Chimeric Biocatalyst Combining Peptidic and Nucleic Acid Components Overcomes the Performance and Limitations of the Native Horseradish Peroxidase

  • Xiaobo Zhang
  • , Dehui Qiu
  • , Jielin Chen
  • , Yue Zhang
  • , Jiawei Wang
  • , Desheng Chen
  • , Yuan Liu
  • , Mingpan Cheng
  • , David Monchaud
  • , Jean Louis Mergny
  • , Huangxian Ju
  • , Jun Zhou

Research output: Contribution to journalArticlepeer-review

Abstract

Chimeric peptide-DNAzyme (CPDzyme) is a novel artificial peroxidase that relies on the covalent assembly of DNA, peptides, and an enzyme cofactor in a single scaffold. An accurate control of the assembly of these different partners allows for the design of the CPDzyme prototype G4-Hemin-KHRRH, found to be >2000-fold more active (in terms of conversion number kcat) than the corresponding but non-covalent G4/Hemin complex and, more importantly, >1.5-fold more active than the corresponding native peroxidase (horseradish peroxidase) when considering a single catalytic center. This unique performance originates in a series of gradual improvements, thanks to an accurate selection and arrangement of the different components of the CPDzyme, in order to benefit from synergistic interactions between them. The optimized prototype G4-Hemin-KHRRH is efficient and robust as it can be used under a wide range of non-physiologically relevant conditions [organic solvents, high temperature (95 °C), and in a wide range of pH (from 2 to 10)], thus compensating for the shortcomings of the natural enzymes. Our approach thus opens broad prospects for the design of ever more efficient artificial enzymes.

Original languageEnglish
Pages (from-to)4517-4526
Number of pages10
JournalJournal of the American Chemical Society
Volume145
Issue number8
DOIs
Publication statusPublished - 1 Mar 2023

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