Optimizing the Stability of Viral Nanoparticles: Engineering Strategies, Applications, and the Emerging Concept of the Virophore.

Nanoparticles derived from plant viruses and bacteriophages are self-assembling structures that can be functionalized for broad applications in drug delivery, vaccine formulation, and imaging, as well as the engineering of nanomaterials, and nanoscale templating. Their capacity for precise chemical and genetic modification makes them versatile, but their functional potential may be limited by insufficient or poorly controlled structural stability. In this perspectives article, we assess recent advances in stability optimization to improve the functionality of virus-based nanoparticles and derived materials, considering engineering strategies that target the external and internal surfaces, as well as the interfaces between coat protein subunits. We look at approaches such as site-specific bioconjugation, reversible and permanent cross-linking, polymer endoskeleton reinforcement, metal ion coordination, and protective core-shell architectures, which can be used to tailor particle stability for harsh biological environments, or create particles with responsive stability profiles allowing smart delivery systems to release cargo when exposed to triggers such as pH, redox potential, illumination, or mechanical stress. We propose the concept of the virophore: a genetically or chemically encoded functional unit integrated into the structure of a virus particle that acts as a programmable structural switch, enabling reversible, triggerable reconfiguration in response to defined stimuli. We argue that embracing virophore design will expand the capabilities of virus-based nanomaterials beyond passive durability, facilitating adaptive, intelligent behavior. This will support applications such as programmable drug release, biosensors, and dynamic material systems.

Duke Scholars

Author Stephen L Craig Chemistry