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

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
出处
期刊:Science and Technology of Advanced Materials [Taylor & Francis]
卷期号:17 (1): 677-684 被引量:40
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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