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Controlled shaping of lipid vesicles in a microfluidic diffusion chamber

机译:微流体扩散室中脂质囊泡的受控整形

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摘要

Synthetic lipid vesicles represent an important model system for studying membrane processes, which often depend on membrane shape, but controlled shaping of vesicles remains a challenging experimental task. Here, we present a novel method for shaping giant lipid vesicles by independently regulating osmotic conditions and the concentration of membrane-shaping molecules, which intercalate into the membrane and drive membrane bending. The method is based on the microfluidic diffusion chamber, where the solution around the vesicles can be repeatedly exchanged solely by diffusion, without any hydrodynamic flow that could deform the membrane. By using lipopolysaccharide (LPS) as a vesicle shape-modifying molecule, we demonstrate controlled and reversible transformations across three shape classes, from invaginated to evaginated vesicles. We show that extensive shape transformations can lead to shapes that are assumed to comprise narrow membrane necks that hinder equilibration of the membrane and the vesicle interior. All the observed shapes are in good agreement with the predictions of the area-difference-elasticity model applied to the vesicles that were denser than their surrounding solution. Our results validate the microfluidic diffusion chamber as a universal framework for membrane shaping that could also pave the way towards controlled fabrication of synthetic membranes resembling cell-compartments with large surface-to-volume ratios.
机译:合成脂质囊泡是研究膜过程的重要模型系统,膜过程通常取决于膜形状,但囊泡的受控整形仍然是一项具有挑战性的实验任务。在这里,我们提出了一种通过独立调节渗透条件和膜成形分子浓度来塑造巨型脂质囊泡的新方法,这些分子插入膜并驱动膜弯曲。该方法基于微流体扩散室,其中囊泡周围的溶液可以仅通过扩散重复交换,而没有任何可能使膜变形的流体动力流。通过使用脂多糖 (LPS) 作为囊泡形状修饰分子,我们展示了从内陷到蒸发囊泡的三个形状类别的受控和可逆转化。我们表明,广泛的形状转变会导致假定包含狭窄的膜颈的形状,从而阻碍膜和囊泡内部的平衡。所有观察到的形状都与面积-差异-弹性模型的预测非常吻合,该模型应用于密度大于其周围溶液的囊泡。我们的研究结果验证了微流体扩散室作为膜成型的通用框架,这也可以为受控制造类似于具有大表面积比的细胞隔室的合成膜铺平道路。

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