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A modular platform for one-step assembly of multi-component membrane systems by fusion of charged proteoliposomes

机译:通过融合带电蛋白脂质体一步组装多组分膜系统的模块化平台

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摘要

An important goal in synthetic biology is the assembly of biomimetic cell-like structures, which combine multiple biological components in synthetic lipid vesicles. A key limiting assembly step is the incorporation of membrane proteins into the lipid bilayer of the vesicles. Here we present a simple method for delivery of membrane proteins into a lipid bilayer within 5 min. Fusogenic proteoliposomes, containing charged lipids and membrane proteins, fuse with oppositely charged bilayers, with no requirement for detergent or fusion-promoting proteins, and deliver large, fragile membrane protein complexes into the target bilayers. We demonstrate the feasibility of our method by assembling a minimal electron transport chain capable of adenosine triphosphate (ATP) synthesis, combining Escherichia coli F1Fo ATP-synthase and the primary proton pump bo3-oxidase, into synthetic lipid vesicles with sizes ranging from 100 nm to ∼10 μm. This provides a platform for the combination of multiple sets of membrane protein complexes into cell-like artificial structures.
机译:合成生物学的一个重要目标是仿生细胞样结构的组装,该结构在合成脂质囊泡中结合了多种生物成分。关键的限制组装步骤是将膜蛋白掺入囊泡的脂质双层中。在这里,我们提出了一种在5分钟内将膜蛋白递送到脂质双层中的简单方法。融合的蛋白脂质体,包含带电荷的脂质和膜蛋白,与带相反电荷的双层融合,不需要去污剂或融合促进蛋白,并将大而易碎的膜蛋白复合物输送到目标双层中。我们通过将能够合成三磷酸腺苷(ATP)的最小电子传输链组装在一起,将大肠杆菌F1Fo ATP合酶和主要质子泵bo3-氧化酶组合成大小从100 nm至〜10μm。这提供了将多组膜蛋白复合物组合成细胞样人工结构的平台。

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