催化作用
配位复合体
金属
化学
辣根过氧化物酶
水溶液中的金属离子
基质(水族馆)
无机化学
组合化学
酶
有机化学
海洋学
地质学
作者
Jiaxin Dong,Guanxiong Liu,Yu. V. Petrov,Yujie Feng,Dechang Jia,В. Е. Баулин,A. Yu. Tsivadze,Yu Zhang,Baoqiang Li
出处
期刊:ACS materials letters
[American Chemical Society]
日期:2024-02-26
卷期号:6 (4): 1112-1119
标识
DOI:10.1021/acsmaterialslett.4c00109
摘要
Metal ion-carbon based nanomaterials served as nanozymes to mimic the biocatalytic performance of natural enzymes. However, there are still challenges in constructing carbon dots (CDs)–metal nanozymes with the same coordination structure based on coordination chemistry and revealing the effect of metal ion species on enzyme-mimicking catalyzed activities. Herein, EDTA-functionalized carbon dots–metal (CDsEDTA-Me) nanozymes with different metal ions (Fe3+, Cu2+, and Co2+) and the same coordination structures are synthesized based on coordination chemistry. Species of metal ions of CDsEDTA-Me nanozymes determines enzyme-mimicking activities. CDsEDTA-Fe, CDsEDTA-Cu, and CDsEDTA-Co display significant peroxidase (POD)-mimicking, superoxide dismutase (SOD)-mimicking activities, and hydroxyl radical (•OH) scavenging ability, respectively. Compared with horseradish peroxidase, the affinity of CDsEDTA-Fe to H2O2 is improved by 47 times. The Vm value of CDsEDTA-Fe with TMB as the substrate is 1.19 × 10–7 M s–1. POD-mimicking activity of CDsEDTA-Me nanozymes increases linearly with the increase of stability constants of CDsEDTA-Me, which indicates that the POD-mimicking activity of CDsEDTA-Me can be predicted by stability constants of CDsEDTA-Me. CDsEDTA-Me provides a coordination chemistry strategy for the construction of CDs-metal nanozymes and rational improvement of enzyme-mimicking activities.
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