA sequence from the resulting gel bands.
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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.
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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.
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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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Rapid, Enzymatic Methods for Amplification of Minimal, Linear Templates for Protein Prototyping using Cell-Free Systems
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使用通用模板进行多步DNA模板合成.

Yizhou Li1, Peng Zhao, Mingda Zhang

  • 1Key Laboratory of Bioorganic Chemistry and Molecular Engineering of the Ministry of Education, Beijing National Laboratory of Molecular Sciences (BNLMS), College of Chemistry and Molecular Engineering, Peking University , 202 Chengfu Road, Beijing, China 100871.

Journal of the American Chemical Society
|November 16, 2013
PubMed
概括
此摘要是机器生成的。

一种新的DNA模板合成方法使用通用DNA模板来构建各种DNA编码库. 这种方法简化了库合成,目标选择和击中解码,用于更广泛的化学应用.

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科学领域:

  • 化学生物学 化学生物学
  • 分子生物学分子生物学
  • 合成化学 合成化学

背景情况:

  • DNA编码图书馆 (DEL) 为药物发现提供了一个强大的平台.
  • 目前的DEL合成方法可能很复杂,需要多个DNA模板.

研究的目的:

  • 开发一种精简的DNA模板合成方法,用于创建多样化的DNA编码库.
  • 为了证明一种新的"通用模板"对于有效的图书馆构建和分析的实用性.

主要方法:

  • 一个单一的DNA模板,包括deoxyinosine被设计为不分青红白的基础配对.
  • 可光分裂的链接器和由反应DNA直接编码被集成到系统中.
  • 该通用模板被用于库合成,目标选择和击中解码.

主要成果:

  • 通过使用单一的通用DNA模板,成功构建了一个完整的DNA编码库.
  • 证明了指导多种化学反应的效率,具有多种不同的反应物DNA.
  • 在库合成,目标选择和击中解码方面验证了功能.

结论:

  • 通用模板方法为准备各种DNA编码库提供了通用和简单的方法.
  • 这种技术简化了DEL合成,使其在化学生物学和药物发现中具有更广泛的应用.