首页> 美国卫生研究院文献>Journal of Visualized Experiments : JoVE >Detergent-free Ultrafast Reconstitution of Membrane Proteins into Lipid Bilayers Using Fusogenic Complementary-charged Proteoliposomes.
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Detergent-free Ultrafast Reconstitution of Membrane Proteins into Lipid Bilayers Using Fusogenic Complementary-charged Proteoliposomes.

机译:使用融合的互补电荷蛋白脂质体将无蛋白的膜蛋白无洗涤剂超快重建为脂质双层。

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摘要

Detergents are indispensable for delivery of membrane proteins into 30-100 nm small unilamellar vesicles, while more complex, larger model lipid bilayers are less compatible with detergents.Here we describe a strategy for bypassing this fundamental limitation using fusogenic oppositely charged liposomes bearing a membrane protein of interest. Fusion between such vesicles occurs within 5 min in a low ionic strength buffer. Positively charged fusogenic liposomes can be used as simple shuttle vectors for detergent-free delivery of membrane proteins into biomimetic target lipid bilayers, which are negatively charged. We also show how to reconstitute membrane proteins into fusogenic proteoliposomes with a fast 30-min protocol.Combining these two approaches, we demonstrate a fast assembly of an electron transport chain consisting of two membrane proteins from E. coli, a primary proton pump bo3-oxidase and F1Fo ATP synthase, in membranes of vesicles of various sizes, ranging from 0.1 to >10 microns, as well as ATP production by this chain.
机译:清洁剂对于将膜蛋白递送到30-100 nm的单层小囊泡中是必不可少的,而更复杂,较大的模型脂质双层则与去污剂的相容性较低。在此,我们描述了一种使用带有膜蛋白的反向融合带负电荷的脂质体绕过这一基本限制的策略。出于兴趣。这些囊泡之间的融合在5分钟内在低离子强度缓冲液中发生。带正电荷的融合脂质体可以用作简单的穿梭载体,用于将膜蛋白无洗涤剂地递送至带负电荷的仿生目标脂质双层中。我们还展示了如何通过30分钟的快速流程将膜蛋白重构为融合蛋白脂质体。结合这两种方法,我们展示了由两种膜蛋白(主要来自质子泵bo3-)从大肠杆菌中快速组装的电子传输链。大小介于0.1至> 10微米的囊泡膜中的氧化酶和F1Fo ATP合酶以及由该链产生的ATP。

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