| Autor: |
Batova I; Department of Obstetrics and Gynecology, Hyogo Medical College, Nishinomiya, Japan., Kameda K, Hasegawa A, Koyama K, Tsuji Y, Isojima S |
| Jazyk: |
angličtina |
| Zdroj: |
Journal of reproductive immunology [J Reprod Immunol] 1990 Mar; Vol. 17 (1), pp. 1-16. |
| DOI: |
10.1016/0165-0378(90)90035-5 |
| Abstrakt: |
A hybridoma (3B2-F7) has been established which secretes a monoclonal antibody (Mab) directed against a peptide determinant of human seminal plasma glycoprotein (HSP-gP). The deglycosylation of HSP-gP was performed chemically with TFMS hydrolysis and enzymatically in the presence of detergent and further treated with periodic acid after fixing deglycosylated HSP on plastic wells. The Mab 3B2-F7 (IgM, kappa) exhibited sperm immobilization activity (256 units of SI50) and inhibited sperm binding to human zona pellucida. Human epididymis, pancreatic islets of Langerhan's and distal tubulus of kidney were strongly labelled whilst other tissues were essentially negative by avidin-biotin complex tissue staining with this Mab. The antigen epitope to the Mab was in the 36 kDa molecule of human HSP-gP. The antigenic determinant recognized by Mab 3B2-F7 was destroyed by six different proteases, but was resistant to N-glycanase and other carbohydrate splitting enzymes. This epitope is therefore likely to be composed of a polypeptide chain. Peptide fragments after proteolysis of the HSP molecule with Staph. aureus V8 protease and trypsin retained antigenicity, hence the epitope corresponding to the Mab may be a peptide chain and not dependent on the conformational structure of the polypeptide. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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