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相关概念视频

Nuclear Protein Sorting01:34

Nuclear Protein Sorting

4.8K
Nuclear protein sorting is the selective trafficking of histones, polymerases, gene regulatory proteins into the nucleus and exporting RNAs and ribosomes to the cytosol. It is a tightly controlled process that regulates gene expression within a cell.
Proteins targeted to the nucleus carry nuclear localization signals or NLS recognized by import receptors in the cytosol. Similarly, proteins with nuclear export signals are recognized by export receptors. Import and export receptors are...
4.8K
Nuclear Localization Signals and Import01:46

Nuclear Localization Signals and Import

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Proteins targeted to the nucleus carry short stretches of amino acid sequences called the nuclear localization signal or NLS. Classical nuclear localization signals are of two types: monopartite and bipartite NLS. Monopartite classical NLS (cNLS) consists of a single cluster of 4-8 amino acids. Bipartite cNLS consists of two clusters of  2-3 amino acids and a 9-12 residue long proline-rich linker bridging the two clusters. Signal clusters are rich in positively charged amino acids such as...
6.2K
Nuclear Export01:42

Nuclear Export

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The nucleus restricts several proteins within and allows others to pass. The restricted proteins possess a nuclear retention sequence or NRS, anchoring them to the nuclear lamins and preventing their transport to the cytosol. The non-restricted proteins, after their synthesis, are transported to their site of action, such as the cytosol or other organelles, with the help of nuclear export signals or NES.
NES are of three types- the canonical 10-residue long leucine-rich signal and other...
3.7K
Directionality of Nuclear Transport01:42

Directionality of Nuclear Transport

3.9K
Ras-related nuclear protein or Ran is a small G protein that cycles between its GTP and GDP bound states. Ran specific regulators, a Ran GTPase Activating Protein or RanGAP present in the cytosol and a Ran guanine nucleotide exchange factor or RanGEF present inside the nucleus regulate GTP/GDP exchange. A high concentration of GTP inside the cells, in addition to this asymmetric distribution of  Ran-specific regulators, leads to a higher RanGTP concentration inside the nucleus. This...
3.9K
Rab Proteins01:14

Rab Proteins

4.0K
Rab proteins constitute the largest family of monomeric GTPases, of which 70 members are present in humans. Rab proteins and their effectors regulate consecutive stages of vesicle transport such as vesicle transport, docking, and fusion to the correct recipient membrane.
Rab proteins switch between a cytosolic, GDP-bound inactive state and a membrane-anchored, GTP-bound active state. By themselves, Rabs show slow rates of GDP/GTP exchange and GTP hydrolysis. Thus, Rab proteins are considered...
4.0K
RACE - Rapid Amplification of cDNA Ends02:35

RACE - Rapid Amplification of cDNA Ends

5.9K
Rapid Amplification of cDNA Ends, or RACE, is one of the most effective methods to obtain a full-length cDNA from an mRNA sequence between a known internal region to the unknown sequence at the 5’ or 3’ end. The unknown region is cloned in the cDNA by a gene-specific primer that binds the known end, and a hybrid primer that attaches a predefined anchor sequence to the unknown end of the cDNA. The sequence in between is amplified by PCR with an anchor primer and a gene-specific...
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相关实验视频

Updated: May 3, 2026

A Rapid High-throughput Method for Mapping Ribonucleoproteins RNPs on Human pre-mRNA
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A Rapid High-throughput Method for Mapping Ribonucleoproteins RNPs on Human pre-mRNA

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通过RanGTP进行核进口复合体解离的结构基础.

Soo Jae Lee1, Yoshiyuki Matsuura, Sai Man Liu

  • 1MRC Laboratory of Molecular Biology, Hills Rd, Cambridge CB2 2QH, UK.

Nature
|May 3, 2005
PubMed
概括
此摘要是机器生成的。

核蛋白进口依赖于进口蛋白-β和RanGTP. 绑定RanGTP到importin-beta会改变它的结构,释放货物并调节核运输.

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A Rapid High-throughput Method for Mapping Ribonucleoproteins RNPs on Human pre-mRNA
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A Rapid High-throughput Method for Mapping Ribonucleoproteins RNPs on Human pre-mRNA

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Isolation of Translating Ribosomes Containing Peptidyl-tRNAs for Functional and Structural Analyses
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科学领域:

  • 分子生物学分子生物学
  • 细胞生物学 细胞生物学
  • 结构生物学 结构生物学

背景情况:

  • 核蛋白进口对细胞功能至关重要.
  • 进口蛋白-β作为一个关键的运输因子,经常利用进口蛋白-α作为适配器.
  • 兰GTP驱动核中的进口复合体的分解.

研究的目的:

  • 阐明核进口综合体拆卸的结构基础.
  • 了解RanGTP从importin-beta释放货物的机制.

主要方法:

  • 使用X射线晶体学来确定酵母进口蛋白-β (Kap95p) 与RanGTP复合的结构.
  • 对复杂结构的分析,以确定关键的交互接口.

主要成果:

  • 确定了与RanGTP复合的全长酵母进口蛋白-β (Kap95p) 的结构.
  • 在RanGTP开关I循环和Kap95p的碳氧终端弧之间确定了一个关键的相互作用点.
  • 这种相互作用会诱导Kap95p的形状变化,防止货物结合.

结论:

  • 兰GTP与进口蛋白-β结合会导致一个全性形状变化.
  • 该机制解释了RanGTP如何在核进口过程中促进货物释放.
  • 这些发现为了解核运输法规提供了结构性基础.