Cho C S, Goto M, Kobayashi A, Kobayashi K, Akaike T
Department of Polymer Engineering, Chonnam National University, Kwangju, Korea.
J Biomater Sci Polym Ed. 1996;7(12):1097-104. doi: 10.1163/156856296x00589.
The orientation effect of galactose ligand on hepatocyte attachment was investigated. Poly(N-p-vinylbenzyl-o-beta-D-galactopyranosyl-D-gluconamide )(PVLA), a beta-galactose-carrying styrene homopolymer, was used as a model ligand for the asialoglycoprotein receptors on hepatocytes. PVLA was transferred onto the poly(gamma-benzyl L-glutamate) (PBLG) or PBLG/poly(ethylene glycol) (PEG)PBLG Langmuir-Blodgett (LB) films as the monolayer level. The dichroic fluorescence values of the confocal microscope indicated that the PVLA transferred onto the LB films was located with a preferential orientation of its molecular axes with regard to the direction of the alpha-helix of polypeptide. Hepatocyte recognized well-oriented galactose moieties of the surface of PVLA through asialoglycoprotein receptors.
研究了半乳糖配体对肝细胞附着的取向效应。聚(N-对乙烯基苄基-O-β-D-吡喃半乳糖基-D-葡糖酰胺)(PVLA),一种携带β-半乳糖的苯乙烯均聚物,被用作肝细胞上脱唾液酸糖蛋白受体的模型配体。PVLA以单层水平转移到聚(γ-苄基-L-谷氨酸)(PBLG)或PBLG/聚(乙二醇)(PEG)-PBLG朗缪尔-布洛杰特(LB)膜上。共聚焦显微镜的二向色荧光值表明,转移到LB膜上的PVLA的分子轴相对于多肽的α-螺旋方向具有优先取向。肝细胞通过脱唾液酸糖蛋白受体很好地识别了PVLA表面取向良好的半乳糖部分。