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Copper Binding Features of Tropomyosin-Receptor-Kinase-A Fragment: Clue for Neurotrophic Factors and Metals Link

机译:Tropomyosin-受体-激酶-A片段的铜结合特征:神经营养因子和金属链接的线索。

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摘要

The nerve growth factor (NGF) is a neurotrophin essential for the development and maintenance of neurons, whose activity is influenced by copper ions. The NGF protein exerts its action by binding to its specific receptor, TrkA. In this study, a specific domain of the TrkA receptor, region 58–64, was synthesized and its copper(II) complexes characterized by means of potentiometric and spectroscopic studies. The two vicinal histidine residues provide excellent metal anchoring sites and, at physiological pH, a complex with the involvement of the peptide backbone amide nitrogen is the predominant species. The TrkA peptide is competitive for metal binding with analogous peptides due to the N-terminal domain of NGF. These data provide cues for future exploration of the effect of metal ions on the activity of the NGF and its specific cellular receptor.
机译:神经生长因子(NGF)是神经营养素,对于神经元的发育和维持至关重要,其活性受铜离子的影响。 NGF蛋白通过结合其特异性受体TrkA发挥作用。在这项研究中,合成了TrkA受体的特定区域,区域58-64,并通过电位分析和光谱学研究表征了其铜(II)配合物。两个邻近的组氨酸残基提供了极好的金属锚定位点,并且在生理pH下,主要成分是与肽主链酰胺氮有关的复合物。由于NGF的N末端结构域,TrkA肽对于与类似肽的金属结合具有竞争性。这些数据为将来探索金属离子对NGF及其特异性细胞受体活性的影响提供了线索。

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