4.8 Article

Single amino acid bionanozyme for environmental remediation

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NATURE COMMUNICATIONS
卷 13, 期 1, 页码 -

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NATURE PORTFOLIO
DOI: 10.1038/s41467-022-28942-0

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  1. Airforce research laboratories (AFRL)
  2. Air Force Office of Scientific Research [FA8655-21-1-7004]
  3. Science and Engineering Research Board (SERB) of India [SRG/2021/002423]
  4. IIT (BHU)
  5. National Science Foundation [CHE-1808242]
  6. Extreme Science and Engineering Discovery Environment (XSEDE) Comet computing cluster at the University of California, San Diego [TG-ENG160024]

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The study presents a simple and efficient single amino acid bionanozyme that can catalyze the rapid oxidation of phenolic contaminants and detect neurotransmitters. Compared to natural enzymes, this copper-coordinated bionanozyme is more cost-effective, efficient, and versatile.
Enzymes are extremely complex catalytic structures with immense biological and technological importance. Nevertheless, their widespread environmental implementation faces several challenges, including high production costs, low operational stability, and intricate recovery and reusability. Therefore, the de novo design of minimalistic biomolecular nanomaterials that can efficiently mimic the biocatalytic function (bionanozymes) and overcome the limitations of natural enzymes is a critical goal in biomolecular engineering. Here, we report an exceptionally simple yet highly active and robust single amino acid bionanozyme that can catalyze the rapid oxidation of environmentally toxic phenolic contaminates and serves as an ultrasensitive tool to detect biologically important neurotransmitters similar to the laccase enzyme. While inspired by the laccase catalytic site, the substantially simpler copper-coordinated bionanozyme is similar to 5400 times more cost-effective, four orders more efficient, and 36 times more sensitive compared to the natural protein. Furthermore, the designed mimic is stable under extreme conditions (pH, ionic strength, temperature, storage time), markedly reusable for several cycles, and displays broad substrate specificity. These findings hold great promise in developing efficient bionanozymes for analytical chemistry, environmental protection, and biotechnology.

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