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CONCERTED ACTION OF METALS AND MACROMOLECULAR CROWDING ON THE FIBRILLATION OF α-SYNUCLEIN

机译:金属和大分子拥挤对α-突触核蛋白原纤化的协同作用

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摘要

Certain metals lead to increased risk of Parkinson’s disease (PD) and the aggregation of α-synuclein is implicated in the PD pathology. Although α-synuclein fibrillation has been extensively studied in dilute solutions in vitro, the intracellular environment is highly crowded. We are showing here that certain metals cause a significant acceleration of α-synuclein fibrillation in the presence of high concentrations of various macromolecules mostly through decreasing the fibrillation lagtime. The faster fibrillation in crowded environments in the presence of heavy metals suggests a simple molecular basis for the observed elevated risk of PD due to exposure to metals.
机译:某些金属会导致帕金森氏病(PD)的风险增加,并且PD病理学中涉及α-突触核蛋白的聚集。尽管已经在体外稀溶液中对α-突触核蛋白原纤维化进行了广泛研究,但细胞内环境高度拥挤。我们在这里表明,某些金属在高浓度的各种大分子存在下会导致α-突触核蛋白原纤化的明显加速,这主要是通过减少原纤化的滞后时间而实现的。在重金属存在的拥挤环境中,较快的原纤化表明,由于暴露于金属而导致PD风险升高的简单分子基础。

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