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相关概念视频

Amplifying Signals via Enzymatic Cascade01:22

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When a ligand binds to a cell-surface receptor, the receptor's intracellular domain changes shape, which may either activate its enzyme function or allow its binding to other molecules. The initial signal is amplified by most signal transduction pathways. This means that a single ligand molecule can activate multiple molecules of a downstream target. Proteins that relay a signal are most commonly phosphorylated at one or more sites, activating or inactivating the protein. Kinases catalyze...
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Amplifying Signals via Second Messengers01:15

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Many receptor binding ligands are hydrophilic; they do not cross the cell membrane but bind to cell-surface receptors. Thus, their message must be relayed by second messengers present in the cell cytoplasm. There are several second messenger pathways, each with its own way of relaying information. For example, the G protein-coupled receptors can activate both phosphoinositol and cyclic AMP (cAMP) second messenger pathways. The phosphoinositol pathway is active when the receptor induces...
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Membrane lipids such as phosphatidylinositol (PI) are precursors for several membrane-bound and soluble second messengers. Specific kinases phosphorylate PI and produce phosphorylated inositol phospholipids. One such inositol phospholipids are the  phosphatidylinositol-4,5 bisphosphate [PI(4,5)P2], present in the inner half of the lipid bilayer. Upon ligand binding, GPCR stimulates Gq proteins to turn on phospholipase Cꞵ. Activated phospholipase Cꞵ cleaves PI(4,5)P2 and...
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Transducer Mechanism: Enzyme-Linked Receptors01:27

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Enzyme-linked receptors are cell-surface receptors acting as an enzyme or associating with an enzyme intracellularly. They make excellent drug targets. Drugs can bind to the extracellular ligand-binding domain or directly affect their enzymatic domain and alter their activity.
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Intracellular Signaling Cascades01:24

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Once a ligand binds to a receptor, the signal is transmitted through the membrane and into the cytoplasm. The continuation of a signal in this manner is called signal transduction. Signal transduction only occurs with cell-surface receptors, which cannot interact with most components of the cell, such as DNA. Only internal receptors can interact directly with DNA in the nucleus to initiate protein synthesis. When a ligand binds to its receptor, conformational changes occur that affect the...
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Signaling cascades usually lack linearity. Multiple pathways interact and regulate one another, allowing cells to integrate and respond to diverse environmental stimuli.
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Characterization at the Molecular Level using Robust Biochemical Approaches of a New Kinase Protein
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有关联体的分裂酶.

Karla Camacho-Soto1, Javier Castillo-Montoya, Blake Tye

  • 1Department of Chemistry and Biochemistry, University of Arizona , 1306 East University Boulevard, Tucson, Arizona 85721, United States.

Journal of the American Chemical Society
|February 19, 2014
PubMed
概括
此摘要是机器生成的。

研究人员设计了蛋白质激酶,以通过用户定义的输入来控制. 这种方法从不活跃的碎片中创建联结式分裂蛋白激酶,从而使分子生物学中的新应用成为可能.

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科学领域:

  • 生物化学 生物化学
  • 分子生物学分子生物学
  • 蛋白质工程是指蛋白质工程.

背景情况:

  • 蛋白激酶活性由自然的生理化学输入,如酸化和金属离子来调节.
  • 设计具有用户定义控制的合成蛋白激酶是生物技术中的一个重大挑战.

研究的目的:

  • 开发一种对响应用户定义输入的工程蛋白激酶的方法.
  • 为了创建具有保留催化活性的新型联结型分裂蛋白激酶.

主要方法:

  • 使用序列不相似性方法来确定适合在蛋白质激酶中插入25-残留环的位置.
  • 成功的循环插入突变分子引导了激酶的剖析成不活跃的碎片.
  • 碎片的重组是由联体结合触发的,以创建活跃的分裂蛋白激酶.

主要成果:

  • 在蛋白质激酶中确定了能够容忍循环插入的特定位点,同时保持催化功能.
  • 通过使用Lyn,Fak,Src和PKA,成功地证明了对联体门分裂蛋白激酶的工程.
  • 展示了开发方法在不同激酶家族的潜在普遍性.

结论:

  • 基于序列不相似性的方法对于设计可控制的蛋白激酶是有效的.
  • 这种方法可以创建对特定连接体有反应的催化活性分裂蛋白激酶.
  • 这些发现表明,它对于设计定制酶具有广泛的适用性.