Wu Weiwei, Huang Liang, Zhu Xinyang, Chen Jinxing, Chao Daiyong, Li Minghua, Wu Shuangli, Dong Shaojun
State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences Changchun Jilin 130022 China.
University of Science and Technology of China Hefei Anhui 230026 China.
Chem Sci. 2022 Mar 24;13(16):4566-4572. doi: 10.1039/d2sc00212d. eCollection 2022 Apr 20.
Mechanism research of nanozymes has always been of great interest since their emergence as outstanding mimics of friable natural enzymes. An important but rarely mentioned issue in mechanism research of nanozymology is the inhibitory effect of nanozymes. And conventional nanozymes with various active sites hinder the mechanism research, while single-atom Fe-N-C nanozymes with similar active sites to natural enzymes exhibit structural advantages. Herein, we synthesized Fe single-atom nanozymes (Fe-SANs) with ultrahigh oxidase-like activity and found that a common analgesic-antipyretic drug 4-acetamidophenol (AMP) had inhibitory effects for the oxidase-like activity of Fe-SANs. We investigated the inhibitory effects in detail and demonstrated that the inhibition type was reversible mixed-inhibition with inhibition constants ( and ) of 0.431 mM and 0.279 mM, respectively. Furthermore, we put forward a colorimetric method for AMP detection based on nanozyme inhibition. The research on the inhibitory effects of small molecules on nanozymes expands the scope of analysis based on nanozymes and the inhibition mechanism study may offer some insight into investigating the interaction between nanozymes and inhibitors.
自纳米酶作为天然易碎酶的杰出模拟物出现以来,其作用机制的研究一直备受关注。纳米酶学机制研究中一个重要但很少被提及的问题是纳米酶的抑制作用。具有各种活性位点的传统纳米酶阻碍了机制研究,而与天然酶具有相似活性位点的单原子Fe-N-C纳米酶则具有结构优势。在此,我们合成了具有超高类氧化酶活性的铁单原子纳米酶(Fe-SANs),并发现一种常见的解热镇痛药对乙酰氨基酚(AMP)对Fe-SANs的类氧化酶活性具有抑制作用。我们详细研究了其抑制作用,证明抑制类型为可逆混合抑制,抑制常数( 和 )分别为0.431 mM和0.279 mM。此外,我们提出了一种基于纳米酶抑制的AMP比色检测方法。小分子对纳米酶抑制作用的研究扩展了基于纳米酶的分析范围,抑制机制研究可能为研究纳米酶与抑制剂之间的相互作用提供一些见解。