| Texto completo | |
| Autor(es): |
Machado, Andre Campos
;
da Silva, Tamiris Reissa Cipriano
;
Raminelli, Cristiano
;
Caseli, Luciano
Número total de Autores: 4
|
| Tipo de documento: | Artigo Científico |
| Fonte: | Biophysical Chemistry; v. 293, p. 8-pg., 2022-12-23. |
| Resumo | |
Knowing how a bioactive compound interacts with cell membranes is important to understand its effect at the molecular level. In this sense, this work aimed to study the interaction of lysicamine, an alkaloid with action against lung cancer cell lines, with lipid monolayers as cell membrane models. We employed two lipid mixtures: the first composed of 35% DOPC, 30% DOPE, 20% sphingomyelin, and 15% cholesterol as healthy cell membranes models (MM1), and the second replacing DOPC with DOPS as cancer cells models (MM2). The interaction of lysicamine with the monolayers was evaluated using tensiometry, Brewster angle microscopy (BAM), and polarization-modulated infrared reflection-absorption spectroscopy (PM-IRRAS). Lysicamine had interfacial effects in both membrane models. For MM 1, it expanded the lipid monolayer and changed the interfacial rheological properties, increasing the in-plane elasticity of the films. PM-IRRAS spectra suggested a higher conformational disorder of the alkyl chains of the lipids. For MM 2, lysicamine also shifted the isotherms to higher areas, expanding the monolayers, but with no significant alteration in their interfacial rheological properties. PM-IRRAS spectra also suggested higher disorder in the orientation of the lipid alkyl chains upon lysicamine incorporation. For both models, BAM did not show alteration in interfacial aggregation upon drug incorporation. In conclusion, changes in some interfacial properties of membrane models caused by lysicamine depend on the monolayer composition, which can be associated with its bioactivity in cellular membranes. (AU) | |
| Processo FAPESP: | 20/01183-5 - Interação da lisicamina com modelos de membrana celular na interface ar-água |
| Beneficiário: | André Campos Machado |
| Modalidade de apoio: | Bolsas no Brasil - Mestrado |
| Processo FAPESP: | 20/12530-8 - 2-(Trimetilsilil)aril trifluorometanossulfonatos como precursores de arinos visando à preparação de compostos (hetero)aromáticos funcionalizados e sínteses de produtos naturais bioativos |
| Beneficiário: | Cristiano Raminelli |
| Modalidade de apoio: | Auxílio à Pesquisa - Regular |
| Processo FAPESP: | 18/22214-6 - Rumo à convergência de tecnologias: de sensores e biossensores à visualização de informação e aprendizado de máquina para análise de dados em diagnóstico clínico |
| Beneficiário: | Osvaldo Novais de Oliveira Junior |
| Modalidade de apoio: | Auxílio à Pesquisa - Temático |
| Processo FAPESP: | 22/03736-7 - Estudos sobre a interação de compostos bioativos em modelos de biointerface e construção de dispositivos nanoestruturados bioinspirados |
| Beneficiário: | Luciano Caseli |
| Modalidade de apoio: | Auxílio à Pesquisa - Regular |