Tellechea Malda, EdurneAsensio, Aarón C.Ciáurriz Gortari, PaulaBuezo Bravo, JavierLópez Gómez, PedroUrra Rodríguez, MarinaMorán Juez, José Fernando2023-04-122023-04-122022Tellechea, E., Asensio, A. C., Ciaurriz, P., Buezo, J., López-Gómez, P., Urra, M., & Moran, J. F. (2022). A study of the interface of gold nanoparticles conjugated to cowpea fe-superoxide dismutase. Antioxidants, 11(11), 2082. https://doi.org/10.3390/antiox111120822076-392110.3390/antiox11112082https://academica-e.unavarra.es/handle/2454/45098The iron superoxide dismutase (FeSOD) is a first barrier to defend photosynthetic organisms from superoxide radicals. Although it is broadly present in plants and bacteria, FeSODs are absent in animals. They belong to the same phylogenic family as Mn-containing SODs, which are also highly efficient at detoxifying superoxide radicals. In addition, SODs can react with peroxynitrite, and FeSOD enzyme has already been used to evaluate the anti-nitrative capacity of plant antioxidants. Gold nanoparticles (AuNPs) have been shown to significantly improve the functionality and the efficiency of ligands, providing they are properly assembled. In this work, the characteristics of the recombinant cowpea (Vigna unguiculata) FeSOD (rVuFeSOD) immobilized onto AuNPs were investigated as a function of (1) NP surface chemistry and (2) biofunctionalization methods, either physical adsorption or covalent bonding. The NP surface chemistry was studied by varying the concentration of the ligand molecule 11-mercaptoundecanoic acid (MUA) on the NP surface. The coverage and activity of the protein on AuNPs was determined and correlated to the surface chemistry and the two biofunctionalization methods. rVuFeSOD–AuNPs conjugate stability was monitored through absorption measurements, agarose gel electrophoresis and DLS, enzymatic activity by a colorimetric assay and by in-gel activity assay, and coverage was measured by colorimetric assay. When using physical adsorption, the NP is the most perturbing agent for the activity of the enzyme. In contrast, only the NP coverage was affected by MUA ligand concentration. However, during covalent attachment, both the NP and the concentration of MUA on the surface influenced the enzyme activity, while the coverage of the NP remained constant. The results evidence the importance of the biomolecule and AuNP interaction for the functionality of the hybrid. These strategies can be used to develop electrochemical biosensors for O2•− and for peroxynitrite in biomedical applications.application/pdfeng© 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license.BiofunctionalizationGold nanoparticleSODSuperoxide dismutaseArtículo / Artikulua2023-04-12Acceso abierto / Sarbide irekiainfo:eu-repo/semantics/openAccess