| Literature DB >> 33720739 |
Si Sun1, Haile Liu1, Qi Xin2, Ke Chen1, Huizhen Ma1, Shuhu Liu3, Xiaoyu Mu2, Wenting Hao2, Shuangjie Liu2, Yalong Gao4, Yang Wang2, Jiahui Pei1, Ruoli Zhao1, Shaofang Zhang1, Xiaoning Zhang2, Hao Wang2, Yonghui Li1, Xiao-Dong Zhang1,2.
Abstract
Natural enzymes are efficient and versatile biocatalysts but suffer in their environmental tolerance and catalytic stability. As artificial enzymes, nanozymes can improve the catalytic stability, but it is still a challenge to achieve high catalytic activity. Here, we employed atomic engineering to build the artificial enzyme named Au24Ag1 clusterzyme that hosts an ultrahigh catalytic activity as well as strong physiological stability via atom manipulation. The designed Au24Ag1 clusterzyme activates the Ag-S active site via lattice expansion in the oligomer atom layer, showing an antioxidant property 72 times higher than that of natural antioxidant Trolox. Enzyme-mimicked studies find that Au24Ag1 clusterzyme exhibits high catalase-like (CAT-like) and glutathione peroxidase-like (GPx-like) activity with a maximum reaction rate of 68.9 and 17.8 μM/min, respectively. Meanwhile, the unique catalytic landscape exhibits distinctive reactions against inflammation by inhibiting the cytokines at an early stage in the brain. Atomic engineering of clusterzymes provides a powerful and attractive platform with satisfactory atomic dispersion for tailoring biocatalysts freely at the atomic level.Entities:
Keywords: Acute Inflammation; Atomic Engineering; Clusterzyme
Mesh:
Substances:
Year: 2021 PMID: 33720739 DOI: 10.1021/acs.nanolett.0c05148
Source DB: PubMed Journal: Nano Lett ISSN: 1530-6984 Impact factor: 11.189