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Environmental Control of Amyloid Polymorphism by Modulation of Hydrodynamic Stress

机译:用水动力应力调节淀粉样蛋白多态性的环境控制

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The phenomenon of amyloid polymorphism is a key feature of protein aggregation. Unravelling this phenomenon is of great significance for understanding the underlying molecular mechanisms associated with neurodegenerative diseases and for the development of amyloid-based functional biomaterials. However, the understanding of the molecular origins and the physicochemical factors modulating amyloid polymorphs remains challenging. Herein, we demonstrate an association between amyloid polymorphism and environmental stress in solution, induced by an air/water interface in motion. Our results reveal that low-stress environments produce heterogeneous amyloid polymorphs, including twisted, helical, and rod-like fibrils, whereas high-stress conditions generate only homogeneous rod-like fibrils. Moreover, high environmental stress converts twisted fibrils into rodlike fibrils both in-pathway and after the completion of mature amyloid formation. These results enrich our understanding of the environmental origin of polymorphism of pathological amyloids and shed light on the potential of environmentally controlled fabrication of homogeneous amyloid biomaterials for biotechnological applications.
机译:淀粉样蛋白多态性现象是蛋白质聚集的一个关键特征。揭示这一现象对于理解与神经退行性疾病相关的潜在分子机制以及基于淀粉样蛋白的功能性生物材料的开发具有重要意义。然而,对调节淀粉样多晶型的分子起源和物理化学因素的理解仍然具有挑战性。在此,我们证明了淀粉样蛋白多态性与溶液中环境应激之间的关联,环境应激是由运动中的空气/水界面引起的。我们的研究结果表明,低应力环境会产生不均匀的淀粉样多晶型物,包括扭曲的、螺旋的和棒状的纤维,而高应力环境只会产生均匀的棒状纤维。此外,在成熟淀粉样蛋白形成的途径和完成后,高环境应力将扭曲的原纤维转化为棒状原纤维。这些结果丰富了我们对病理性淀粉样蛋白多态性的环境起源的理解,并揭示了环境控制制备同质淀粉样生物材料用于生物技术应用的潜力。

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