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哺乳动物糖蛋白的生物合成。非还原末端序列合成中的糖基化途径。

Biosynthesis of mammalian glycoproteins. Glycosylation pathways in the synthesis of the nonreducing terminal sequences.

作者信息

Beyer T A, Rearick J I, Paulson J C, Prieels J P, Sadler J E, Hill R L

出版信息

J Biol Chem. 1979 Dec 25;254(24):12531-4.

PMID:500730
Abstract

Six purified glycosyltransferase (a beta-galactoside alpha 2 leads to 6 sialyltransferase, a beta-galactoside alpha 2 leads to 3 sialyltransferase, an alpha-N-acetylgalactosaminide alpha 2 leads to 6 sialyltransferase, a beta-galactoside alpha 1 leads to 2 fucosyltransferase, a beta-N-acetylglucosaminide alpha 1 leads to 3 fucosyltransferase, and a (fucosyl alpha 1 leads to 2) galactoside alpha 1 leads to 3 N-acetyl-galactosaminyltransferase) have been used to study the biosynthetic pathways for formation of the nonreducing terminal oligosaccharide sequences in mammalian glycoproteins. The two glycoproteins used as model acceptor substrates in this study were human asialotransferrin, which contains the nonreducing terminal oligosaccharide sequence Gal beta 1 leads to 4GlcNAc beta 1 leads to 2Man, and antifreeze glycoprotein, which contains oligosaccarides with the structure, Gal beta 1 leads to 3GalNAc alph 1 leads O-Thr. Sequential action of the six glycosyltransferases on these model substrates led to the formation of previously described oligosaccharide structures. The studies reported here indicate that the substrate specificities of the individual enzymes dictate the structures that can be synthesized and the pathways by which they may be formed. The actions of a number of the transferasesare mutually exclusive, thereby prohibiting the formation of theoretically possible oligosaccharide structures. Oligosaccharides with the terminal sequence NeuAc alpha 2 leads to 3(Fuc alpha 1 leads to 2)Gal beta 1 leads to 3GalNAc and NeuAc alpha 2 leads to 6Gal beta 1 leads to 4(Fuc alpha 1 leads to 3)GlcNAc cannot be formed because the prior incorporation of sialic acid by the sialyltransferases yields products that are not acceptor substrates for the fucosyltransferases, and vice versa. Synthesis of other products requires that the enzymes act sequentially in a specific order. The structures NeuAc alpha 2 leads to 6(Fuc alpha 1 leads to 2)Gal beta 1 leads to 4GlcNAc, Fuc alpha 1 leads to 2Gal beta 1 leads to 4(Fuc alpha 1 leads to 3)GlcNAc, GalNAc alpha 1 leads to 3(Fuc alpha 1 leads to 2)Gal beta 1 leads to 4GlcNAc, and GalNAc alpha 1 leads to 3(Fuc alpha 1 leads to 2)Gal beta 1 leads to 3GalNAc can only be synthesized if the fucosyl alpha 1 leads to 2 galactose linkage is formed first. Synthesis of the pentasaccharide sequences GalNAc alpha 1 leads to 3(Fuc alpha 1 leads to 2)Gal beta 1 leads to 3(NeuAc alpha 2 leads to 6)GalNAc and GalNAc alpha 1 leads to 3(Fuc alpha 1 leads to 2)Gal beta 1 leads to 4(Fuc alpha 1 leads to 3)GlcNAc requires that the N-acetylgalactosaminyltransferase act last on the former structure and that the alpha 1 leads to 3 fucosyltransferase act last on the latter. In those instances where a product can be formed by one of two possible pathways, the comparisons of reaction rates indicate that one pathway is usually preferred...

摘要

六种纯化的糖基转移酶(一种β-半乳糖苷α2→6唾液酸转移酶、一种β-半乳糖苷α2→3唾液酸转移酶、一种α-N-乙酰半乳糖胺α2→6唾液酸转移酶、一种β-半乳糖苷α1→2岩藻糖基转移酶、一种β-N-乙酰葡糖胺α1→3岩藻糖基转移酶和一种(岩藻糖基α1→2)半乳糖苷α1→3 N-乙酰半乳糖胺基转移酶)已被用于研究哺乳动物糖蛋白中非还原末端寡糖序列形成的生物合成途径。本研究中用作模型受体底物的两种糖蛋白是人去唾液酸转铁蛋白,其含有非还原末端寡糖序列Galβ1→4GlcNAcβ1→2Man,以及抗冻糖蛋白,其含有结构为Galβ1→3GalNAcα1→O-Thr的寡糖。六种糖基转移酶对这些模型底物的顺序作用导致了先前描述的寡糖结构的形成。此处报道的研究表明,各个酶的底物特异性决定了可以合成的结构以及它们可能形成的途径。许多转移酶的作用是相互排斥的,从而阻止了理论上可能的寡糖结构的形成。具有末端序列NeuAcα2→3(Fucα1→2)Galβ1→3GalNAc和NeuAcα2→6Galβ1→4(Fucα1→3)GlcNAc的寡糖无法形成,因为唾液酸转移酶预先掺入唾液酸会产生不是岩藻糖基转移酶受体底物的产物,反之亦然。其他产物的合成要求酶按特定顺序依次作用。结构NeuAcα2→6(Fucα1→2)Galβ1→4GlcNAc、Fucα1→2Galβ1→4(Fucα1→3)GlcNAc、GalNAcα1→3(Fucα1→2)Galβ1→4GlcNAc和GalNAcα1→3(Fucα1→2)Galβ1→3GalNAc只有在首先形成岩藻糖基α1→2半乳糖连接时才能合成。五糖序列GalNAcα1→3(Fucα1→2)Galβ1→3(NeuAcα2→6)GalNAc和GalNAcα1→3(Fucα1→2)Galβ1→4(Fucα1→3)GlcNAc的合成要求N-乙酰半乳糖胺基转移酶最后作用于前一种结构,而α1→3岩藻糖基转移酶最后作用于后一种结构。在一种产物可以通过两种可能途径之一形成的那些情况下,反应速率的比较表明通常优先选择一种途径……

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