Atom-pair engineering of single-atom nanozyme for boosting peroxidase-like activity.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 39134525.
- Also identified by DOI 10.1038/s41467-024-51022-4 and PMC identifier 11319669.
- Licence recorded as CC BY-NC-ND.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
Constructing atom-pair engineering and improving the activity of metal single-atom nanozyme (SAzyme) is significant but challenging. Herein, we design the atom-pair engineering of Zn-SA/CNCl SAzyme by simultaneously constructing Zn-N<sub>4</sub> sites as catalytic sites and Zn-N<sub>4</sub>Cl<sub>1</sub> sites as catalytic regulator. The Zn-N<sub>4</sub>Cl<sub>1</sub> catalytic regulators effectively boost the peroxidase-like activities of Zn-N<sub>4</sub> catalytic sites, resulting in a 346-fold, 1496-fold, and 133-fold increase in the maximal reaction velocity, the catalytic constant and the catalytic efficiency, compared to Zn-SA/CN SAzyme without the Zn-N<sub>4</sub>Cl<sub>1</sub> catalytic regulator. The Zn-SA/CNCl SAzyme with excellent peroxidase-like activity effectively inhibits tumor cell growth in vitro and in vivo. The density functional theory (DFT) calculations reveal that the Zn-N<sub>4</sub>Cl<sub>1</sub> catalytic regulators facilitate the adsorption of <sup>*</sup>H<sub>2</sub>O<sub>2</sub> and re-exposure of Zn-N<sub>4</sub> catalytic sites, and thus improve the reaction rate. This work provides a rational and effective strategy for improving the peroxidase-like activity of metal SAzyme by atom-pair engineering.
Medical subject headings
- Peroxidase
- Zinc