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Specific recognition of the lectine and adamantyl- glycoconjugates on liposome surface as artificial cell membrane


Štimac, Adela; Šegota, Suzana; Dutour Sikirić, Maja; Ribić, Rosana; Frkanec, Leo; Svetličić, Vesna; Tomić, Srđanka; Vranešić, Branka; Frkanec, Ruža
Specific recognition of the lectine and adamantyl- glycoconjugates on liposome surface as artificial cell membrane // Knjiga sažetaka, 23. Hrvatski skup kemičara i kemijskih inženjera / Hadžiev, Andrea ; Blažeković, Zdenko (ur.).
Osijek: HKDI/Kemija u industriji, 2013. str. 147-147 (poster, domaća recenzija, sažetak, znanstveni)


Naslov
Specific recognition of the lectine and adamantyl- glycoconjugates on liposome surface as artificial cell membrane

Autori
Štimac, Adela ; Šegota, Suzana ; Dutour Sikirić, Maja ; Ribić, Rosana ; Frkanec, Leo ; Svetličić, Vesna ; Tomić, Srđanka ; Vranešić, Branka ; Frkanec, Ruža

Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni

Izvornik
Knjiga sažetaka, 23. Hrvatski skup kemičara i kemijskih inženjera / Hadžiev, Andrea ; Blažeković, Zdenko - Osijek : HKDI/Kemija u industriji, 2013, 147-147

ISBN
978-953-6894-50-5

Skup
23. Hrvatski skup kemičara i kemijskih inženjera

Mjesto i datum
Osijek, Hrvatska, 21.-24.04.2013

Vrsta sudjelovanja
Poster

Vrsta recenzije
Domaća recenzija

Ključne riječi
Mannosylated adamantyl-glycoconjugates ; liposomes ; membrane ; recognition ; lectine

Sažetak
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.

Izvorni jezik
Engleski

Znanstvena područja
Kemija, Kemijsko inženjerstvo



POVEZANOST RADA


Projekt / tema
021-0212432-2431 - Nove formulacije antigena i imunostimulatora - utjecaj na imunoreakciju (Ruža Frkanec, )

Ustanove
Imunološki zavod d.d.,
Institut "Ruđer Bošković", Zagreb