高负载Cu单原子纳米酶的制备和类酶活性研究
作者:
作者单位:

1)天津大学医学工程与转化医学研究院,天津 300072;2)天津大学理学院,天津 300350

作者简介:

张晓东 Tel:022-83612122,E-mail:xiaodongzhang@tju.edu.cnZHANG Xiao-Dong. Tel: 86-22-83612122, E-mail: xiaodongzhang@tju.edu.cn

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基金项目:

国家重点研发计划(2021YFF1200700),国家自然科学基金(91859101,81971744,U1932107,82001952,11804248),天津市杰出青年基金(2021FJ-0009),天津市自然科学基金(19JCZDJC34000,20JCYBJC00940,21JCYBJC00550,21JCZDJC00620, 21JCYBJC00490),天津大学创新基金和中国科学院创新交叉团队(JCTD-2020-08)资助项目。


Design and Enzyme-mimicking Activity of High-loading Cu Single-atom Nanozyme
Author:
Affiliation:

1)Academy of Medical Engineering and Translational Medicine, Tianjin University, Tianjin 300072, China;2)School of Sciences, Tianjin University, Tianjin 300350, China

Fund Project:

This work was supported by grants from the National Key Research and Development Program of China (2021YFF1200700), The National Natural Science Foundation of China (91859101, 81971744, U1932107, 82001952, 11804248), Outstanding Youth Funds of Tianjin (2021FJ-0009), National Natural Science Foundation of Tianjin (19JCZDJC34000, 20JCYBJC00940, 21JCYBJC00550, 21JCZDJC00620, 21JCYBJC00490), the Innovation Foundation of Tianjin University, and CAS Interdisciplinary Innovation Team (JCTD-2020-08).

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    摘要:

    目的 单原子纳米酶(single-atom nanozyme,SAN)因其高原子利用率及丰富的类酶活性被广泛研究。但是目前大多数SAN活性位点负载量较低,限制了其进一步应用和发展。本研究旨在制备一种高原子负载量的SAN,并对其类酶活性进行系统研究,希望为高负载SAN的制备提供思路,并为SAN在更广泛领域的应用提供理论支持。方法 本研究通过原位锚定策略将金属盐前驱体锚定在氨基化石墨烯量子点框架中,在惰性气体保护下进行高温热解稳定Cu原子和载体之间的化学键,制备出负载量高达7.66%(质量百分比)的高负载Cu单原子纳米酶(high-loading Cu SAN)。此外,以3,3",5,5"-四甲基联苯胺(TMB)和氮蓝四唑(NBT)为显色剂,评估了high-loading Cu SAN的类过氧化物酶(POD)、类氧化物酶(OXD)及类超氧化物歧化酶(SOD)活性,并与传统金属有机框架锚定法制备的低负载Cu单原子纳米酶(low-loading Cu SAN)作比较。以过氧化氢(H2O2)为催化底物,对比研究了高/低负载Cu SAN的类过氧化氢酶(CAT)活性。结果 研究表明,本文制备的高负载Cu SAN的类POD和SOD活性分别是低负载Cu SAN的3.4倍和8.88倍,且表现出类酶催化选择性。结论 本研究为高负载SAN的制备和活性研究提供了思路,为SAN在检测传感、疾病治疗以及环境保护等方面的应用奠定了基础。

    Abstract:

    Objective Recently, single-atom nanozyme (SAN) has been widely studied due to its high atom utilization and various enzyme-mimicking activities. However, most of the SANs present low metal-atom densities, which restrict their further application and development. The aim of this study is to prepare SAN with high atomic loading and to systematically investigate its enzyme-like activities, in the hope of providing ideas for the preparation of highly loaded SANs and theoretical support for the application of SANs in a wider range of fields.Methods In this work, high-loading Cu SAN with metal contents up to 7.66% (w/w) was prepared using in-situ anchoring strategy. The metal salt precursors were confined into the carbon carriers consisting of aminated graphene quantum dots, and then urea was introduced to provide a rich N-coordination environment for Cu atoms. The chemical bond between Cu atoms and the carrier was further stabilized by pyrolysis under the protection of Ar gas. The low-loading Cu SAN used for comparison was prepared according to traditional metal organic framework (MOFs) anchoring method. Then, the peroxidase (POD)-like, oxidase (OXD)-like and superoxide dismutase (SOD)-like catalytic activities of high/low-loading Cu SAN were tested and compared with 3,3",5,5"- tetramethylbenzidine (TMB) and nitrotetrazolium blue chloride (NBT) as chromogenic substrates. The catalase (CAT)-like catalytic activities of high/low-loading Cu SAN were assessed by monitoring the decomposition rate of hydrogen peroxide (H2O2).Results The results suggested that the high-loading Cu SAN possesses the improved catalytic activity and selectivity towards POD-like and SOD-like activities, showing 3.4-fold and 8.88-fold higher than low-loading Cu SAN, respectively.Conclusion This work provides a strategy to synthesize SAN with high metal-atom density. And the results show that atomic regulation can be achieved by adjusting preparation methods which assist to obtain SAN with different catalytic selectivity, and lay foundation for the development and application of SAN in detection and sensing, diseases treatment and environmental protection.

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陈心珠,刘晓宇,张少芳,穆晓宇,张晓东.高负载Cu单原子纳米酶的制备和类酶活性研究[J].生物化学与生物物理进展,2023,50(11):2684-2696

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  • 收稿日期:2022-11-14
  • 最后修改日期:2023-08-25
  • 接受日期:2023-01-28
  • 在线发布日期: 2023-11-22
  • 出版日期: 2023-11-20