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金属离子可以调节催化肽淀粉样纤维的自组装和活性。

Metal Ions Can Modulate the Self-Assembly and Activity of Catalytic Peptide Amyloids.

机构信息

Departamento de Biología, Facultad de Química y Biología, Universidad de Santiago de Chile, General Amengual 014, Estación Central, Santiago 9170390, Chile.

Departamento de Biología, Facultad de Ciencias, Universidad de Chile, Las Palmeras 3425, Ñuñoa, Santiago 7800003, Chile.

出版信息

Langmuir. 2024 Mar 26;40(12):6094-6106. doi: 10.1021/acs.langmuir.3c02983. Epub 2024 Mar 12.

DOI:10.1021/acs.langmuir.3c02983
PMID:38470353
Abstract

Rational design of peptides has become a powerful tool to produce self-assembled nanostructures with the ability to catalyze different chemical reactions, paving the way to develop minimalistic enzyme-like nanomaterials. Catalytic amyloid-like assemblies have emerged among the most versatile and active, but they often require additional factors for activity. Elucidating how these factors influence the structure and activity is key for the design. Here, we showed that biologically relevant metal ions can guide and modulate the self-assembly of a small peptide into diverse amyloid architectures. The morphology and catalytic activity of the resulting fibrils were tuned by the specific metal ion decorating the surface, whereas X-ray structural analysis of the amyloids showed ion-dependent shape sizes. Molecular dynamics simulations showed that the metals can strongly affect the local conformational space, which can trigger major rearrangements of the fibrils. Our results demonstrate that the conformational landscape of catalytic amyloids is broad and tunable by external factors, which can be critical for future design strategies.

摘要

理性设计肽已成为产生具有催化不同化学反应能力的自组装纳米结构的有力工具,为开发简约型酶纳米材料铺平了道路。催化类淀粉样组装体在多功能和高活性方面脱颖而出,但它们通常需要额外的因素才能发挥活性。阐明这些因素如何影响结构和活性对于设计至关重要。在这里,我们表明,生物相关的金属离子可以指导和调节小分子肽自组装成不同的淀粉样结构。表面装饰的特定金属离子可调节所得纤维的形态和催化活性,而对淀粉样蛋白的 X 射线结构分析表明,离子的形状尺寸具有依赖性。分子动力学模拟表明,金属可以强烈影响局部构象空间,从而引发纤维的重大重排。我们的结果表明,催化淀粉样蛋白的构象景观广泛且可通过外部因素进行调节,这对于未来的设计策略可能至关重要。

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