Wheeler Susan F, Rudd Pauline M, Davis Simon J, Dwek Raymond A, Harvey David J
Oxford Glycobiology Institute, Department of Biochemistry, South Parks Road, Oxford, OX1 3QU, United Kingdom.
Glycobiology. 2002 Apr;12(4):261-71. doi: 10.1093/glycob/12.4.261.
The N-linked glycosylation of recombinant human CD59, expressed in Chinese hamster ovary (CHO) cells with and without a membrane anchor, was compared to examine the effect of the anchor on glycan processing. N-Linked glycans were released with peptide-N-glycosidase F (PNGase F) within gel from SDS-PAGE-isolated soluble and glycosylphosphatidylinositol (GPI)-anchored human CD59 expressed in CHO cells. The anchored form contained core-fucosylated neutral and sialylated bi-, tri-, and tetraantennary glycans with up to four N-acetyllactosamine extensions. Exoglycosidase digestions and analysis by matrix-assisted laser desorption/ionization (MALDI) mass spectrometry were used to define the relative amounts of the bi-, tri-, and tetraantennary glycans and to investigate the distribution of N-acetyllactosamine extensions between their antennae. Biantennary structures accounted for about 60% of the glycans, 30% of the triantennary structures, and about 10% of the tetraantennary structures. For tri- and tetraantennary glycans, those with extended antennae were found to be more abundant than those without extensions. The soluble form of CD59, expressed in CHO cells without the GPI anchor signal sequence, consisted almost entirely (97%) of biantennary glycans, of which 81% were unmodified, 17% contained one N-acetyllactosamine extension, and 2% contained two extensions. No compounds with longer extensions were found. A MALDI spectrum of the intact glycoprotein showed a distribution of glycans that matched those released with PNGase F. In addition, the protein was substituted with several small glycans, such as HexNAc, HexNAc-->Fuc, and HexNAc-->HexNAc, probably as the result of degradation of the mature N-linked glycans. The results show that the presence of the anchor increases the extent of glycan processing, possibly as the result of longer exposure to the glycosyltransferases or to a closer proximity of the protein to these enzymes.
比较了在有或没有膜锚定的情况下,在中国仓鼠卵巢(CHO)细胞中表达的重组人CD59的N-连接糖基化,以研究锚定对聚糖加工的影响。通过肽-N-糖苷酶F(PNGase F)从SDS-PAGE分离的可溶性和糖基磷脂酰肌醇(GPI)锚定的、在CHO细胞中表达的人CD59凝胶内释放N-连接聚糖。锚定形式包含核心岩藻糖基化的中性和唾液酸化的二天线、三天线和四天线聚糖,带有多达四个N-乙酰乳糖胺延伸。使用外切糖苷酶消化和基质辅助激光解吸/电离(MALDI)质谱分析来确定二天线、三天线和四天线聚糖的相对含量,并研究N-乙酰乳糖胺延伸在其天线之间的分布。二天线结构约占聚糖的60%,三天线结构占30%,四天线结构约占10%。对于三天线和四天线聚糖,发现有延伸天线的比没有延伸的更丰富。在没有GPI锚定信号序列的CHO细胞中表达的CD59可溶性形式几乎完全(97%)由二天线聚糖组成,其中81%未修饰,17%含有一个N-乙酰乳糖胺延伸,2%含有两个延伸。未发现有更长延伸的化合物。完整糖蛋白的MALDI谱显示聚糖分布与用PNGase F释放的聚糖相匹配。此外,该蛋白被几种小聚糖取代,如己糖胺、己糖胺→岩藻糖和己糖胺→己糖胺,这可能是成熟N-连接聚糖降解的结果。结果表明,锚定的存在增加了聚糖加工的程度,这可能是由于与糖基转移酶接触时间更长或蛋白质与这些酶更接近的结果。