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Ultrahigh peroxidase-like catalytic performance of Cu -N 4 and Cu -N 4 S active sites-containing reduced graphene oxide for sensitive electrochemical biosensing

Authors
Le, Phan GiaLe, Xuan AiDuong, Hai SangJung, Sung HoonKim, TaeYoungKim, Moon Il
Issue Date
Jul-2024
Publisher
ELSEVIER ADVANCED TECHNOLOGY
Keywords
Acetylcholine detection; Electrochemical biosensing; Graphene oxide; Heteroatom doping; Single-atom nanozyme
Citation
Biosensors and Bioelectronics, v.255
Journal Title
Biosensors and Bioelectronics
Volume
255
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/91511
DOI
10.1016/j.bios.2024.116259
ISSN
0956-5663
1873-4235
Abstract
Carbon-based nanozymes possessing peroxidase-like activity have attracted significant interest because of their potential to replace native peroxidases in biotechnology. Although various carbon-based nanozymes have been developed, their relatively low catalytic efficiency needs to be overcome to realize their practical utilization. Here, inspired by the elemental uniqueness of Cu and the doped elements N and S, as well as the active site structure of Cu-centered oxidoreductases, we developed a new carbon-based peroxidase-mimicking nanozyme, single-atom Cu-centered N- and S-codoped reduced graphene oxide (Cu-NS-rGO), which preserved many Cu–N4 and Cu–N4S active sites and showed dramatically high peroxidase-like activity without any oxidase-like activity, yielding up to 2500-fold higher catalytic efficiency (kcat/Km) than that of pristine rGO. The high catalytic activity of Cu-NS-rGO might be attributed to the acceleration of electron transfer from Cu single atom as well as synergistic effects from both Cu–N4 and Cu–N4S active sites, which was theoretically confirmed by Gibbs free energy calculations using density functional theory. The prepared Cu-NS-rGO was then used to construct an electrochemical bioassay system for detecting choline and acetylcholine by coupling with the corresponding oxidases. Using this system, both target molecules were selectively determined with high sensitivity that was sufficient to clinically determine their levels in physiological fluids. Overall, this study will facilitate the development of nanocarbon-based nanozymes and their electrochemical biosensing applications, which can be extended to the development of miniaturized devices in point-of-care testing environments. © 2024 Elsevier B.V.
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반도체대학 (반도체·전자공학부)
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