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通过铜配体配位,合理设计具有稳健催化性能的聚合物纳米酶。

Rational design of polymeric nanozymes with robust catalytic performance via copper-ligand coordination.

机构信息

State-Key Laboratory of Chemical Engineering, and Shanghai Key Laboratory of Multiphase Materials Chemical Engineering, East China University of Science and Technology, 130, Meilong Road, 200237 Shanghai, People's Republic of China.

State-Key Laboratory of Chemical Engineering, and Shanghai Key Laboratory of Multiphase Materials Chemical Engineering, East China University of Science and Technology, 130, Meilong Road, 200237 Shanghai, People's Republic of China.

出版信息

J Colloid Interface Sci. 2023 Sep;645:458-465. doi: 10.1016/j.jcis.2023.04.142. Epub 2023 May 3.

Abstract

Incorporating copper (Cu) ions into polymeric particles can be a straightforward strategy for mimicking copper enzymes, but it is challenging to simultaneously control the structure of the nanozyme and of the active sites. In this report, we present a novel bis-ligand (L) containing bipyridine groups connected by a tetra-ethylene oxide (4EO) spacer. In phosphate buffer the Cu-L mixture forms coordination complexes that (at proper composition) can bind polyacrylic acid (PAA) to produce catalytically active polymeric nanoparticles with well-defined structure and size, which we refer to as 'nanozymes'. Manipulating the L/Cu mixing ratio and using phosphate as a co-binding motif, cooperative copper centres are realized that exhibit promoted oxidation activity. The structure and activity of the so-designed nanozymes remain stable upon increasing temperature and over multiple cycles of application. Increasing ionic strength causes enhanced activity, a response also seen for natural tyrosinase. By means of our rational design we obtain nanozymes with optimized structure and active sites that in several respects outperform natural enzymes. This approach therefore demonstrates a novel strategy for developing functional nanozymes, which may well stimulate the application of this class of catalysts.

摘要

将铜(Cu)离子掺入聚合物颗粒中是模拟铜酶的一种简单策略,但同时控制纳米酶和活性位点的结构具有挑战性。在本报告中,我们提出了一种新型的双配体(L),其中包含通过四乙撑氧化物(4EO)间隔臂连接的双吡啶基团。在磷酸盐缓冲液中,Cu-L 混合物形成配位复合物,(在适当的组成下)可以将聚丙烯酸(PAA)结合,从而产生具有明确定义结构和尺寸的催化活性聚合物纳米颗粒,我们称之为“纳米酶”。通过操纵 L/Cu 混合比并使用磷酸盐作为共结合基序,可以实现协同铜中心,表现出促进的氧化活性。所设计的纳米酶的结构和活性在升高温度和多次应用循环中保持稳定。增加离子强度会导致活性增强,天然酪氨酸酶也表现出这种反应。通过我们的合理设计,我们获得了具有优化结构和活性位点的纳米酶,在几个方面优于天然酶。因此,这种方法为开发功能性纳米酶提供了一种新策略,可能会刺激这类催化剂的应用。

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