Bergman A, Dallner G
Biochim Biophys Acta. 1978 Sep 11;512(1):123-35. doi: 10.1016/0005-2736(78)90223-7.
Rough and smooth microsomes and Golgi membranes incorporate N-acetylglucosamine from UDP-N-acetylglucosamine into endogenous protein acceptors. A lipid intermediate of the dolichol phosphate type participates in this transfer reaction in the case of both microsomal subfractions, but the nature of lipid glycosylation is different in these two fractions. Glucosamine transfer in Golgi membranes does not appear to involve a lipid intermediate. In contrast to the results obtained under in vivo conditions, no glucosamine label is recovered in nascent ribosomal proteins or on luminal secretory proteins after incubation in vitro. Proteolysis of intact vesicles of the subfractions removes glycosylated dolichol phosphate and protein acceptors to various extents and interferes with transferase activities. This finding suggests the possiblity that glycosylation at the cytoplasmic side of the membrane of the endoplasmic reticulum may involve a system separate from that acting at the luminal side of the same membrane.
糙面微粒体、滑面微粒体和高尔基体膜能将来自尿苷二磷酸-N-乙酰葡糖胺的N-乙酰葡糖胺掺入内源性蛋白质受体中。对于这两种微粒体亚组分而言,磷酸多萜醇类型的脂质中间体参与了此转移反应,但在这两个组分中脂质糖基化的性质有所不同。高尔基体膜中的葡糖胺转移似乎不涉及脂质中间体。与体内条件下获得的结果相反,体外孵育后,新生核糖体蛋白或腔内分泌蛋白中未检测到葡糖胺标记。亚组分完整囊泡的蛋白水解会不同程度地去除糖基化的磷酸多萜醇和蛋白质受体,并干扰转移酶活性。这一发现表明,内质网膜胞质侧的糖基化可能涉及一个与同一膜腔侧作用的系统不同的系统。