The Hinge Region of Bovine Zona Pellucida Glycoprotein ZP3 Is Involved in the Formation of the Sperm-Binding Active ZP3/ZP4 Complex

• Published in: Biomolecules (Basel, Switzerland) Switzerland), 2015-11, Vol.5 (4), p.3339-3353
• Main Authors: Suzuki, Kaori, Tatebe, Nanami, Kojima, Sayuri, Hamano, Ayumi, Orita, Misaki, Yonezawa, Naoto
• Format: Article
• Language: English
• Subjects: Amino Acid Sequence; Animals; baculovirus-Sf9 cell; Binding Sites; Cattle; Egg Proteins - chemistry; Egg Proteins - genetics; Egg Proteins - metabolism; fertilization; glycoprotein; Male; Membrane Glycoproteins - chemistry; Membrane Glycoproteins - genetics; Membrane Glycoproteins - metabolism; Molecular Sequence Data; Protein Binding; Receptors, Cell Surface - chemistry; Receptors, Cell Surface - genetics; Receptors, Cell Surface - metabolism; Sf9 Cells; Spermatozoa - metabolism; Spodoptera; zona pellucida; Zona Pellucida Glycoproteins
• ISSN: 2218-273X; 2218-273X
• DOI: 10.3390/biom5043339

The zona pellucida (ZP) surrounds the mammalian oocyte and mediates species-selective sperm-oocyte interactions. Bovine ZP consists of glycoproteins ZP2, ZP3, and ZP4. Neither ZP3 nor ZP4 alone shows inhibitory activity for the binding of sperm to the ZP; however, this activity is seen with the ZP3/ZP4 heterocomplex. Here, we constructed a series of bovine ZP3 mutants to identify the ZP4-binding site on ZP3. Each ZP3 mutant was co-expressed with ZP4 using a baculovirus-Sf9 cell expression system and examined for interaction with ZP4 as well as inhibitory activity for sperm-ZP binding. N-terminal fragment Arg-32 to Arg-160 of ZP3 interacted with ZP4 and inhibited sperm-ZP binding, whereas fragment Arg-32 to Thr-155 showed much weaker interaction with ZP4. Mutation of N-glycosylated Asn-146 to Asp in the N-terminal fragment Arg-32 to Glu-178 of ZP3 did not interrupt the interaction of this fragment with ZP4, but it did reduce the inhibitory activity of the complex for sperm-ZP binding. In contrast, mutation of N-glycosylated Asn-124 to Asp did not significantly reduce the activity. Taken together, these results suggest that one of the ZP4 binding sites exists in the flexible hinge region of ZP3 and that the N-glycosylation in this region is involved in the sperm binding.