Comparison of the N-linked glycans from soluble and GPI-anchored CD59 expressed in CHO cells

被引:19
作者
Wheeler, SF
Rudd, PM
Davis, SJ
Dwek, RA
Harvey, DJ
机构
[1] Univ Oxford, Dept Biochem, Oxford Glycobiol Inst, Oxford OX1 3QU, England
[2] Univ Oxford, Nuffield Dept Clin Med, Mol Sci Div, Oxford OX3 9DU, England
关键词
CD59; CHO cells; MALDI MS; N-acetyllactosamine extensions; N-linked glycosylation;
D O I
10.1093/glycob/12.4.261
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 tetraantermary 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-->4Fuc, 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.
引用
收藏
页码:261 / 271
页数:11
相关论文
共 45 条
  • [1] Export of a misprocessed GPI-anchored protein from the endoplasmic reticulum in vitro in an ATP- and cytosol-dependent manner
    Ali, BRS
    Claxton, S
    Field, MC
    [J]. FEBS LETTERS, 2000, 483 (01) : 32 - 36
  • [2] PRIMARY STRUCTURE OF N-LINKED CARBOHYDRATE CHAINS OF A HUMAN CHIMERIC PLASMINOGEN-ACTIVATOR K2TU-PA EXPRESSED IN CHINESE-HAMSTER OVARY CELLS
    BERGWERFF, AA
    VANOOSTRUM, J
    ASSELBERGS, FAM
    BURGI, R
    HOKKE, CH
    KAMERLING, JP
    VLIEGENTHART, JFG
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1993, 212 (03): : 639 - 656
  • [3] NONSELECTIVE AND EFFICIENT FLUORESCENT LABELING OF GLYCANS USING 2-AMINO BENZAMIDE AND ANTHRANILIC ACID
    BIGGE, JC
    PATEL, TP
    BRUCE, JA
    GOULDING, PN
    CHARLES, SM
    PAREKH, RB
    [J]. ANALYTICAL BIOCHEMISTRY, 1995, 230 (02) : 229 - 238
  • [4] Mutational analysis of the active site and antibody epitopes of the complement-inhibitory glycoprotein, CD59
    Bodian, DL
    Davis, SJ
    Morgan, BP
    Rushmere, NK
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 185 (03) : 507 - 516
  • [5] Neutral N-glycans in adult rat brain tissue - Complete characterisation reveals fucosylated hybrid and complex structures
    Chen, YJ
    Wing, DR
    Guile, GR
    Dwek, RA
    Harvey, DJ
    Zamze, S
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1998, 251 (03): : 691 - 703
  • [6] OLIGOSACCHARIDE STRUCTURES PRESENT ON ASPARAGINE-289 OF RECOMBINANT HUMAN PLASMINOGEN EXPRESSED IN A CHINESE-HAMSTER OVARY CELL-LINE
    DAVIDSON, DJ
    CASTELLINO, FJ
    [J]. BIOCHEMISTRY, 1991, 30 (03) : 625 - 633
  • [7] MEMBRANE DEFENSE AGAINST COMPLEMENT LYSIS - THE STRUCTURE AND BIOLOGICAL PROPERTIES OF CD59
    DAVIES, A
    LACHMANN, PJ
    [J]. IMMUNOLOGIC RESEARCH, 1993, 12 (03) : 258 - 275
  • [8] CD59, AN LY-6-LIKE PROTEIN EXPRESSED IN HUMAN LYMPHOID-CELLS, REGULATES THE ACTION OF THE COMPLEMENT MEMBRANE ATTACK COMPLEX ON HOMOLOGOUS CELLS
    DAVIES, A
    SIMMONS, DL
    HALE, G
    HARRISON, RA
    TIGHE, H
    LACHMANN, PJ
    WALDMANN, H
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1989, 170 (03) : 637 - 654
  • [9] The glycan processing and site occupancy of recombinant Thy-1 is markedly affected by the presence of a glycosylphosphatidylinositol anchor
    Devasahayam, M
    Catalino, PD
    Rudd, PM
    Dwek, RA
    Barclay, AN
    [J]. GLYCOBIOLOGY, 1999, 9 (12) : 1381 - 1387
  • [10] FUKUDA M, 1988, J BIOL CHEM, V263, P5314