A Library of ROS-Catalytic Metalloenzyme Mimics with Atomic Metal Centers

Adv Mater. 2022 Apr;34(16):e2200255. doi: 10.1002/adma.202200255. Epub 2022 Mar 1.

Abstract

MetalN-coordinated centers supported by carbonaceous substrates have emerged as promising artificial metalloenzymes (AMEs) to mimic the biocatalytic effects of their natural counterparts. However, the synthesis of well-defined AMEs that contain different atomic metalN centers but present similar physicochemical and coordination structures remains a substantial challenge. Here, 20 different types of AMEs with similar geometries and well-defined atomic metalN-coordinated centers are synthesized to compare and disclose the catalytic activities, substrate selectivities, kinetics, and reactive oxygen species (ROS) products. Their oxidase (OXD)-, peroxidase (POD)-, and halogen peroxidase (HPO)-mimetic catalytic behaviors are systematically explored. The Fe-AME shows the highest OXD- and HPO-mimetic activities compared to the other AMEs due to its high vmax (0.927 × 10-6 m s-1 ) and low Km (1.070 × 10-3 m), while the Cu-AME displays the best POD-like performance. Furthermore, theoretical calculation reveals that the ROS-catalytic paths and activities are highly related to the electronic structures of the metal centers. Benefiting from its facile adsorption of H2 O2 molecule and lower energy barrier to generating •O2 - , the Fe-AME displays higher ROS-catalytic performances than the Mn-AME. The engineered AMEs show not only remarkably high ROS-catalytic performances but also provide new guidance toward developing metalN-coordinated biocatalysts for broad application fields.

Keywords: biocatalysts; biomaterials; catalytic ROS generation; enzyme mimics; metal N-coordinated centers.

MeSH terms

  • Catalysis
  • Metalloproteins*
  • Metals
  • Oxidoreductases
  • Peroxidase* / chemistry
  • Peroxidases
  • Reactive Oxygen Species

Substances

  • Metalloproteins
  • Metals
  • Reactive Oxygen Species
  • Oxidoreductases
  • Peroxidases
  • Peroxidase