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相关概念视频

Mitochondrial Protein Sorting01:39

Mitochondrial Protein Sorting

5.8K
Mitochondria are double-membrane organelles of the eukaryotes involved in cellular metabolism, signaling, ATP synthesis, and programmed cell death.  Each of these processes requires specific proteins and enzymes that must be correctly sorted to the right mitochondrial subcompartment for the proper functioning of the organelle.
Most of these mitochondrial proteins are encoded by the nucleus and imported to the mitochondria as unfolded or loosely folded precursors. Mitochondrial precursors...
5.8K
Nuclear Protein Sorting01:34

Nuclear Protein Sorting

6.4K
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...
6.4K
Overview of Protein Sorting and Transport01:45

Overview of Protein Sorting and Transport

23.0K
Eukaryotic cells have different membrane-bound organelles with distinct protein requirements. The process by which proteins are targeted to a specific organelle is called protein sorting.
Protein sorting can be of two types: signal-based sorting and vesicle-based trafficking. In signal-based sorting, specific amino acid sequences called sorting signals target proteins to the proper location inside the cell either via gated transport or by protein translocation.  In gated transport, folded...
23.0K
Signal Sequences and Sorting Receptors01:41

Signal Sequences and Sorting Receptors

15.5K
Signal sequences are short amino acid sequences that guide newly synthesized proteins to their proper location within the cell. Classical signal sequences are fifteen to sixty amino acids long and present at the N-terminus of a polypeptide chain. Each signal sequence has a conserved segment of basic residues towards their N terminus, a hydrophobic core, and a C-terminus rich in polar residues. The C-terminus also contains a signal cleavage site and features a -3 -1 sequence motif. The -3-1...
15.5K
Regulation of Nuclear Protein Sorting01:45

Regulation of Nuclear Protein Sorting

3.4K
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...
3.4K
Protein Kinases and Phosphatases02:54

Protein Kinases and Phosphatases

15.2K
Proteins undergo chemical modifications that trigger changes in the charge, structure, and conformation of the proteins. Phosphorylation, acetylation, glycosylation, nitrosylation, ubiquitination, lipidation, methylation, and proteolysis are various protein modifications that regulate protein activity. Such modifications are usually enzyme-driven.
Protein kinases
Many proteins in the cell are regulated by phosphorylation, the addition of a phosphate group. A family of enzymes called kinases...
15.2K

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相关实验视频

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Identification of Kinase-substrate Pairs Using High Throughput Screening
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使用超级纳米反应器进行基板分类

Yusuke Azuma1, Daniel L V Bader1, Donald Hilvert1

  • 1Laboratory of Organic Chemistry, ETH Zurich , 8093 Zurich, Switzerland.

Journal of the American Chemical Society
|December 27, 2017
PubMed
概括
此摘要是机器生成的。

具有充电内部的工程蛋白质可以分类和降解特定的蛋白质基质. 这种纳米反应器技术增强了受控蛋白质降解的酶特异性.

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科学领域:

  • 生物化学
  • 分子生物学
  • 纳米技术

背景情况:

  • 细胞蛋白质降解依赖于空间时间控制的分离.
  • 工程蛋白质提供了在狭窄空间内控制酶活性的潜力.

研究的目的:

  • 调查使用超充电蛋白来控制蛋白酶基质的特异性.
  • 在纳米反应器中展示基板的静电分类.

主要方法:

  • 设计一个带负电荷的光酶蛋白.
  • 在工程子中封装一个蛋白酶.
  • 使用具有不同电荷的多来评估基质裂变偏好.

主要成果:

  • 有负电荷的纳米室优先降解有正电荷的多.
  • 封装蛋白质酶的基质特异性被反转了大约480倍.
  • 在子内的静电相互作用决定了基板的选择.

结论:

  • 超电纳米室可以赋予封装酶的基质特异性.
  • 这种方法提供了一种通过静电排序控制催化剂活性的一般方法.
  • 在向蛋白质降解和合成生物学中的潜在应用.