Synergetic Enzyme-Incorporated Metal-Organic Framework and Polyoxometalate Nanozyme: Achieving Stable Tandem Catalysis for Organic Photoelectrochemical Transistor Bioanalysis

被引:3
|
作者
Zhang, Xiao-Cui [1 ,2 ,3 ,4 ]
Hou, Lu [3 ,4 ]
Cai, Huihui [3 ]
Zhang, Jin-Ming [3 ]
Chen, Feng-Zao [3 ]
Peng, Jinyun [1 ,2 ]
Zhao, Wei-Wei [4 ]
机构
[1] Guangxi Normal Univ Nationalities, Coll Chem & Chem Engn, Chongzuo 532200, Peoples R China
[2] Henan Univ Chinese Med, Sch Pharm, Zhengzhou 450046, Peoples R China
[3] Taizhou Univ, Sch Pharmaceut & Chem Engn, Taizhou 318000, Peoples R China
[4] Nanjing Univ, Sch Chem & Chem Engn, State Key Lab Analyt Chem Life Sci, Nanjing 210023, Peoples R China
基金
中国国家自然科学基金;
关键词
D O I
10.1021/acs.analchem.4c03786
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Organic photoelectrochemical transistor (OPECT) has emerged as a promising technique for biomolecule detection, yet its operational rationale remains limited due to its short development time. This study introduces a stable tandem catalysis protocol by synergizing the enzyme-incorporated metal-organic frameworks (E-MOFs) with polyoxometalate (POM) nanozyme for sensitive OPECT bioanalysis. The zeolitic imidazolate framework-8 (ZIF-8) acts as the skeleton to protect the encapsulated glucose oxidase (GOx), allowing the stable catalytic generation of H2O2. With peroxidase-like activity, a phosphotungstic acid hydrate (PW12) is then able to utilize the H2O2 to induce the biomimetic precipitation on the photogate, ultimately resulting in the altered device characteristics for quantitative detection. This work reveals the potential and versatility of an engineered enzymatic system as a key enabler to achieve novel OPECT bioanalysis, which is believed to offer a feasible framework to explore new operational rationale in optoelectronic and bioelectronic detection.
引用
收藏
页码:16355 / 16361
页数:7
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