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Interaction of poly(ethylene glycol)-conjugated phospholipids with supported lipid membranes and their influence on protein adsorption

机译:聚乙二醇共轭磷脂与脂质膜的相互作用及其对蛋白质吸附的影响

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摘要

We studied real-time interaction between poly(ethylene glycol)-conjugated phospholipids (PEG-lipids) and a supported lipid membrane by surface plasmon resonance (SPR) spectroscopy to understand dynamic behaviors of PEG-lipids on living cell membranes. Supported lipid membranes formed on a hydrophobic surface were employed as a model of living cell membrane. We prepared three kinds of PEG-lipids that carried alkyl chains of different lengths for SPR measurements and also performed fluorescence recovery after photobleaching (FRAP) to study the influence of acyl chain length on dynamics on the supported membrane. PEG-lipids were uniformly anchored to lipid membranes with high fluidity without clustering. Incorporation and dissociation rates of PEG-lipids into supported membranes strongly depended on the length of acyl chains; longer acyl chains reduced the incorporation rate and the dissociation rate of PEG-lipid. Furthermore, protein adsorption experiment with bovine serum albumin indicated that PEG modification prevented the adsorption of bovine serum albumin on such supported membrane.
机译:我们通过表面等离振子共振(SPR)光谱研究了聚(乙二醇)共轭磷脂(PEG-脂质)和支持的脂质膜之间的实时相互作用,以了解PEG-脂质在活细胞膜上的动态行为。在疏水表面上形成的支撑脂质膜被用作活细胞膜的模型。我们制备了三种带有不同长度烷基链的PEG-脂质,用于SPR测量,还进行了光漂白(FRAP)后的荧光恢复,以研究酰基链长度对负载膜动力学的影响。 PEG-脂质以高流动性均匀地锚定在脂质膜上,而不会聚集。 PEG-脂质在支持膜中的结合和解离速率很大程度上取决于酰基链的长度。较长的酰基链会降低PEG-脂质的掺入率和解离速率。此外,牛血清白蛋白的蛋白质吸附实验表明,PEG修饰阻止了牛血清白蛋白在这种支持的膜上的吸附。

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