The role of human lysozyme-like protein 4 in fertilization and its enzymatic properties.
- Author:
Peng HUANG
1
;
Neng QIAN
2
;
Wang-Chun DU
1
;
Wei-Jun SHI
1
;
Qing-Wen SUN
3
;
Ning ZHANG
2
Author Information
1. School of Clinical Medicine, Shanghai College of Medical and Health Sciences, Shanghai 201318, China.
2. School of Basic Medicine, Shanghai College of Medical and Health Sciences, Shanghai 201318, China.
3. School of Life Sciences, Fudan University, Shanghai 200438, China.
- Publication Type:Journal Article
- Keywords:
acrosome;
free radical;
hyaluronan;
sperm-egg binding;
human lysozyme-like protein 4
- MeSH:
Acrosome;
enzymology;
Animals;
Blotting, Western;
Cricetinae;
Enzyme-Linked Immunosorbent Assay;
Epididymis;
Female;
Fertilization;
physiology;
Free Radical Scavengers;
metabolism;
Humans;
Hyaluronic Acid;
metabolism;
Male;
Muramidase;
analysis;
physiology;
Pichia;
Plasmids;
metabolism;
Recombinant Proteins;
analysis;
metabolism;
Sperm-Ovum Interactions;
physiology;
Spermatozoa;
enzymology;
Testis
- From:National Journal of Andrology
2018;24(2):109-115
- CountryChina
- Language:Chinese
-
Abstract:
Objective:To elucidate the possible role of human lysozyme-like protein 4 (LYZL4) in fertilization and characterize its enzymatic properties.
METHODS:The localization of LYZL4 in human spermatozoa was investigated by immunofluorescence staining, the sources of LYZL4 on the sperm surface examined by RT-PCR, and the role of LYZL4 in fertilization assessed by the zona-free hamster egg penetration test. The recombinant plasmid pPIC9K-LYZL4 was constructed and its expression induced with methanol after transformed into competent Pichia pastoris GS115. The recombinant LYZL4 protein (rLYZL4) was purified from the fermentation supernatant and subsequently identified by Western blot. The hyaluronan binding ability of rLYZL4 was determined by ELISA and the muramidase activity, hyaluronidase activity, and free radical scavenging ability examined by spectrophotometric methods.
RESULTS:Immunodetection with a specific antiserum localized LYZL4 on the acrosomal membrane of mature spermatozoa, which was exclusively secreted from the testis and epididymis as shown by RT-PCR. Immunoneutralization of LYZL4 significantly decreased the number of human spermatozoa bound to zona-free hamster eggs in a dose-dependent manner in vitro. The recombinant protein was expressed successfully by the P. pastoris strain GS115. Purified rLYZL4 exhibited a potent hyaluronan binding ability and a strong free radical scavenging ability but no muramidase or hyaluronidase activity.
CONCLUSIONS:LYZL4 secreted from the testis and epididymis is localized on the acrosomal membrane of mature spermatozoa and plays a role in sperm-egg binding as well as in binding hyaluronan and scavenging free radicals, which suggests that it might be a multi-functional molecule contributive to sperm protection and sperm-egg binding.
