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Three-Dimensional Printable Enzymatically Active Plastics AITranslate

University of Bristol; University of Bristol; University of Bristol; University of Bristol; Aarhus University; University of Bristol;Defence Science and Technology Laboratory; Australian National University; Aarhus University; University of Bristol
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Publisher: ACS
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Abstract AITranslate

Here, we describe a facile route to the synthesis of enzymatically active highly fabricable plastics, where the enzyme is an intrinsic component of the material. This is facilitated by the formation of an electrostatically stabilized enzyme–polymer surfactant nanoconstruct, which, after lyophilization and melting, affords stable macromolecular dispersions in a wide range of organic solvents. A selection of plastics can then be co-dissolved in the dispersions, which provides a route to bespoke 3D enzyme plastic nanocomposite structures using a wide range of fabrication techniques, including melt electrowriting, casting, and piston-driven 3D printing. The resulting constructs comprising active phosphotriesterase (arPTE) readily detoxify organophosphates with persistent activity over repeated cycles and for long time periods. Moreover, we show that the protein guest molecules, such as arPTE or sfGFP, increase the compressive Young’s modulus of the plastics and that the identity of the biomolecule influences the nanomorphology and mechanical properties of the resulting materials. Overall, we demonstrate that these biologically active nanocomposite plastics are compatible with state-of-the-art 3D fabrication techniques and that the methodology could be readily applied to produce robust and on-demand smart nanomaterial structures.

KeyWords AITranslate

nanocomposite nanomorphology functional bionanomaterials enzyme nanoconjugate 3D printing melt electrowriting
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Basic Information:

DOI:https://doi.org/10.1021/acsapm.1c00845

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Citation Information:

Here, we describe a facile route to the synthesis of enzymatically active highly fabricable plastics, where the enzyme is an intrinsic component of the material. This is facilitated by the formation of an electrostatically stabilized enzyme–polymer surfactant nanoconstruct, which, after lyophilization and melting, affords stable macromolecular dispersions in a wide range of organic solvents. A selection of plastics can then be co-dissolved in the dispersions, which provides a route to bespoke 3D enzyme plastic nanocomposite structures using a wide range of fabrication techniques, including melt electrowriting, casting, and piston-driven 3D printing. The resulting constructs comprising active phosphotriesterase (arPTE) readily detoxify organophosphates with persistent activity over repeated cycles and for long time periods. Moreover, we show that the protein guest molecules, such as arPTE or sfGFP, increase the compressive Young’s modulus of the plastics and that the identity of the biomolecule influences the nanomorphology and mechanical properties of the resulting materials. Overall, we demonstrate that these biologically active nanocomposite plastics are compatible with state-of-the-art 3D fabrication techniques and that the methodology could be readily applied to produce robust and on-demand smart nanomaterial structures.

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GB/T 7714-2015 [1] William H. Zhang, Graham J. Day, Ioannis Zampetakis, et al. ACS Applied Polymer Materials, 2021(3). DOI:10.1021/acsapm.1c00845.
MLA [1] William H. Zhang, et al., ACS Applied Polymer Materials, no. 3, 2021, https://doi.org/10.1021/acsapm.1c00845.
APA [1] William H. Zhang, Graham J. Day, Ioannis Zampetakis, Michele Carrabba, Zhongyang Zhang, Ben M. Carter, Norman Govan, Colin Jackson, Menglin Chen, & Adam W. Perriman. (2021). ACS Applied Polymer Materials(3). https://doi.org/10.1021/acsapm.1c00845
IEEE [1] William H. Zhang, Graham J. Day, Ioannis Zampetakis, Michele Carrabba, Zhongyang Zhang, Ben M. Carter, Norman Govan, Colin Jackson, Menglin Chen, and Adam W. Perriman, ACS Applied Polymer Materials, no. 3, 2021, doi: 10.1021/acsapm.1c00845. keywords: {nanocomposite;nanomorphology;functional bionanomaterials;enzyme;nanoconjugate;3D printing;melt electrowriting}