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Active site engineering of Zn-doped mesoporous ceria toward highly efficient organophosphorus hydrolase-mimicking nanozyme.
Lee, Junsang; Le, Xuan Ai; Chun, Hoje; Vu, Trung Hieu; Choi, Daeeun; Han, Byungchan; Kim, Moon Il; Lee, Jinwoo.
Afiliação
  • Lee J; Department of Chemical and Biomolecular Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, 34141, Republic of Korea.
  • Le XA; Department of BioNano Technology, Gachon University, Seongnam, Gyeonggi, 13120, Republic of Korea.
  • Chun H; Department of Chemical and Biomolecular Engineering, Yonsei University, Seoul, 03722, Republic of Korea.
  • Vu TH; Department of BioNano Technology, Gachon University, Seongnam, Gyeonggi, 13120, Republic of Korea.
  • Choi D; Department of Chemical and Biomolecular Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, 34141, Republic of Korea.
  • Han B; Department of Chemical and Biomolecular Engineering, Yonsei University, Seoul, 03722, Republic of Korea. Electronic address: bchan@yonsei.ac.kr.
  • Kim MI; Department of BioNano Technology, Gachon University, Seongnam, Gyeonggi, 13120, Republic of Korea. Electronic address: moonil@gachon.ac.kr.
  • Lee J; Department of Chemical and Biomolecular Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, 34141, Republic of Korea. Electronic address: jwlee1@kaist.ac.kr.
Biosens Bioelectron ; 246: 115882, 2024 Feb 15.
Article em En | MEDLINE | ID: mdl-38043302
ABSTRACT
Hydrolase-mimicking nanozymes have received increasing attention in recent years, but the effective rational design and development of these materials has not been realized, as they are not at present considered a critical research target. Herein, we report that Zn-doped mesoporous ceria (Zn-m-ceria) engineered to have an abundance of two different active sites with different functions-one that allows both co-adsorption binding of organophosphate (OP) and water and another that serves as a general base-has significant organophosphorus hydrolase (OPH)-like catalytic activity. Specifically, Zn-m-ceria exhibits a catalytic efficiency over 75- and 25-fold higher than those of m-ceria and natural OPH, respectively. First-principles calculations reveal the importance of Zn for the OPH-mimicking activity of the material, promoting substrate adsorption and proton-binding. The OPH-like Zn-m-ceria catalyst is successfully applied to detect a model OP, methyl paraoxon, in spiked tap water samples with excellent sensitivity, stability, and detection precision. We expect that these findings will promote research based on the rational engineering of the active site of nanozymes and efficient strategies for obtaining a diverse range of catalysts that mimic natural enzymes, and hence the utilization in real-world applications of enzyme-mimicking catalysts with properties superior to their natural analogs should follow.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Técnicas Biossensoriais / Arildialquilfosfatase Idioma: En Revista: Biosens Bioelectron Assunto da revista: BIOTECNOLOGIA Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Técnicas Biossensoriais / Arildialquilfosfatase Idioma: En Revista: Biosens Bioelectron Assunto da revista: BIOTECNOLOGIA Ano de publicação: 2024 Tipo de documento: Article
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