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高尔基体中的糖基化机制。

Mechanism of glycosylation in the Golgi apparatus.

作者信息

Fleischer B

出版信息

J Histochem Cytochem. 1983 Aug;31(8):1033-40. doi: 10.1177/31.8.6345657.

Abstract

A major role of the Golgi apparatus in liver is the terminal glycosylation of secreted serum proteins and of plasma membrane glycoproteins. Galactosyltransferase is a membrane-bound Golgi enzyme that transfers galactose directly from uridine diphosphogalactose (UDP-Gal) to terminal N-acetylglucosamine groups of N-asparagine-linked glycoproteins during secretion. Sialytransferase then transfers sialic acid from cytidine monophosphosialic acid (CMP-NAN) to the newly added terminal galactose of the glycoprotein. In the cell, the transfer reaction must occur on the lumen side of the Golgi membrane. UDP-Gal is synthesized mainly in the cytoplasm and CMP-NAN is synthesized in the nucleus in liver. An important question for understanding the mechanism is, how do these nucleotide sugars gain access to the transferases? A second question involves uridine diphosphate (UDP), a highly inhibitory product of galactosyltransferase. How is UDP removed from the lumen of the Golgi fast enough to prevent product inhibition of the galactosyltransferase? We have shown that isolated Golgi, although vesiculated, retains its original orientation. The vesicles are oriented with greater than 90% of both galactosyltransferase and sialyl-transferase on the luminal side of the vesicles. Using intact vesicles, we can show that UDP-Gal is taken up via a saturable carrier system present in the Golgi membrane. During galactosylation in vitro, UDP formed in the lumen of Golgi vesicles is rapidly converted to UMP by a nucleoside diphosphatase in the lumen. Uridine monophosphate, which is much less inhibitory to the galactosyltransferase than UDP, is then transported out of the lumen by a second carrier and is broken down further to uridine by 5'-nucleotidase on the cytoplasmic side of the Golgi vesicles. The transport of nucleotides appears unique to the Golgi membranes, since neither rough endoplasmic reticulum nor plasma membrane vesicles from rat liver accumulate these nucleotides.

摘要

高尔基体在肝脏中的一个主要作用是对分泌的血清蛋白和质膜糖蛋白进行终末糖基化。半乳糖基转移酶是一种膜结合的高尔基体酶,在分泌过程中,它将半乳糖从尿苷二磷酸半乳糖(UDP-Gal)直接转移到N-天冬酰胺连接的糖蛋白的末端N-乙酰葡糖胺基团上。然后唾液酸转移酶将胞苷单磷酸唾液酸(CMP-NAN)中的唾液酸转移到糖蛋白新添加的末端半乳糖上。在细胞中,转移反应必须发生在高尔基体膜的腔面。UDP-Gal主要在细胞质中合成,而CMP-NAN在肝脏的细胞核中合成。理解该机制的一个重要问题是,这些核苷酸糖是如何进入转移酶的?第二个问题涉及尿苷二磷酸(UDP),它是半乳糖基转移酶的一种高度抑制性产物。UDP是如何足够快地从高尔基体腔中去除,以防止对半乳糖基转移酶的产物抑制?我们已经表明,分离的高尔基体虽然形成了囊泡,但仍保持其原来的方向。囊泡的方向是,超过90%的半乳糖基转移酶和唾液酸转移酶位于囊泡的腔面。使用完整的囊泡,我们可以表明UDP-Gal是通过高尔基体膜中存在的一种可饱和载体系统摄取的。在体外半乳糖基化过程中,高尔基体囊泡腔中形成的UDP被腔中的核苷二磷酸酶迅速转化为UMP。尿苷单磷酸对半乳糖基转移酶的抑制作用比UDP小得多,然后通过第二种载体被转运出腔,并在高尔基体囊泡的细胞质侧被5'-核苷酸酶进一步分解为尿苷。核苷酸的转运似乎是高尔基体膜所特有的,因为来自大鼠肝脏的糙面内质网和质膜囊泡都不会积累这些核苷酸。

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