Abstract

Plant viruses are perfect candidates for the construction of nanobiotechnological devices. When employed in intricate 2D or 3D architectures, a stable, ordered virus layer, as the foundational plane, is a prerequisite. In former investigations, Coulomb‐force‐assisted self‐assembly is utilized. However, these layers demonstrate instability in further processing in a solution. In this study, an innovative strategy for immobilizing tomato bushy stunt viral (TBSV) nanoparticles through specific binding is reported on. Genetically engineered TBSV nanoparticles with Strep‐Tag II side chains are anchored using surface‐immobilized Strep‐Tactin. Strep‐Tactin, an engineered type of streptavidin with a strong specific interaction with the Strep‐Tag II protein, is immobilized on a silicon wafer through 3‐aminopropyltriethoxyilane and maleimide functionalization. Herein, the investigation involves optimizing the viral concentration and the pH values of the viral solution, facilitating the achievement of an optimal distribution of viral nanoparticles without vacancies during immobilization. The Strep‐Tactin/Strep‐Tag II system significantly improves the coverage of viral particles on the silicon substrate compared to the direct immobilization onto the untreated silicon substrate. The formed layers exhibit remarkable stability, even under sonication. To validate the findings, scanning force microscopy serves as a critical tool for imaging.

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