Display of Recombinant Membrane Receptors on Giant Liposomes: Attempt to Construct a Cell Model with Integrated Membrane Protein Systems

K. Tsumoto, K. Kamiya, T. Yoshimura
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引用次数: 4

Abstract

Giant unilamellar vesicles (GUVs), or giant liposomes (GLs), are biochemical compartments enclosed with phospholipid bilayers. The size of GUVs is comparable to that of real cells (~10-100 mum). Thus, GUVs are employed to construct artificial cell models, which are reconstituted from biochemical materials to mimic real cellular functions in a simpler manner for investigation of fundamental mechanisms of living systems. However, transmembrane proteins are difficult to reconstitute on GUV bilayers. In order to obtain GUVs containing transmembrane proteins, giant proteoliposomes, here, we introduce the novel method using membrane fusion between GUVs and recombinant baculovirus (Autographa californica nucleopolyhedrovirus (AcNPV)). It is known that the AcNPV budded virus (BV) displays recombinant membrane proteins on their own envelopes. BVs have fusogenic envelope glycoproteins (gp64) sensitive to acidic pH. Combination of these two features may produce giant proteoliposomes. The fusion properties were observed using fluorescence microscopy to comprehend conditions suitable for reconstitution of proteoliposomes. The display of a 7-fold transmembrane receptor protein (G protein-coupled receptor) on GUVs was also demonstrated using fluoroimmuno microscopic observation.
重组膜受体在巨脂质体上的展示:构建整合膜蛋白系统的细胞模型的尝试
巨型单层囊泡(GUVs)或巨型脂质体(GLs)是由磷脂双层包裹的生化室。guv的大小与真实细胞相当(~10-100 μ m)。因此,guv被用于构建人工细胞模型,这些模型由生化材料重组,以更简单的方式模拟真实的细胞功能,用于研究生命系统的基本机制。然而,跨膜蛋白很难在GUV双分子层上重组。为了获得含有跨膜蛋白、巨蛋白脂质体的guv,本文介绍了guv与重组杆状病毒(加利福尼亚自签名核多角体病毒(AcNPV))膜融合的新方法。已知AcNPV出芽病毒(BV)在其自身的包膜上显示重组膜蛋白。bv具有对酸性ph敏感的融合性包膜糖蛋白(gp64),两者结合可产生巨大的蛋白脂质体。利用荧光显微镜观察融合特性,了解适合重组蛋白脂质体的条件。利用荧光免疫显微镜观察也证实了7倍跨膜受体蛋白(G蛋白偶联受体)在guv上的显示。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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