Specific recognition of the lectine and adamantyl- glycoconjugates on liposome surface as artificial cell membrane (CROSBI ID 597192)
Prilog sa skupa u zborniku | sažetak izlaganja sa skupa | domaća recenzija
Podaci o odgovornosti
Štimac, Adela ; Šegota, Suzana ; Dutour Sikirić, Maja ; Ribić, Rosana ; Frkanec, Leo ; Svetličić, Vesna ; Tomić, Srđanka ; Vranešić, Branka ; Frkanec, Ruža
engleski
Specific recognition of the lectine and adamantyl- glycoconjugates on liposome surface as artificial cell membrane
Mannosylated adamantyl-glycoconjugates, namely (2R)-N-(adamant-1-yl)-3-(a, b-D- mannopyranosyloxy)-2-methylpropanamide and (2R)-N- [3-(α-D-mannopyranosyloxy)-2-methylpropanoyl]-D, L- (adamant-2-yl)glycyl-L-alanyl-D-isoglutamine] were incorporated into liposomes and the surface of the liposome morphology was examined. In order to determine the entrapment efficiency, size, shape and surface changes on the liposomes, HPLC, dynamic light scattering (DLS) and atomic force microscopy (AFM) were used. We have previously shown the interaction of immunostimulating adamantyltripeptides and phospholipids in liposomal bilayers. Now, we were primarily interested to study incorporation profile of mannosylated adamantyl-glycoconjugates. We have demonstrated that the adamantyl moiety, due to its liphophilic properties, penetrates into the lipid core of the bilayer while the hydrophilic part with the mannosyl moiety is exposed on the liposome surface. After concanavalin A (Con A), a lectin, which specifically binds α-D-mannosyl residues, was added to the liposome preparation, increase in liposome size and appearance of aggregates has been observed. The enlargement of liposomes was ascribed to the specific binding of the Con A to the mannose present on the surface of the prepared vesicles. The AFM analysis revealed that the mannosylated 1- aminoadamantane molecules were evenly distributed in a lipid bilayer, while mannosylated adamantyltripeptide molecules grouped into small domains that raise above the bilayer surface. The molecule size and molecular geometry, as well as the hydrophilic and hydrophobic surfaces in the structure of mannosylated adamantylglycopeptides, are responsible for arrangement of molecules in the lipid bilayer. This approach might be a useful model for investigation of specific protein interactions with membrane receptors. Also, the adamantyl moiety may be considered as a potential membrane anchor for different carbohydrate or other molecules of interest, which could be bound on it and thus exposed on liposome surfaces and as such used in targeted drug delivery.
mannosylated adamantyl-glycoconjugates ; liposomes ; membrane ; recognition ; lectine
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Podaci o prilogu
147-147.
2013.
objavljeno
Podaci o matičnoj publikaciji
23. Hrvatski skup kemičara i kemijskih inženjera - knjiga sažetaka
Hadžiev, Andrea ; Blažeković, Zdenko
Osijek: Hrvatsko društvo kemijskih inženjera i tehnologa (HDKI)
978-953-6894-50-5
Podaci o skupu
23. HRVATSKI SKUP KEMIČARA I KEMIJSKIH INŽENJERA
poster
21.04.2013-24.04.2013
Osijek, Hrvatska