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膜不对称性。

Membrane asymmetry.

作者信息

Rothman J E, Lenard J

出版信息

Science. 1977 Feb 25;195(4280):743-53. doi: 10.1126/science.402030.

Abstract

The components of biological membranes are asymmetrically distributed between the membrane surfaces. Proteins are absolutely asymmetrical in that every copy of a polypeptide chain has the same orientation in the membrane, and lipids are nonabsolutely asymmetrical in that almost every type of lipid is present on both sides of the bilayer, but in different and highly variable amounts. Asymmetry is maintained by lack of transmembrane diffusion. Two types of membrane proteins, called ectoproteins and endoproteins, are distinguished. Biosynthetic pathways for both types of proteins and for membrane lipids are inferred from their topography and distribution in the formed cells. Note added in proof. A cell-free system has now been developed which permits the mechanisms of membrane protein assembly to be studied (108). The membrane glycoprotein of vesicular stomatitis virus has been synthesized by wheat germ ribosomes in the presence of rough endoplasmic reticulum from pancreas. The resulting polypeptide is incorporated into the membrane, spans the lipid bilayer asymmetrically, and is glycosylated (108). The amino terminal portion of this transmembrane protein is found inside the endoplasmic reticulum vesicle, while the carboxyl terminal portion is exposed on the outer surface of the vesicle. Furthermore, addition of the glycoprotein to membranes after protein synthesis does not result in incorporation of the protein into the membrane in the manner described above (108). Consequently, protein synthesis and incorporation into the membrane must be closely coupled. Indeed, using techniques to synchronize the growth of nascent polypeptides, it has been shown (109) that no more than one-fourth of the glycoprotein chain can be made in the absence of membranes and still cross the lipid bilayer when chains are subsequently completed in the presence of membranes. These findings demonstrate directly that the extracytoplasmic portion of an ectoprotein can cross the membrane only during biosynthesis, and not after.

摘要

生物膜的成分在膜表面之间呈不对称分布。蛋白质是绝对不对称的,因为多肽链的每个拷贝在膜中都具有相同的取向,而脂质是非绝对不对称的,因为几乎每种脂质都存在于双层的两侧,但数量不同且变化很大。不对称性通过跨膜扩散的缺乏得以维持。区分出两种类型的膜蛋白,即外蛋白和内蛋白。从它们在形成细胞中的拓扑结构和分布推断出这两种类型蛋白质以及膜脂的生物合成途径。校样附注。现已开发出一种无细胞系统,可用于研究膜蛋白组装机制(108)。水泡性口炎病毒的膜糖蛋白已由小麦胚芽核糖体在胰腺糙面内质网存在的情况下合成。产生的多肽被整合到膜中,不对称地跨越脂质双层,并进行糖基化(108)。这种跨膜蛋白的氨基末端部分位于内质网囊泡内部,而羧基末端部分暴露在囊泡的外表面。此外,在蛋白质合成后将糖蛋白添加到膜中不会导致蛋白质以上述方式整合到膜中(108)。因此,蛋白质合成和整合到膜中必须紧密耦合。实际上,使用使新生多肽生长同步的技术已表明(109),在没有膜的情况下合成的糖蛋白链不超过四分之一,并且当随后在有膜的情况下完成链的合成时,仍能穿过脂质双层。这些发现直接证明,外蛋白的胞外部分只能在生物合成过程中穿过膜,而不能在之后穿过。

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