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Formation of three-dimensional protein-lipid aggregates in monolayer films induced by surfactant protein B.

机译:表面活性剂蛋白B诱导的单层膜中三维蛋白质-脂质聚集体的形成。

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摘要

This study focuses on the structural organization of surfactant protein B (SP-B) containing lipid monolayers. The artificial system is composed of the saturated phospholipids dipalmitoylphosphatidylcholine (DPPC) and dipalmitoylphosphatidylglycerol (DPPG) in a molar ratio of 4:1 with 0.2 mol% SP-B. The different "squeeze-out" structures of SP-B were visualized by scanning probe microscopy and compared with structures formed by SP-C. Particularly, the morphology and material properties of mixed monolayers containing 0.2 mol% SP-B in a wide pressure range of 10 to 54 mN/m were investigated revealing that filamentous domain boundaries occur at intermediate surface pressure (15-30 mN/m), while disc-like protrusions prevail at elevated pressure (50-54 mN/m). In contrast, SP-C containing lipid monolayers exhibit large flat protrusions composed of stacked bilayers in the plateau region (app. 52 mN/m) of the pressure-area isotherm. By using different scanning probe techniques (lateral force microscopy, force modulation, phase imaging) it was shown that SP-B is dissolved in the liquid expanded rather than in the liquid condensed phase of the monolayer. Although artificial, the investigation of this system contributes to further understanding of the function of lung surfactant in the alveolus.
机译:这项研究的重点是表面活性剂蛋白B(SP-B)包含脂质单层的结构组织。人工系统由饱和磷脂二棕榈酰磷脂酰胆碱(DPPC)和二棕榈酰磷脂酰甘油(DPPG)与0.2 mol%SP-B的摩尔比为4:1组成。通过扫描探针显微镜观察SP-B的不同“挤出”结构,并将其与SP-C形成的结构进行比较。特别是,在10至54 mN / m的宽压力范围内,研究了含有0.2 mol%SP-B的混合单层的形态和材料性能,发现在中间表面压力(15-30 mN / m)处出现丝状畴边界,碟形突起在较高压力(50-54 mN / m)时占优势。相反,含SP-C的脂质单分子层在压力区域等温线的稳定区域(约52 mN / m)中显示出由堆叠的双层构成的大的平坦突起。通过使用不同的扫描探针技术(横向力显微镜,力调制,相成像),表明SP-B溶解在膨胀的液体中,而不是溶解在单层的液体冷凝相中。虽然是人工的,但对该系统的研究有助于进一步了解肺表面活性剂在肺泡中的功能。

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