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糖供体向糖基化位点的膜转运。

Membrane transport of sugar donors to the glycosylation sites.

作者信息

Verbert A, Cacan R, Cecchelli R

出版信息

Biochimie. 1987 Feb;69(2):91-9. doi: 10.1016/0300-9084(87)90240-9.

Abstract

The assembly of N-linked glycoproteins in eukaryotic cells begins with the segregation of these molecules within the lumen of intracellular vesicles. Since the sugar nucleotides are cytoplasmic molecules, translocation of the sugar moiety across the membrane appears as a crucial event in the glycoprotein synthesis. This N-glycosylation process occurs in two different cytological sites: in the rough endoplasmic reticulum, the stepwise synthesis of a large lipid-linked oligosaccharide takes place, as well as its transfer to protein; then after trimming the immature glycoprotein is further elongated in the Golgi apparatus. In this paper, a brief review will be given of the present knowledge on the sugar donor transport across the membrane barrier to the glycosylation site. Based upon the transmembrane orientation of oligosaccharide lipid intermediates and on the localization of the glycosyltransferase active sites, the different processes required to translocate the sugar moieties during the preassembly of the dolichyl-pyrophosphate-oligosaccharides will be examined. Combining the different results, obtained in several laboratories, it is suggested that the Man5-GlcNAc2-lipid is synthesized on the cytoplasmic side directly from the sugar-nucleotides and then translocated to the lumenal face where the Glc3-Man9-GlcNAc2-lipid is completed using Man-P-Dol and Glc-P-Dol as transmembrane carriers of these sugars. Concerning the elongation process leading to assembly of the antennae of N-acetyllactosamine type oligosaccharides, specific carriers for sugar nucleotides have been described as Golgi markers. Several authors have characterized such carriers for UDP-Gal, GDP-Fuc, CMP-NeuAc, UDP-GlcNAc and UDP-Glc using microsomal vesicles and similar results have been obtained in our laboratory using plasma membrane permeabilized cells. This carrier-mediated process leads to the formation of an intralumenal pool whose biological significance will be discussed. The translocation process of sugar donors occurring in the rough endoplasmic reticulum via lipid intermediates as well as in the Golgi apparatus via specific carriers would represent a regulation step based on the availability of the substrates for the glycosylation.

摘要

真核细胞中N-连接糖蛋白的组装始于这些分子在细胞内囊泡腔中的分离。由于糖核苷酸是细胞质分子,糖部分跨膜转运似乎是糖蛋白合成中的关键事件。这种N-糖基化过程发生在两个不同的细胞学部位:在糙面内质网中,会进行一种大的脂质连接寡糖的逐步合成及其向蛋白质的转移;然后在修剪后,未成熟的糖蛋白在高尔基体中进一步延长。本文将简要回顾目前关于糖供体跨膜屏障转运至糖基化位点的知识。基于寡糖脂质中间体的跨膜方向以及糖基转移酶活性位点的定位,将研究在二磷酸多萜醇 - 寡糖预组装过程中转运糖部分所需的不同过程。综合几个实验室获得的不同结果,有人提出Man5-GlcNAc2-脂质在细胞质一侧直接由糖核苷酸合成,然后转运至腔面,在那里使用Man-P-Dol和Glc-P-Dol作为这些糖的跨膜载体完成Glc3-Man9-GlcNAc2-脂质的合成。关于导致N-乙酰乳糖胺型寡糖天线组装的延长过程,已描述了糖核苷酸的特定载体作为高尔基体标志物。几位作者使用微粒体囊泡对UDP-Gal、GDP-Fuc、CMP-NeuAc、UDP-GlcNAc和UDP-Glc的此类载体进行了表征,并且我们实验室使用质膜通透细胞也获得了类似结果。这种载体介导的过程导致形成一个腔内池,其生物学意义将予以讨论。糖供体通过脂质中间体在糙面内质网中以及通过特定载体在高尔基体中发生的转运过程可能代表基于糖基化底物可用性的调节步骤。

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