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PNAS Plus: Lipid domains control myelin basic protein adsorption and membrane interactions between model myelin lipid bilayers

机译:PNAS Plus:脂质结构域控制髓磷脂基础蛋白的吸附以及模型髓磷脂脂质双层之间的膜相互作用

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摘要

The surface forces apparatus and atomic force microscope were used to study the effects of lipid composition and concentrations of myelin basic protein (MBP) on the structure of model lipid bilayers, as well as the interaction forces and adhesion between them. The lipid bilayers had a lipid composition characteristic of the cytoplasmic leaflets of myelin from “normal” (healthy) and “disease-like” [experimental allergic encephalomyelitis (EAE)] animals. They showed significant differences in the adsorption mechanism of MBP. MBP adsorbs on normal bilayers to form a compact film (3–4 nm) with strong intermembrane adhesion (∼0.36 mJ/m2), in contrast to its formation of thicker (7–8 nm) swelled films with weaker intermembrane adhesion (∼0.13 mJ/m2) on EAE bilayers. MBP preferentially adsorbs to liquid-disordered submicron domains within the lipid membranes, attributed to hydrophobic attractions. These results show a direct connection between the lipid composition of membranes and membrane–protein adsorption mechanisms that affects intermembrane spacing and adhesion and has direct implications for demyelinating diseases.
机译:用表面力仪器和原子力显微镜研究脂质成分和髓鞘碱性蛋白(MBP)浓度对模型脂质双层结构的影响,以及它们之间的相互作用力和粘附力。脂质双层具有来自“正常”(健康)和“疾病样” [实验性变应性脑脊髓炎(EAE)]动物的髓磷脂细胞质小叶的脂质组成特征。它们在MBP的吸附机理上显示出显着差异。 MBP吸附在正常的双层膜上,形成紧密膜(3-4 nm),其膜间附着力强(〜0.36 mJ / m 2 ),而形成的膜厚(7-8 nm)则膨胀膜在EAE双层上的膜间粘附力较弱(〜0.13 mJ / m 2 )。 MBP优先吸附到脂质膜中的液体无序亚微米域,这归因于疏水性吸引力。这些结果表明,膜的脂质组成与膜蛋白吸附机制之间存在直接联系,后者影响膜间的间隔和粘附,并直接影响脱髓鞘疾病。

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