Deciphering the catalytic mechanism of superoxide dismutase activity of carbon dot nanozyme.
Wenhui GaoJiuyang HeLei ChenXiangqin MengYana MaLiangliang ChengKangsheng TuXuejiao J GaoCui LiuMingzhen ZhangKelong FanDai-Wen PangXiyun YanPublished in: Nature communications (2023)
Nanozymes with superoxide dismutase (SOD)-like activity have attracted increasing interest due to their ability to scavenge superoxide anion, the origin of most reactive oxygen species in vivo. However, SOD nanozymes reported thus far have yet to approach the activity of natural enzymes. Here, we report a carbon dot (C-dot) SOD nanozyme with a catalytic activity of over 10,000 U/mg, comparable to that of natural enzymes. Through selected chemical modifications and theoretical calculations, we show that the SOD-like activity of C-dots relies on the hydroxyl and carboxyl groups for binding superoxide anions and the carbonyl groups conjugated with the π-system for electron transfer. Moreover, C-dot SOD nanozymes exhibit intrinsic targeting ability to oxidation-damaged cells and effectively protect neuron cells in the ischemic stroke male mice model. Together, our study sheds light on the structure-activity relationship of C-dot SOD nanozymes, and demonstrates their potential for treating of oxidation stress related diseases.
Keyphrases
- amyotrophic lateral sclerosis
- hydrogen peroxide
- induced apoptosis
- electron transfer
- cell cycle arrest
- energy transfer
- ionic liquid
- structure activity relationship
- photodynamic therapy
- nitric oxide
- molecular dynamics
- risk assessment
- signaling pathway
- mass spectrometry
- density functional theory
- cell proliferation
- transcription factor
- dna binding