Institute of Biostructures and Bioimages, National Council of Research (CNR), Via Paolo Gaifami 18, 95126 Catania, Italy.
Consorzio Interuniversitario di Ricerca in Chimica dei Metalli nei Sistemi Biologici (CIRCMSB), via Celso Ulpiani, 27, 70125 Bari, Italy.
Int J Mol Sci. 2018 Aug 12;19(8):2374. doi: 10.3390/ijms19082374.
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.
神经生长因子(NGF)是一种对神经元的发育和维持至关重要的神经营养因子,其活性受铜离子的影响。NGF 蛋白通过与其特定受体 TrkA 结合发挥作用。在这项研究中,合成了 TrkA 受体的一个特定结构域,即 58-64 区,并通过电位和光谱研究对其铜(II)配合物进行了表征。两个相邻的组氨酸残基提供了极好的金属固定位点,在生理 pH 值下,与肽骨架酰胺氮参与的配合物是主要物种。由于 NGF 的 N 端结构域,TrkA 肽与类似肽竞争金属结合。这些数据为未来探索金属离子对 NGF 及其特定细胞受体活性的影响提供了线索。