SOB3, a human sperm protein involved in zona pellucida binding:: Physiological and biochemical analysis, purification

被引:0
作者
Ruiz, CM
Duquenne, C
Treton, D
Lefèvre, A
Finaz, C
机构
[1] Inst Federat Rech Cytokines, INSERM, U355, F-92140 Clamart, France
[2] Inst Federat Rech Cytokines, INSERM, U131, Clamart, France
关键词
fertilization; recognition protein; secondary binding;
D O I
10.1002/(SICI)1098-2795(199803)49:3<286::AID-MRD9>3.3.CO;2-#
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
LB5 antibody was selected from a monoclonal antibody (mAb) library directed against human sperm proteins. LB5 mAb detected the corresponding protein SOB3 in the neck region and the flagellum of most live ejaculated sperm while it labelled, in addition, the acrosome of about 10-20% of spermatozoa. The percentage of LB5 acrosome-stained sperm was significantly correlated with the percentages of either spontaneous or A23187-induced acrosome-reacted sperm. While SOB3 could not be detected in the testis, it appeared in spermatozoa from the corpus epididymis segment. LB5 mAb impaired neither sperm motion parameters, acrosomal reaction triggering, nor sperm binding to zona-free hamster oocytes. By contrast, LB5 Fab fragments (200 mu g/ml) inhibited sperm binding to human zonae pellicidae by 35.7%. If sperm were induced to acrosome react with A23187 prior to LB5 treatment, the inhibitory effect shifted to 59.9%, while no significant effect was observed following A23187 incubation alone. Western blotting of human sperm and cauda epididymis extracts revealed two bands of 18 and 19 kDa. While no cross-reaction was observed with other tested organs, a similar 18-kDa band was revealed in erythocytes and one of 19 kDa in B-lymphocytes. No cross-reactivity could be evidenced in any animal sperm analyzed. SOB3 was first separated in a 17- to 20-kDa preparative electrophoresis fraction and finally purified by isoelectrofocusing according to its pi of 9.8. These results suggest that SOB3 is localized under the outer acrosomal membrane, that it participates in secondary sperm binding to the zona pellucida, and that it shares homologies with the immune system. (C) 1998 Wiley-Liss, Inc.
引用
收藏
页码:286 / 297
页数:12
相关论文
共 47 条
[1]   MATURATION OF GUINEA-PIG SPERM IN THE EPIDIDYMIS INVOLVES THE MODIFICATION OF PROACROSIN OLIGOSACCHARIDE SIDE-CHAINS [J].
ANAKWE, OO ;
SHARMA, S ;
HOFF, HB ;
HARDY, DM ;
GERTON, GL .
MOLECULAR REPRODUCTION AND DEVELOPMENT, 1991, 29 (03) :294-301
[2]  
BABA T, 1994, J BIOL CHEM, V269, P31845
[3]   IDENTIFICATION OF A SECONDARY SPERM RECEPTOR IN THE MOUSE EGG ZONA PELLUCIDA - ROLE IN MAINTENANCE OF BINDING OF ACROSOME-REACTED SPERM TO EGGS [J].
BLEIL, JD ;
GREVE, JM ;
WASSARMAN, PM .
DEVELOPMENTAL BIOLOGY, 1988, 128 (02) :376-385
[4]   TISSUE-SPECIFIC AND SPECIES-SPECIFIC EXPRESSION OF SP56, A MOUSE SPERM FERTILIZATION PROTEIN [J].
BOOKBINDER, LH ;
CHENG, A ;
BLEIL, JD .
SCIENCE, 1995, 269 (5220) :86-89
[5]   Cases of human infertility are associated with the absence of P34H, an epididymal sperm antigen [J].
Boue, F ;
Sullivan, R .
BIOLOGY OF REPRODUCTION, 1996, 54 (05) :1018-1024
[6]   FLB1, A HUMAN PROTEIN OF EPIDIDYMAL ORIGIN THAT IS INVOLVED IN THE SPERM-OOCYTE RECOGNITION PROCESS [J].
BOUE, F ;
DUQUENNE, C ;
LASSALLE, B ;
LEFEVRE, A ;
FINAZ, C .
BIOLOGY OF REPRODUCTION, 1995, 52 (02) :267-278
[7]   HUMAN SPERM PROTEINS FROM TESTICULAR AND EPIDIDYMAL ORIGIN THAT PARTICIPATE IN FERTILIZATION - MODULATION OF SPERM BINDING TO ZONA-FREE HAMSTER OOCYTES, USING MONOCLONAL-ANTIBODIES [J].
BOUE, F ;
LASSALLE, B ;
DUQUENNE, C ;
VILLAROYA, S ;
TESTART, J ;
LEFEVRE, A ;
FINAZ, C .
MOLECULAR REPRODUCTION AND DEVELOPMENT, 1992, 33 (04) :470-480
[8]   INTERACTION OF A TYROSINE KINASE FROM HUMAN SPERM WITH THE ZONA-PELLUCIDA AT FERTILIZATION [J].
BURKS, DJ ;
CARBALLADA, R ;
MOORE, HDM ;
SALING, PM .
SCIENCE, 1995, 269 (5220) :83-86
[9]  
CERVONI F, 1992, J IMMUNOL, V148, P1431
[10]  
CERVONI F, 1993, J IMMUNOL, V151, P939