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Internalization and Cellular Fate of Protein Corona-Coated Nanoparticles by Multimodal Multi-Scale Microscopy

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Autor(es):
Galdino, Flavia E. ; Rabelo, Renata S. ; Scarpa, Isabella ; Yoneda, Juliana S. ; Consonni, Silvio R. ; Leme, Adriana F. Paes ; Smith, Andrew M. ; Harkiolaki, Maria ; Cardoso, Mateus B.
Número total de Autores: 9
Tipo de documento: Artigo Científico
Fonte: SMALL; v. N/A, p. 11-pg., 2024-12-08.
Resumo

Upon exposure to biological environments, nanoparticles are rapidly coated with biomolecules, predominantly proteins, which alter their colloidal stability, biodistribution, and cell interactions. Despite extensive efforts to investigate the nanoparticles' fate, only a few studies use high-resolution characterization methods that allow in-depth characterization, and the existing methodologies are unable to differentiate particles internalized at the onset of incubation from those taken up toward the end of an incubation period. In this study, these limitations related to incubation disparities are overcame and precisely monitored the spatiotemporal displacement of colloidally stable protein corona-coated nanoparticles within cells. An unprecedented application of cryogenic X-ray nanotomography, combined with high-resolution, super-resolution, and correlative microscopy techniques, revealed the migration of nanoparticles to the perinuclear region while monitoring the evolution of cellular organelles in fully hydrated cells under near-native conditions, without the need for contrasting agents. Notably, this tracking indicates the progressive fusion of vesicles carrying the nanoparticles intracellularly. This strategy demonstrates the potential for uncovering the temporal aspects of nanoparticle behavior within cells and can be adaptable to a wide range of nanoparticles and cell types, offering a versatile and powerful tool to follow nanoparticles in cellular environments. (AU)

Processo FAPESP: 18/09555-9 - Estudo da influência da proteina corona na interação e internalização de nanopartículas de sílica em células humanas: do imageamento bidimensional ao tridimensional
Beneficiário:Flávia Elisa Galdino
Modalidade de apoio: Bolsas no Brasil - Doutorado
Processo FAPESP: 21/12071-6 - Arquitetando coloides via interações supramoleculares: de fundamentos a aplicações
Beneficiário:Watson Loh
Modalidade de apoio: Auxílio à Pesquisa - Temático
Processo FAPESP: 19/00720-0 - Impacto da adsorção de proteínas na localização de nanopartículas dentro de células de mamífero
Beneficiário:Mateus Borba Cardoso
Modalidade de apoio: Auxílio à Pesquisa - Regular