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Construction of GPx active centers on natural protein nanodiskanotube: A new way to develop artificial nanoenzyme

机译:在天然蛋白质纳米盘/纳米管上构建GPx活性中心:开发人工纳米酶的新方法

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摘要

Construction of catalytic centers on natural protein aggregates is a challenging topic in biomaterial and biomedicine research. Here we report a novel construction of artificial nanoenzyme with glutathione peroxidase (GPx)-like function. By engineering the surface of tobacco mosaic virus (TMV) coat protein, the main catalytic components of GPx were fabricated on TMV protein monomers. Through direct self-assembly of the functionalized viral coat proteins, the multi-GPx centers were installed on these well-defined nanodisks or nanotubes. With the help of muti-selenoenzyme centers, the resulting organized nanoenzyme exhibited remarkable GPx activity, even approaching the level of natural GPx. The antioxidation study on subcell mitochondrial level demonstrated that virus-based nanoenzyme exerted excellent capacity for protecting cell from oxidative damage. This strategy represents a new way to develop artificial nanoenzymes.
机译:在天然材料聚集体上建立催化中心是生物材料和生物医学研究中的一个具有挑战性的主题。在这里,我们报告具有谷胱甘肽过氧化物酶(GPx)样功能的人工纳米酶的新型结构。通过修饰烟草花叶病毒(TMV)外壳蛋白的表面,在TMV蛋白单体上制备了GPx的主要催化成分。通过功能化病毒外壳蛋白的直接自组装,将多个GPx中心安装在这些定义明确的纳米盘或纳米管上。在多硒酶中心的帮助下,所得的有组织的纳米酶表现出显着的GPx活性,甚至接近天然GPx的水平。对亚细胞线粒体水平的抗氧化研究表明,基于病毒的纳米酶具有出色的保护细胞免受氧化损伤的能力。该策略代表了开发人工纳米酶的新方法。

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