Nanomaterials · 2019 · 13 citations · 33 references
Life SciencesBiochemistryBiologyMagnetic MaterialsNanomaterialsVirologyViral AssemblyViral HepatitisViral InfectionsViral StructureVirus MorphologyVirus-like NanoparticlesIron Oxide NanoparticlesNanoparticle Surface FunctionalizationSelf-assembling NanoparticlesStructural VirologyVirus-like Particle AssemblyVirus-like Particle MorphologyVirus-like Particle Self-assemblyVirus-like Particles
Core-virus like particles (VLPs) assembly is a kinetically complex cascade of interactions between viral proteins, nanoparticle’s surface and an ionic environment. Despite many in silico simulations regarding this process, there is still a lack of experimental data. The main goal of this study was to investigate the capsid protein of hepatitis B virus (HBc) assembly into virus-like particles with superparamagnetic iron oxide nanoparticles (SPIONs) as a magnetic core in relation to their characteristics. The native form of HBc was obtained via agroinfection of Nicotiana benthamiana with pEAQ-HBc plasmid. SPIONs of diameter of 15 nm were synthesized and functionalized with two ligands, providing variety in ζ-potential and hydrodynamic diameter. The antigenic potential of the assembled core-VLPs was assessed with enzyme-linked immunosorbent assay (ELISA). Morphology of SPIONs and core-VLPs was evaluated via transmission electron microscopy (TEM). The most successful core-VLPs assembly was obtained for SPIONs functionalized with dihexadecyl phosphate (DHP) at SPIONs/HBc ratio of 0.2/0.05 mg/mL. ELISA results indicate significant decrease of antigenicity concomitant with core-VLPs assembly. In summary, this study provides an experimental assessment of the crucial parameters guiding SPION-HBc VLPs assembly and evaluates the antigenicity of the obtained structures.
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Bernhard Schöpf, Heinrich Hofmann, Margarete Hofmann et al. · Journal of Magnetism and Magnetic Materials · 2005 · 1.7K citations · Full text
Hepatitis B: The virus and disease #
Jake T. Liang · Hepatology · 2009 · 1.1K citations · Full text
Biological Containers: Protein Cages as Multifunctional Nanoplatforms
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