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由 MOF 衍生的多孔碳负载原子分散的 Fe-N 配位结构的单原子纳米酶表现出前所未有的过氧化物酶模拟活性。

Unprecedented peroxidase-mimicking activity of single-atom nanozyme with atomically dispersed Fe-N moieties hosted by MOF derived porous carbon.

机构信息

School of Mechanical and Materials Engineering, Washington State University, Pullman, WA, 99164, USA.

Health Impacts & Exposure Science, Pacific Northwest National Laboratory, Richland, WA, 99352, USA.

出版信息

Biosens Bioelectron. 2019 Oct 1;142:111495. doi: 10.1016/j.bios.2019.111495. Epub 2019 Jul 10.

DOI:10.1016/j.bios.2019.111495
PMID:31310943
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8672370/
Abstract

Due to robustness, easy large-scale preparation and low cost, nanomaterials with enzyme-like characteristics (defined as 'nanozymes') are attracting increasing interest for various applications. However, most of currently developed nanozymes show much lower activity in comparison with natural enzymes, and the deficiency greatly hinders their use in sensing and biomedicine. Single-atom catalysts (SACs) offer the unique feature of maximum atomic utilization, providing a potential pathway to improve the catalytic activity of nanozymes. Herein, we propose a Fe-N-C single-atom nanozyme (SAN) that exhibits unprecedented peroxidase-mimicking activity. The SAN consists of atomically dispersed Fe─N moieties hosted by metal-organic frameworks (MOF) derived porous carbon. Thanks to the 100% single-atom active Fe dispersion and the large surface area of the porous support, the Fe-N-C SAN provided a specific activity of 57.76 U mg, which was almost at the same level as natural horseradish peroxidase (HRP). Attractively, the SAN presented much better storage stability and robustness against harsh environments. As a proof-of-concept application, highly sensitive biosensing of butyrylcholinesterase (BChE) activity using the Fe-N-C SAN as a substitute for natural HRP was further verified.

摘要

由于具有稳健性、易于大规模制备和低成本等特点,具有类酶特性的纳米材料(定义为“纳米酶”)因其在各种应用中的应用而引起了越来越多的关注。然而,与天然酶相比,目前开发的大多数纳米酶的活性要低得多,这一缺陷极大地阻碍了它们在传感和生物医学中的应用。单原子催化剂 (SAC) 具有最大原子利用率的独特特性,为提高纳米酶的催化活性提供了一条潜在途径。在此,我们提出了一种具有空前过氧化物酶模拟活性的 Fe-N-C 单原子纳米酶 (SAN)。SAN 由金属有机框架 (MOF) 衍生的多孔碳负载的原子分散的 Fe─N 基团组成。由于 100%的单原子活性 Fe 分散和多孔载体的大表面积,Fe-N-C SAN 的比活性达到 57.76 U mg,几乎与天然辣根过氧化物酶 (HRP) 相当。引人注目的是,SAN 表现出更好的储存稳定性和对恶劣环境的鲁棒性。作为概念验证应用,进一步验证了使用 Fe-N-C SAN 作为天然 HRP 的替代品对丁酰胆碱酯酶 (BChE) 活性进行高灵敏度的生物传感。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c1f/8672370/2c6e4a202b40/nihms-1760759-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c1f/8672370/17813e9f6606/nihms-1760759-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c1f/8672370/cb1b27cb944c/nihms-1760759-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c1f/8672370/1e2ab509c2e7/nihms-1760759-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c1f/8672370/6ba46a3d9cc9/nihms-1760759-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c1f/8672370/2c6e4a202b40/nihms-1760759-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c1f/8672370/17813e9f6606/nihms-1760759-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c1f/8672370/cb1b27cb944c/nihms-1760759-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c1f/8672370/1e2ab509c2e7/nihms-1760759-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c1f/8672370/6ba46a3d9cc9/nihms-1760759-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c1f/8672370/2c6e4a202b40/nihms-1760759-f0005.jpg

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