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相关概念视频

Conserved Binding Sites01:49

Conserved Binding Sites

Many proteins’ biological role depends on their interactions with their ligands, small molecules that bind to specific locations on the protein known as ligand-binding sites. Ligand-binding sites are often conserved among homologous proteins as these sites are critical for protein function.
Binding sites are often located in large pockets, and if their location on a protein’s surface is unknown, it can be predicted using various approaches. The energetic method computationally analyses the...
Ligand Binding and Linkage00:49

Ligand Binding and Linkage

Allosteric proteins have more than one ligand binding site; the binding of a ligand to any of these sites influences the binding of ligands to the other sites. When a protein is allosteric, its binding sites are called coupled or linked.  In the case of enzymes, the site that binds to the substrate is known as the active site and the other site is known as the regulatory site. When a ligand binds to the regulatory site, this leads to conformational changes in the protein that can influence the...
Tagging and Fusion Proteins01:24

Tagging and Fusion Proteins

Proteins are involved in several cellular processes and biochemical reactions. Analyzing a specific protein of interest requires it to be isolated from the other proteins in the cell. This is achieved by overexpressing the specific gene in a suitable host to produce large quantities of the target protein. A tag or label is recombined with the gene to produce a fusion protein containing the target protein and the tag. The tags on these fusion proteins can then be used for easy detection and...

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相关实验视频

Updated: Jul 9, 2026

Membrane-SPINE: A Biochemical Tool to Identify Protein-protein Interactions of Membrane Proteins In Vivo
10:53

Membrane-SPINE: A Biochemical Tool to Identify Protein-protein Interactions of Membrane Proteins In Vivo

Published on: November 7, 2013

在蛋白激酶C中的结合位点的识别和表征.

S R Hubbard1, W R Bishop, P Kirschmeier

  • 1Howard Hughes Medical Institute, New York, NY.

Science (New York, N.Y.)
|December 20, 1991
PubMed
概括
此摘要是机器生成的。

蛋白激酶C (PKC) 紧密结合每分子的四个离子. 扩展的X射线吸收细结构 (EXAFS) 分析揭示了这些离子的一个和三个硫原子的协调.

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Detection of Heterodimerization of Protein Isoforms Using an in Situ Proximity Ligation Assay

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相关实验视频

Last Updated: Jul 9, 2026

Membrane-SPINE: A Biochemical Tool to Identify Protein-protein Interactions of Membrane Proteins In Vivo
10:53

Membrane-SPINE: A Biochemical Tool to Identify Protein-protein Interactions of Membrane Proteins In Vivo

Published on: November 7, 2013

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08:46

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Published on: September 16, 2014

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Detection of Heterodimerization of Protein Isoforms Using an in Situ Proximity Ligation Assay

Published on: October 20, 2018

科学领域:

  • 生物化学 生物化学
  • 结构生物学 结构生物学
  • 金属蛋白化学 金属蛋白化学

背景情况:

  • 蛋白激酶C (PKC) 在细胞信号通路中至关重要.
  • 在PKC的调节领域中保存的氨酸和氨酸残留物表明金属离子结合.
  • 金属离子在PKC中的精确作用和协调在很大程度上仍未被描述.

研究的目的:

  • 调查金属离子协调在蛋白激酶CβI (PKCβI) 的调节领域内的直接证据.
  • 为了确定PKCβ I. 中结合金属离子的固态度和协调环境.

主要方法:

  • 在昆虫细胞中过度表达大鼠PKCβI.
  • 净化PKCβ I. 的纯化.
  • 用X射线光光谱来监测金属离子结合.
  • 扩展的X射线吸收细结构 (EXAFS) 谱学以确定金属离子协调.

主要成果:

  • 发现PKCβI每分子紧密结合四个离子 (Zn2+).
  • EXAFS数据分析表明,一个和三个硫原子的平均Zn2+协调环境.
  • 可信的协调模型需要非桥接Zn2+站点来适应EXAFS数据和保存的连接体.

结论:

  • 直接证据证实离子与PKCβI结合.
  • 协调环境表明离子在PKC调节中的特定结构作用.
  • 这些发现提供了PKC功能结构基础的见解.