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ACS Appl Mater Interfaces ; 16(28): 37248-37254, 2024 Jul 17.
Article in English | MEDLINE | ID: mdl-38957146

ABSTRACT

Gas cluster ion beam (GCIB)-assisted deposition is used to build multilayered protein-based structures. In this process, Ar3000-5000+ clusters bombard and sputter molecules from a reservoir (target) to a collector, an operation that can be sequentially repeated with multiple targets. The process occurs under a vacuum, making it adequate for further sample conservation in the dry state, since many proteins do not have long-term storage stability in the aqueous state. First of all, the stability in time and versatility in terms of molecule selection are demonstrated with the fabrication of peptide multilayers featuring a clear separation. Then, lysozyme and trypsin are used as protein models to show that the activity remaining on the collector after deposition is linearly proportional to the argon ion dose. The energy per atom (E/n) of the Ar clusters is a parameter that was also changed for lysozyme deposition, and its increase negatively affects activity. The intact detection of larger protein molecules by SDS-PAGE gel electrophoresis and a bioassay (trypsin at ≈25 kDa and glucose oxidase (GOx) at ≈80 kDa) is demonstrated. Finally, GOx and horseradish peroxidase, two proteins involved in the same enzymatic cascade, are successively deposited on ß-d-glucose to build an on-demand release material in which the enzymes and the substrate (ß-d-glucose) are combined in a dry trilayer, and the reaction occurs only upon reintroduction in aqueous medium.


Subject(s)
Glucose Oxidase , Horseradish Peroxidase , Muramidase , Trypsin , Muramidase/chemistry , Muramidase/metabolism , Glucose Oxidase/chemistry , Glucose Oxidase/metabolism , Trypsin/chemistry , Trypsin/metabolism , Horseradish Peroxidase/chemistry , Horseradish Peroxidase/metabolism , Peptides/chemistry , Animals , Glucose/chemistry
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