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首页> 外文期刊>Colloids and Surfaces, B. Biointerfaces >Interactions between single-chained ether phospholipids and sphingomyelin in mixed monolayers at the air/water interface-Grazing incidence X-ray diffraction and Brewster angle microscopy studies
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Interactions between single-chained ether phospholipids and sphingomyelin in mixed monolayers at the air/water interface-Grazing incidence X-ray diffraction and Brewster angle microscopy studies

机译:空气/水界面混合单层中单链醚磷脂和鞘磷脂之间的相互作用-掠入射X射线衍射和Brewster角显微镜研究

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摘要

Single-chained ether phospholipids comprise a class of both natural (PAF, lyso-PAF) and synthetic (edelfosine, ED) compounds possessing confirmed extensive biological activities. Among them ED is known to exhibit antineoplastic properties, while PAF and its lyso-precursor are lipids implicated e.g. in the functioning of organism immune system. In our study the interactions of ED, PAF and lyso-PAF with sphingomyelin (SM) being one of the main lipid found in a high concentration in membrane microdomains, like lipid rafts, were investigated in mixed monolayers at the air/water interface. The traditional Langmuir methodology was complemented with modern physicochemical techniques: Grazing incidence X-ray diffraction and Brewster angle microscopy. The investigated compounds, i.e.: platelet activating factor (PAF), (lyso-PAF) and edelfosine were selected because of their highly different physiological properties despite very similar chemical structure and evidenced membrane activity. The obtained results demonstrate that all the investigated three single-chained phospholipids cause strong modification of the model membrane properties in a concentration dependent manner. It has been proved that there are significant differences regarding the influence of the single-chained lipids on model SM membrane - in the region of low concentration, edelfosine was found to be the most effective among all the investigated compounds. The collected data shed new light onto the membrane behavior of the investigated herein biochemically active compounds, which can be of help in understanding their different biological activity and designing of new, more biocompatible drugs.
机译:单链醚磷脂既包含天然化合物(PAF,溶血PAF),也包含合成化合物(edelfosine,ED),具有广泛的生物活性。其中已知ED表现出抗肿瘤性质,而PAF及其溶菌前体是涉及脂质,例如。在机体免疫系统的功能。在我们的研究中,ED,PAF和溶血PAF与鞘磷脂(SM)的相互作用是在膜微域(如脂质筏)中高浓度发现的主要脂质之一,在空气/水界面的混合单层中进行了研究。传统的朗格缪尔方法与现代的物理化学技术相辅相成:放牧入射X射线衍射和布儒斯特角显微镜。选择了所研究的化合物,即:血小板活化因子(PAF),(溶血PAF)和依德福星,因为它们的生理特性差异很大,尽管它们的化学结构非常相似并且具有明显的膜活性。获得的结果表明,所有研究的三种单链磷脂均以浓度依赖性方式引起模型膜性质的强烈修饰。已经证明,关于单链脂质对模型SM膜的影响存在显着差异-在低浓度区域,发现在所有研究的化合物中,依地芬新最有效。收集的数据为本文研究的生物化学活性化合物的膜行为提供了新的思路,这有助于理解它们的不同生物活性以及设计新的,更具生物相容性的药物。

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