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関連する概念動画

DNA Helicases00:55

DNA Helicases

DNA unwinding helicase enzymes are a type of motor protein. Motor proteins can translocate along filaments or polymers using energy generated from ATP hydrolysis. Helicases are involved in all the important cellular processes where DNA unwinding is required, such as DNA replication, repair, recombination, and transcription. They are present in all living organisms, but vary in their structure, function, and mechanism of action. For example, in prokaryotes, DnaB helicase binds and translocates...
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...
Overview of DNA Repair02:25

Overview of DNA Repair

In order to be passed through generations, genomic DNA must be undamaged and error-free. However, every day, DNA in a cell undergoes several thousand to a million damaging events by natural causes and external factors. Ionizing radiation such as UV rays, free radicals produced during cellular respiration, and hydrolytic damage from metabolic reactions can alter the structure of DNA. Damages caused include single-base alteration, base dimerization, chain breaks, and cross-linkage.
Chemically...
Single-Strand DNA Binding Proteins01:03

Single-Strand DNA Binding Proteins

For successful DNA replication, the unwinding of double-stranded DNA must be accompanied by stabilization and protection of the separated single strands of the DNA. This crucial task is performed by single-strand DNA-binding (SSB) proteins. They bind to the DNA in a sequence-independent manner, which means that the nitrogenous bases of the DNA need not be present in a specific order for binding of SSB proteins to it. The binding of SSB proteins straightens single-stranded DNA (ssDNA) and makes...
Homologous Recombination02:31

Homologous Recombination

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...
DNA Bacteriophages01:26

DNA Bacteriophages

Bacteriophages, or phages, are viruses that specifically infect bacteria, utilizing their genetic material to hijack host cellular machinery for replication. DNA bacteriophages employ single-stranded DNA (ssDNA) or double-stranded DNA (dsDNA) genomes. These phages exhibit diverse replication strategies and host interactions, influencing their ecological roles and applications in biotechnology and medicine.ssDNA BacteriophagesssDNA phages, with their small genomes, utilize unique strategies to...

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関連する実験動画

Updated: May 11, 2026

DNAzyme 10-23 - Based Nanomachines for Nucleic Acid Recognition
07:16

DNAzyme 10-23 - Based Nanomachines for Nucleic Acid Recognition

Published on: February 9, 2024

DNAを水分解する小さな,非常に活発なDNAです.

Hongzhou Gu1, Kazuhiro Furukawa, Zasha Weinberg

  • 1Department of Molecular, Cellular and Developmental Biology, Yale University, New Haven, Connecticut 06520, USA.

Journal of the American Chemical Society
|May 18, 2013
PubMed
まとめ

科学者たちは,DNAを急速に分解するデオキシリボジームを設計しました. これらのDNA切断酵素は,亜鉛イオンで中性に近いpHで活性化しており,天然のDNA配列からのゲノム不安定性の潜在的なリスクを強調しています.

科学分野:

  • バイオケミストリー バイオケミストリー
  • 分子生物学は分子生物学である.
  • 遺伝学 遺伝学とは

背景:

  • DNAのフォスフォースター結合は,触媒なしで水解に高い耐性を示します.
  • この安定性は,大型のゲノムで長期にわたる遺伝情報保存に不可欠です.
  • ゲノム不安定は,意図しないDNAの劣化から生じる可能性があります.

研究 の 目的:

  • 選択的かつ迅速なDNA水解を可能にする新しいデオキシリボジームを設計する.
  • エンジニアリングによるデオキシリボジームの触媒効率と特性を分析する.
  • 自然なDNA配列が自己水解を起こす可能性を調査する.

主な方法:

  • デオキシリボ酵素の2つのクラスの設計と合成.
  • 観察された速度定数 (k ((obs)) を含む,触媒活動の特徴.
  • 特定の条件下でデオキシリボ酵素のインキュベーション (中性に近いpH,Zn(2+の存在)).
  • 触媒条件下での自然DNA配列の選択と分析.

主要な成果:

  • エンジニアリングクラスIデオキシリボ酵素は,約1分〜"分の観測速度常数 (k ((obs)) を達成しました.

さらに関連する動画

Using Modified Synthetic Oligonucleotides to Assay Nucleic Acid-Metabolizing Enzymes
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Using Modified Synthetic Oligonucleotides to Assay Nucleic Acid-Metabolizing Enzymes

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DNAzyme-dependent Analysis of rRNA 2’-O-Methylation
09:12

DNAzyme-dependent Analysis of rRNA 2’-O-Methylation

Published on: September 16, 2019

関連する実験動画

Last Updated: May 11, 2026

DNAzyme 10-23 - Based Nanomachines for Nucleic Acid Recognition
07:16

DNAzyme 10-23 - Based Nanomachines for Nucleic Acid Recognition

Published on: February 9, 2024

Using Modified Synthetic Oligonucleotides to Assay Nucleic Acid-Metabolizing Enzymes
05:33

Using Modified Synthetic Oligonucleotides to Assay Nucleic Acid-Metabolizing Enzymes

Published on: July 5, 2024

DNAzyme-dependent Analysis of rRNA 2’-O-Methylation
09:12

DNAzyme-dependent Analysis of rRNA 2’-O-Methylation

Published on: September 16, 2019

  • 触媒作用は,亜鉛イオン (Zn(2+)) の存在で中性pHの近くで観察されました.
  • コンセンサスクラスIの構造を持つ自然DNA配列は,選択条件下 (2 mM Zn(2+),pH 7) で水分解することが判明しました.
  • 結論:

    • エンジニアリングされたデオキシリボ酵素は,効率的なDNA水解を証明しています.
    • この発見は,特定のDNA配列構造には,固有の触媒特性がある可能性があることを示唆している.
    • この固有の触媒的潜在力は,ゲノム不安定に寄与する可能性があります.