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相关概念视频

Regulation of Nuclear Protein Sorting01:45

Regulation of Nuclear Protein Sorting

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Nuclear protein sorting regulates nucleus composition and gene expression, crucial for determining the fate of a eukaryotic cell. Hence, the entry and exit of molecules across the nuclear envelope is a tightly controlled process. Nuclear protein sorting can be inhibited by one of the following ways: 1) masking cargo signal sequences, 2) modifying the nuclear receptor's affinity for cargo, 3) controlling the nuclear pore size, 4) retaining the cargo during its transit to the cytosol or the...
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Nuclear Export of mRNA02:31

Nuclear Export of mRNA

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Before mRNAs are exported to the cytoplasm, it is crucial to check each mRNA for structural and functional integrity. Eukaryotic cells use several different mechanisms, collectively known as mRNA surveillance, to look for irregularities in mRNAs. Irregular or aberrant mRNA are rapidly degraded by various enzymes. If a defective mRNA escapes the surveillance, it would be translated into a protein which would either be non-functional or not function properly. One of the primary irregularities in...
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Nonsense-mediated mRNA Decay02:27

Nonsense-mediated mRNA Decay

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The Upf proteins that carry out nonsense-mediated decay (NMD) are found in all eukaryotic organisms, including humans. Each protein has an individual role, but they need to work in collaboration. Upf1 is an ATP-dependent RNA helicase that unwinds the RNA helix. Because Upf1 can unwind any RNA, Upf2 and Upf3 are required to help Upf1 discriminate between nonsense and normal mRNAs.
Usually, Upf3 binds to an Exon Junction Complex (EJC) at mRNA splice sites. If a ribosome fully translates the mRNA,...
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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...
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Nuclear Protein Sorting01:34

Nuclear Protein Sorting

4.9K
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...
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Export of Misfolded Proteins out of the ER01:32

Export of Misfolded Proteins out of the ER

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After folding, the ER assesses the quality of secretory and membrane proteins. The correctly folded proteins are cleared by the calnexin cycle for transport to their final destination, while misfolded proteins are held back in the ER lumen. The ER chaperones attempt to unfold and refold the misfolded proteins but sometimes fail to achieve the correct native conformation. Such terminally misfolded proteins are then exported to the cytosol by ER-associated degradation or ERAD pathway for...
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相关实验视频

Updated: Sep 29, 2025

Assays for the Degradation of Misfolded Proteins in Cells
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劫持用于核特异性蛋白质降解的甲基读取蛋白

Dhanusha A Nalawansha1, Ke Li1, John Hines1

  • 1Department of Molecular, Cellular and Developmental Biology, Yale University, New Haven, Connecticut 06511, United States.

Journal of the American Chemical Society
|March 21, 2022
PubMed
概括

研究人员通过劫持甲基阅读器-E3结合酶复合体,扩大向蛋白质降解工具,开发了新的PROTAC. 这种方法可以使FKBP12和BRD2等标蛋白进行核特异性降解.

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科学领域:

  • 生物化学
  • 分子生物学
  • 药物发现

背景情况:

  • 使用蛋白质分解向基因组 (PROTACs) 的向蛋白质降解 (TPD) 是控制疾病相关蛋白质的关键策略.
  • 目前的TPD工具箱因可用的E3酶:带对的稀缺性而受到限制.

研究的目的:

  • 通过使用甲基阅读器:E3结合酶复合物来诱导蛋白质降解的新方法.
  • 设计和评估用于向蛋白质降解的L3MBTL3甲基阅读器:E3结合酶复合物.

主要方法:

  • 设计和合成的PROTAC将L3MBTL3甲基阅读器招募到Cul4DCAF5 E3酶复合体中.
  • 评估了新型PROTACs在诱导核特异性蛋白质降解方面的生物活性.

主要成果:

  • 成功设计和验证了利用L3MBTL3:Cul4DCAF5复合体的PROTAC.
  • 使用新型PROTAC证明了蛋白FKBP12和BRD2的核特异性降解.

结论:

  • 绑架与甲基读者相关的E3酶复合体为PROTAC开发提供了一个可通用的策略来扩大E3酶谱.
  • 这种方法在药物发现中扩大了向蛋白质降解的潜力.