Abstract
The sperm receptor activity of pig zona pellucida has been previously shown to exist in one of the components, pig zona protein 3 alpha (PZP3 alpha), that can be purified after the removal of sialylated and/or sulfated N-acetylpoly(lactosamine) by digestion with endo-beta-galactosidase. In this study, we examined whether N-linked or O-linked carbohydrate chains are involved in the sperm receptor activity of pig zona pellucida. The elimination of N-linked carbohydrate chains from endo-beta-galactosidase-digested PZP3 alpha by digestion with N-glycanase markedly reduced its inhibitory effect on sperm-egg binding in an in vitro competition assay, whereas the elimination of O-linked carbohydrate chains by alkali treatment hardly reduced the inhibitory effect. These results indicate that N-linked carbohydrate chains of PZP3 alpha play a major role in mediating the sperm binding of zona pellucida in pig.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Amidohydrolases
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Animals
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Binding Sites
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Carbohydrate Metabolism*
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Carbohydrates / chemistry
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Carbohydrates / isolation & purification
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Egg Proteins / chemistry
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Egg Proteins / isolation & purification
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Egg Proteins / metabolism
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Female
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Glycoside Hydrolases*
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In Vitro Techniques
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Male
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Membrane Glycoproteins / chemistry
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Membrane Glycoproteins / isolation & purification
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Membrane Glycoproteins / metabolism
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Molecular Structure
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Peptide-N4-(N-acetyl-beta-glucosaminyl) Asparagine Amidase
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Receptors, Cell Surface / chemistry
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Receptors, Cell Surface / isolation & purification
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Receptors, Cell Surface / metabolism
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Sperm-Ovum Interactions / physiology*
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Spermatozoa / metabolism
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Swine
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Zona Pellucida / chemistry
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Zona Pellucida / metabolism*
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beta-Galactosidase
Substances
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Carbohydrates
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Egg Proteins
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Membrane Glycoproteins
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Receptors, Cell Surface
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egg surface sperm receptor
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Glycoside Hydrolases
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keratan-sulfate endo-1,4-beta-galactosidase
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beta-Galactosidase
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Amidohydrolases
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Peptide-N4-(N-acetyl-beta-glucosaminyl) Asparagine Amidase