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Scanning force microscopy at the air-water interface of an air bubble coated with pulmonary surfactant.

机译:在涂有肺表面活性剂的气泡的空气-水界面处的扫描力显微镜检查。

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摘要

To study the structure-function relationship of pulmonary surfactant under conditions close to nature, molecular films of a model system consisting of dipalmitoylphosphatidylcholine, dipalmitoylphosphatidylglycerol, and surfactant-associated protein C were prepared at the air-water interface of air bubbles about the size of human alveoli (diameter of 100 microm). The high mechanical stability as well as the absence of substantial film flow, inherent to small air bubbles, allowed for scanning force microscopy (SFM) directly at the air-water interface. The SFM topographical structure was correlated to the local distribution of fluorescent-labeled dipalmitoylphosphatidylcholine, as revealed from fluorescence light microscopy of the same bubbles. Although SFM has proven before to be exceptionally well suited to probe the structure of molecular films of pulmonary surfactant, the films so far had to be transferred onto a solid support from the air-water interface of a film balance, where they had been formed. This made them prone to artifacts imposed by the transfer. Moreover, the supported monolayers disallowed the direct observation of the structural dynamics associated with expansion and compression of the films as upon breathing. The current findings are compared in this respect to our earlier findings from films, transferred onto a solid support.
机译:为了研究在接近自然的条件下肺表面活性剂的结构-功能关系,在大约与人大小相近的气泡的空气-水界面处制备了由二棕榈酰磷脂酰胆碱,二棕榈酰磷脂酰甘油和表面活性剂相关蛋白C组成的模型系统的分子膜。肺泡(直径为100微米)。高机械稳定性以及小气泡所固有的不存在大量薄膜流动的特性,使得扫描力显微镜(SFM)可以直接在空气-水界面处进行。从相同气泡的荧光显微镜显示,SFM的地形结构与荧光标记的二棕榈酰磷脂酰胆碱的局部分布有关。尽管之前已证明SFM非常适合探测肺表面活性剂分子膜的结构,但迄今为止,这些膜必须从形成膜的天平的空气-水界面转移到固体支持物上。这使他们容易受到转让造成的伪影。而且,被支撑的单分子层不允许直接观察与呼吸时薄膜的膨胀和压缩有关的结构动力学。在这方面,将当前的发现与我们先前从电影中获得的发现进行比较,并将其转移到坚实的支持物上。

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