膜
乙二醇
PEG比率
蛋白质吸附
化学
牛血清白蛋白
吸附
膜流动性
烷基
共轭体系
生物物理学
有机化学
色谱法
生物化学
聚合物
生物
财务
经济
作者
Toshihiro Yamamoto,Yuji Teramura,Toru Itagaki,Yusuke Arima,Hiroo Iwata
标识
DOI:10.1080/14686996.2016.1240006
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.
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