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基于生物相容性多糖多层膜的支撑脂质双层。

Supported lipid bilayers on biocompatible polysaccharide multilayers.

机构信息

Steacie Institute for Molecular Sciences, National Research Council of Canada, 100 Sussex Drive, Ottawa, Ontario, Canada K1A 0R6.

出版信息

Langmuir. 2011 Dec 6;27(23):14352-9. doi: 10.1021/la203207p. Epub 2011 Nov 9.

DOI:10.1021/la203207p
PMID:22013993
Abstract

Formation of supported lipid bilayers on soft polymer cushions is a useful approach to decouple the membrane from the substrate for applications involving membrane proteins. We prepared biocompatible polymer cushions by the layer-by-layer assembly of two polysaccharide polyelectrolytes, chitosan (CHI) and hyaluronic acid, on glass and silicon substrates. (CHI/HA)(5) films were characterized by atomic force microscopy, giving an average thickness of 57 nm and roughness of 25 nm in aqueous solution at pH 6.5. Formation of zwitterionic lipid bilayers by the vesicle fusion method was attempted using DOPC vesicles at pH 4 and 6.5 on (CHI/HA)(5) films. At higher pH adsorbed lipids had low mobility and large immobile lipid fractions; a combination of fluorescence and AFM indicated that this was attributable to formation of poor quality membranes with defects and pinned lipids rather than to a layer of surface-adsorbed vesicles. By contrast, more uniform bilayers with mobile lipids were produced at pH 4. Fluorescence recovery after photobleaching gave diffusion coefficients that were similar to those for bilayers on PEG cushions and considerably higher than those measured on other polyelectrolyte films. The results suggest that the polymer surface charge is more important than the surface roughness in controlling formation of mobile supported bilayers. These results demonstrate that polysaccharides provide a useful alternative to other polymer cushions, particularly for applications where biocompatibility is important.

摘要

在软聚合物垫上形成支撑脂质双层是一种将膜与基底分离的有用方法,适用于涉及膜蛋白的应用。我们通过在玻璃和硅衬底上层层组装两种多糖聚电解质壳聚糖(CHI)和透明质酸来制备生物相容性聚合物垫。(CHI/HA)(5)薄膜通过原子力显微镜进行了表征,在 pH 6.5 的水溶液中,其平均厚度为 57nm,粗糙度为 25nm。通过囊泡融合法尝试在(CHI/HA)(5)薄膜上用 DOPC 囊泡在 pH 4 和 6.5 下形成两性离子脂质双层。在较高的 pH 值下,吸附的脂质流动性低,不流动的脂质分数较大;荧光和 AFM 的组合表明,这归因于形成具有缺陷和固定脂质的质量较差的膜,而不是表面吸附囊泡的层。相比之下,在 pH 4 下形成了具有流动性脂质的更均匀的双层。光漂白后的荧光恢复给出了与 PEG 垫上的双层相似的扩散系数,明显高于在其他聚电解质薄膜上测量的值。结果表明,聚合物表面电荷比表面粗糙度更能控制流动性支撑双层的形成。这些结果表明,多糖为其他聚合物垫提供了一种有用的替代物,特别是在生物相容性很重要的应用中。

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