FURTHER FRACTIONATION OF THE GLYCOPROTEIN FAMILIES OF PORCINE ZONA PELLUCIDA BY ANION-EXCHANGE HPLC AND SOME CHARACTERIZATION OF THE SEPARATED FRACTIONS

被引:38
作者
NAKANO, M
HATANAKA, Y
KOBAYASHI, N
NOGUCHI, S
ISHIKAWA, S
TOBITA, T
机构
[1] Department of Chemiatry, Faculty of Science, Chiba University, Chiba
关键词
D O I
10.1093/oxfordjournals.jbchem.a122998
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 glycoproteins of porcine zonae pellucidae have been fractionated into three families (PZP1-3) by gel filtration HPLC [Nakano et al (1987) Biochem. InL 14,417-423]. However, they still comprize heterogeneous molecular species differing in electric charge. We found that sulfate, but not phosphate, is contained in PZP1-3 by a simple and rapid method for microanalysis of the anionic groups. These families were efficiently separated into many fractions by anion-exchange HPLC. When elution was performed by stepwise increase in NaCl concentration in 8 M urea/20 mM Tris-HCl, pH 8.0, a single distinctive peak emerged for each step. The analyses of amino acids, monosaccharides, and anions of the eight separated fractions of the major family, PZP3, showed that larger amounts of sulfated lactosamine linked to the constituent proteins are present in the fractions that are eluted later: the chain length and/or the chain number of these polylactosamines and the sulfate content increased with stepwise increase in NaCl concentration. Composition analyses also revealed that twice as much 7V-glycolylneuraminic acid is present as iV-acetylneuraminic acid in all fractions. The contents of these sialic acids in the fractions slightly increased in the order of elution. These results together with those of the analyses of endo-β-galactosidase digests showed that the charge heterogeneity of the porcine zona proteins is due mainly to differences in the amount of sulfated lactosamine, which is predominantly distributed in the non-reducing regions of the sugar chains. © 1990 COPYRIGHT, 1990 BY THE JOURNAL OF BIOCHEMISTRY.
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页码:144 / 150
页数:7
相关论文
共 39 条
[1]   STRUCTURE AND FUNCTION OF THE ZONA PELLUCIDA - IDENTIFICATION AND CHARACTERIZATION OF THE PROTEINS OF THE MOUSE OOCYTES ZONA PELLUCIDA [J].
BLEIL, JD ;
WASSARMAN, PM .
DEVELOPMENTAL BIOLOGY, 1980, 76 (01) :185-202
[2]   MAMMALIAN SPERM-EGG INTERACTION - FERTILIZATION OF MOUSE EGGS TRIGGERS MODIFICATION OF THE MAJOR ZONA PELLUCIDA GLYCOPROTEIN, ZP2 [J].
BLEIL, JD ;
BEALL, CF ;
WASSARMAN, PM .
DEVELOPMENTAL BIOLOGY, 1981, 86 (01) :189-197
[3]   MAMMALIAN SPERM-EGG INTERACTION - IDENTIFICATION OF A GLYCOPROTEIN IN MOUSE EGG ZONAE PELLUCIDAE POSSESSING RECEPTOR ACTIVITY FOR SPERM [J].
BLEIL, JD ;
WASSARMAN, PM .
CELL, 1980, 20 (03) :873-882
[4]   ROLE FOR FUCOSE-SULFATE-RICH CARBOHYDRATES IN THE PENETRATION OF ZONA-PELLUCIDA-FREE HAMSTER EGGS BY HAMSTER SPERMATOZOA [J].
DRAVLAND, JE ;
MORTIMER, D .
GAMETE RESEARCH, 1988, 21 (04) :353-358
[5]  
DUNBAR BS, 1981, BIOL REPROD, V24, P1111
[6]   STUDIES ON STRUCTURE OF HEPARIN [J].
DURANT, GJ ;
MONTGOMERY, R ;
HENDRICKSON, HR .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1962, 99 (03) :418-+
[7]   DEGLYCOSYLATION OF GLYCOPROTEINS BY TRIFLUOROMETHANESULFONIC ACID [J].
EDGE, ASB ;
FALTYNEK, CR ;
HOF, L ;
REICHERT, LE ;
WEBER, P .
ANALYTICAL BIOCHEMISTRY, 1981, 118 (01) :131-137
[8]   MEMBRANE DIFFERENTIATION IN HUMAN ERYTHROID-CELLS - UNIQUE PROFILES OF CELL-SURFACE GLYCOPROTEINS EXPRESSED IN ERYTHROBLASTS INVITRO FROM 3 ONTOGENIC STAGES [J].
FUKUDA, M ;
FUKUDA, MN ;
PAPAYANNOPOULOU, T ;
HAKOMORI, SI .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (06) :3474-3478
[9]   SPECTROFLUORIMETRIC DETERMINATION OF INORGANIC ANIONS - A REVIEW [J].
GOMEZHENS, A ;
VALCARCEL, M .
ANALYST, 1982, 107 (1274) :465-494
[10]   MOUSE EGG EXTRACELLULAR COAT IS A MATRIX OF INTERCONNECTED FILAMENTS POSSESSING A STRUCTURAL REPEAT [J].
GREVE, JM ;
WASSARMAN, PM .
JOURNAL OF MOLECULAR BIOLOGY, 1985, 181 (02) :253-264