Zhou Jiangtao, Venturelli Leonardo, Keiser Ludovic, Sekatskii Sergey K, Gallaire François, Kasas Sandor, Longo Giovanni, Knowles Tuomas P J, Ruggeri Francesco S, Dietler Giovanni
Laboratory of Physics of Living Matter, École Polytechnique Fédérale de Lausanne (EPFL), CH-1015 Lausanne, Switzerland.
Laboratory of Fluid Mechanics and Instabilities, École Polytechnique Fédérale de Lausanne (EPFL), CH-1015 Lausanne, Switzerland.
ACS Nano. 2021 Jan 26;15(1):944-953. doi: 10.1021/acsnano.0c07570. Epub 2020 Dec 22.
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 rod-like 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.
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,对淀粉样蛋白多态体的分子起源和调节其形成的物理化学因素的理解仍然具有挑战性。在此,我们证明了溶液中的淀粉样蛋白多态性与由运动的空气/水界面诱导的环境应力之间的关联。我们的结果表明,低应力环境会产生异质的淀粉样蛋白多态体,包括扭曲的、螺旋状的和棒状的纤维,而高应力条件下仅产生均匀的棒状纤维。此外,高环境应力会在成熟淀粉样蛋白形成过程中和形成后将扭曲的纤维转化为棒状纤维。这些结果丰富了我们对病理性淀粉样蛋白多态性环境起源的理解,并为环境可控制备用于生物技术应用的均匀淀粉样蛋白生物材料的潜力提供了启示。