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相关概念视频

Long-patch Base Excision Repair01:02

Long-patch Base Excision Repair

Since the discovery of the two BER pathways, there has been a debate about how a cell chooses one pathway over the other and the factors determining this selection. Numerous in vitro experiments have pointed out multiple determinants for the sub-pathway selection. These are:
Gene Conversion02:08

Gene Conversion

Other than maintaining genome stability via DNA repair, homologous recombination plays an important role in diversifying the genome. In fact, the recombination of sequences forms the molecular basis of genomic evolution. Random and non-random permutations of genomic sequences create a library of new amalgamated sequences. These newly formed genomes can determine the fitness and survival of cells. In bacteria, homologous and non-homologous types of recombination lead to the evolution of new...
Overview of Transposition and Recombination02:13

Overview of Transposition and Recombination

Transposons make up a significant part of genomes of various organisms. Therefore, it is believed that transposition played a major evolutionary role in speciation by changing genome sizes and modifying gene expression patterns. For example, in bacteria, transposition can lead to conferring antibiotic resistance. Movement of transposable elements within the genetic pool of pathogenic bacteria can aid in transfer of antibiotic-resistant genetic elements. In eukaryotes, transposons can carry out...
DNA-only Transposons02:57

DNA-only Transposons

DNA-only transposons are called autonomous transposons since they code for the enzyme transposase that is required for the transposition mechanism. Insertion of transposons can alter gene functions in multiple ways. They can mutate the gene, alter gene expression by introducing a novel promoter or insulator sequence, introduce new splice sites, and change the mRNA transcripts produced, or remodel chromatin structure.
The donor site from where the transposon is excised is either degraded or...
piRNA - Piwi-interacting RNAs02:57

piRNA - Piwi-interacting RNAs

PIWI-interacting RNAs, or piRNAs, are the most abundant short non-coding RNAs. More than 20,000 genes have been found in humans that code for piRNAs while only 2000 genes have been found for miRNAs. piRNAs can act at the transcriptional and post-transcriptional levels and have a vital role in silencing transposable elements present in germ cells. They are also involved in epigenetic silencing and activation. Previously, they were thought to function only in germ cells but new evidence suggests...
Insensitive Nuclei Enhanced by Polarization Transfer (INEPT)01:15

Insensitive Nuclei Enhanced by Polarization Transfer (INEPT)

Insensitive Nuclei Enhanced by Polarization Transfer (INEPT) is an advanced Nuclear Magnetic Resonance (NMR) technique specifically designed to detect and enhance the signals of low-abundance nuclei, such as carbon-13 and nitrogen-15, in small molecules. The fundamental principle behind INEPT is the transfer of polarization from a more abundant and highly polarizable nucleus, typically hydrogen-1, to the low-abundance nucleus of interest. This process effectively boosts the NMR signal of the...

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相关实验视频

Updated: Jul 6, 2026

Sequence-specific and Selective Recognition of Double-stranded RNAs over Single-stranded RNAs by Chemically Modified Peptide Nucleic Acids
09:04

Sequence-specific and Selective Recognition of Double-stranded RNAs over Single-stranded RNAs by Chemically Modified Peptide Nucleic Acids

Published on: September 21, 2017

在 PNA:DNA 杂交体中,高效的跨链过剩电子转移.

Michaela K Cichon1, Clemens H Haas, Friederike Grolle

  • 1Department of Chemistry, Philipps-University Marburg, D-35032 Marburg, Germany.

Journal of the American Chemical Society
|November 21, 2002
PubMed
概括

通过核酸 (PNA) 过量的电子转移:DNA基在链之间是高效的. 这项研究探讨了距离,序列和堆叠如何影响这种电子转移过程.

科学领域:

  • 超分子化学 超分子化学
  • 生物物理化学 生物物理化学
  • 分子电子学分子电子学

背景情况:

  • 核酸 (PNA) 是DNA模仿物,在分子电子学中具有潜在的应用.
  • 了解PNA:DNA混合体中的电荷传输对于开发新型电子设备至关重要.

研究的目的:

  • 为了研究通过PNA:DNA基过量电子转移的效率.
  • 探索距离,序列和堆叠对电链间电子转移的影响.

主要方法:

  • 合成PNA:DNA链,其中包含一个flavin电子捐赠体和一个thymine二元接受体.
  • 使用构造来诱导在单个电子减少时的链断裂.

主要成果:

  • 通过基层堆确认了有效的跨链过剩电子转移.
  • 证明增加距离,改变序列和堆叠显著影响传输效率.

结论:

  • 在PNA:DNA混合体中,过量的电子转移是可行的和可控的.
  • 这些发现为设计基于核酸结构的分子电子元件提供了洞察力.

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