State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Key Laboratory for Bio-Nanotechnology and Molecular Engineering of Hunan Province, Hunan University, Changsha, 410082, China.
Chembiochem. 2018 Oct 4;19(19):2099-2106. doi: 10.1002/cbic.201800337. Epub 2018 Aug 20.
Spatial organization of multiple enzymes at specific positions for a controlled reaction cascade has attracted wide attention in recent years. Here, we report the construction of a biomimetic enzyme cascade organized on DNA triangle prism (TP) nanostructures to enable the efficient catalytic production of nitric oxide (NO) on a single microbead. Two enzymes, glucose oxidase (GOx) and horseradish peroxidase (HRP), were assembled at adjacent locations on a DNA TP nanostructure by using DNA-binding protein adaptors with small interenzyme distances. In the cascade, the first enzyme, GOx, converts glucose into gluconic acid in the presence of oxygen. The produced H O intermediate is rapidly transported to the second enzyme, HRP, which oxides hydroxyurea into NO and other nitroxyl species. The pH near the surface of the negatively charged DNA nanostructures is believed to be lower than that in the bulk solution; this creates an optimal pH environment for the anchored enzymes, which results in higher yields of the NO product. Furthermore, the multienzyme system was immobilized on a microbead mediated by a DNA adaptor, and this enabled the efficient catalytic generation of gas molecules in the microreactor. Therefore, this work provides an alternative route for the biomimetic generation of NO through enzyme cascades. In particular, the dynamic binding capability of the DNA sequence enabled the positions of the protein enzyme and the DNA nanostructure to be reversed, which allowed the cascade catalysis to be modulated.
近年来,人们对将多种酶在特定位置进行空间组织以实现可控的级联反应引起了广泛关注。在这里,我们报告了在 DNA 三角棱镜(TP)纳米结构上构建仿生酶级联系统,以实现在单个微球上高效催化生成一氧化氮(NO)。通过使用具有小酶间距离的 DNA 结合蛋白接头,将两种酶,葡萄糖氧化酶(GOx)和辣根过氧化物酶(HRP)组装在 DNA TP 纳米结构的相邻位置上。在级联反应中,第一酶 GOx 在氧气存在下将葡萄糖转化为葡萄糖酸。产生的 H2O2 中间体被迅速运送到第二个酶 HRP,后者将羟脲氧化成 NO 和其他硝酰基物质。带负电荷的 DNA 纳米结构表面附近的 pH 值被认为低于体相溶液中的 pH 值;这为固定化酶创造了一个最佳的 pH 环境,从而提高了 NO 产物的产量。此外,多酶系统通过 DNA 接头固定在微球上,这使得在微反应器中能够有效地催化生成气体分子。因此,这项工作为通过酶级联仿生生成 NO 提供了一种替代途径。特别是,DNA 序列的动态结合能力使蛋白质酶和 DNA 纳米结构的位置能够反转,从而可以调节级联催化。