journal article·2021-09-22

Protein-Assisted Osmium Nanoclusters with Intrinsic Peroxidase-like Activity and Extrinsic Antifouling Behavior

Shao-Bin He, Meng-Ting Lin, Liu Yang, Hamada A. A. Noreldeen, Hua-Ping Peng, Hao-Hua Deng, Wei Chen

ACS Applied Materials & Interfaces· Volume 13· Issue 37
Publisher page

Abstract

Extensive studies have laid the groundwork for understanding peroxidase-like nanozymes. However, improvements are still required before their practical applications. On one hand, it is significant to explore highly reactive nanozymes. On the other hand, it is necessary to avoid fouling formed on the surface of nanozymes, which will affect their activity and the results of H2O2 sensors or H2O2-related applications. Herein, a strategy is reported to design osmium nanoclusters (Os NCs) with the existence of bovine serum albumin (BSA) through biomineralization. BSA–Os NCs were found to possess intrinsic peroxidase-like activity with a high specific activity (6120 U/g). Studies also found that the catalytic activity of BSA–Os NCs was better than those of reported protein-assisted metal nanozymes (e.g., BSA–Pt NPs and BSA–Au NCs). More significantly, BSA has been confirmed as a protective shell to give Os NCs extrinsic antifouling property in some typical ions (e.g., Hg2+, Ag+, Pb2+, I–, Cr6+, Cu2+, Ce3+, S2–, etc.), saline (0–2 M), or protein (0–100 mg/mL) conditions. Under optimal conditions, a colorimetric sensor was established to realize a linear range of H2O2 from 1.25 to 200 μM with a low detection limit of 300 nM. On this basis, remarkable features enable a BSA–Os NCs-based colorimetric sensor to detect H2O2 from complex systems with clear color gradients. Together, this work highlights the advantages of protein-assisted Os nanozymes and provides a paragon for peroxidase-like nanozymes in H2O2-related applications.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Advanced Nanomaterials in Catalysis · Nanocluster Synthesis and Applications · Advanced biosensing and bioanalysis techniques

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Fujian Key Laboratory of Drug Target Discovery and Structural and Functional Research, School of Pharmacy, Fujian Medical University, Fuzhou 350004, China

Department of Pharmacy, The Second Affiliated Hospital of Fujian Medical University, Quanzhou 362000, China

Funding

Joint Funds for the Innovation of Science and Technology, Fujian Province · Program for Innovative Research Team in Science and Technology in Fujian Province University · Program for Innovative Leading Talents in Fujian Province · Startup Fund for scientific research, Fujian Medical University

References (49)

Show source-provided references
1. 10.1038/nnano.2007.26010.1038/nnano.2007.260 ↗
2. 10.1039/c3cs35486e10.1039/c3cs35486e ↗
3. 10.1039/C8CS00457A10.1039/C8CS00457A ↗
4. 10.1016/0141-0229(95)00174-310.1016/0141-0229(95)00174-3 ↗
5. 10.1016/j.enzmictec.2007.01.01810.1016/j.enzmictec.2007.01.018 ↗
6. 10.1002/smll.20190013310.1002/smll.201900133 ↗
7. 10.1038/s41596-018-0001-110.1038/s41596-018-0001-1 ↗
8. 10.1016/j.colsurfa.2010.08.00710.1016/j.colsurfa.2010.08.007 ↗
9. 10.1016/j.bios.2014.07.00510.1016/j.bios.2014.07.005 ↗
10. 10.1021/ac503544w10.1021/ac503544w ↗
11. 10.1016/j.jhazmat.2020.12339710.1016/j.jhazmat.2020.123397 ↗
12. 10.1039/C7CS00152E10.1039/C7CS00152E ↗
13. 10.1016/j.biomaterials.2010.11.00410.1016/j.biomaterials.2010.11.004 ↗
14. 10.1021/ac404104j10.1021/ac404104j ↗
15. 10.1016/j.snb.2016.11.14510.1016/j.snb.2016.11.145 ↗
16. 10.1016/j.aca.2017.03.02810.1016/j.aca.2017.03.028 ↗
17. 10.1016/j.aca.2013.03.03410.1016/j.aca.2013.03.034 ↗
18. 10.1007/s12274-018-2154-110.1007/s12274-018-2154-1 ↗
19. 10.1039/C5NR08358C10.1039/C5NR08358C ↗
20. 10.1103/PhysRevLett.88.13570110.1103/PhysRevLett.88.135701 ↗
21. 10.1039/C4CP03068K10.1039/C4CP03068K ↗
22. 10.1039/c4tc00049h10.1039/c4tc00049h ↗
23. 10.1021/acs.analchem.9b0522210.1021/acs.analchem.9b05222 ↗
24. 10.1039/D0TA09247A10.1039/D0TA09247A ↗
25. 10.1021/ja806804u10.1021/ja806804u ↗
26. 10.1002/wnan.160210.1002/wnan.1602 ↗
27. 10.1021/ac503636j10.1021/ac503636j ↗
28. 10.1039/C3NR06896J10.1039/C3NR06896J ↗
29. 10.1021/acsami.9b1159910.1021/acsami.9b11599 ↗
30. 10.1021/acsami.0c0522910.1021/acsami.0c05229 ↗
31. 10.1002/anie.20110029910.1002/anie.201100299 ↗
32. 10.1016/j.bios.2014.11.03210.1016/j.bios.2014.11.032 ↗
33. 10.1002/cctc.20140001110.1002/cctc.201400011 ↗
34. 10.1021/acscatal.0c0164710.1021/acscatal.0c01647 ↗
35. 10.1039/C9CC00199A10.1039/C9CC00199A ↗
36. 10.1039/C7NR03399K10.1039/C7NR03399K ↗
37. 10.1016/j.bios.2017.05.03710.1016/j.bios.2017.05.037 ↗
38. 10.1016/S0891-5849(99)00137-910.1016/S0891-5849(99)00137-9 ↗
39. 10.1016/j.snb.2016.04.03910.1016/j.snb.2016.04.039 ↗
40. 10.1039/c1cc14294a10.1039/c1cc14294a ↗
41. 10.1002/slct.20170241310.1002/slct.201702413 ↗
42. 10.1007/s00216-019-02270-710.1007/s00216-019-02270-7 ↗
43. 10.1016/j.bios.2016.10.07510.1016/j.bios.2016.10.075 ↗
44. 10.1007/s00604-020-04234-610.1007/s00604-020-04234-6 ↗
45. 10.1021/acs.jced.9b0081910.1021/acs.jced.9b00819 ↗
46. 10.1016/j.bios.2017.01.03610.1016/j.bios.2017.01.036 ↗
47. 10.1021/acs.analchem.8b0555210.1021/acs.analchem.8b05552 ↗
48. 10.1021/acs.langmuir.7b0343010.1021/acs.langmuir.7b03430 ↗
49. Goth L. · Acta Biol. Hung. · 1987 · 38 · 287