Abstract
Fertilization in the sea urchin involves species-specific interaction between the ligand bindin on the surface of acrosome-reacted sperm and a receptor of high molecular weight on the surface of the egg. Efforts to understand this interaction and the resultant signal transduction events leading to egg activation have been limited because of the large size and extreme insolubility of the intact receptor on the egg surface. Earlier work suggested that an alternative strategy would be to isolate proteolytic fragments of the extracellular domain of this receptor. Consequently, we have treated S. purpuratus eggs with a specific protease, lysylendoproteinase C. This enzyme treatment abolished the ability of eggs to bind sperm and resulted in the release of proteolytic fragments that bound to sperm and showed inhibitory activity in a fertilization bioassay. One of these fragments, presumed to be a fragment of the extracellular domain of the receptor, was purified to homogeneity by gel filtration and anion exchange chromatography and shown to be a 70-kD glycosylated protein. Several lines of evidence support the contention that this fragment is derived from the receptor. First, the fragment inhibited fertilization species specifically. Second, species specific binding of the 70-kD glycoprotein to acrosome-reacted sperm was directly demonstrated by using 125I-labeled receptor fragment. Third, the fragment exhibited the same species specificity in binding to isolated bindin particles. Species specificity was abolished by Pronase digestion of the fragment. This observation supports the hypothesis that although binding is mediated by the carbohydrate moieties, species specificity is dependent on the polypeptide backbone. The availability of a structurally defined fragment of the receptor will facilitate further studies of the molecular basis of gamete interaction.
Full Text
The Full Text of this article is available as a PDF (1.3 MB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Bleil J. D., Wassarman P. M. Sperm-egg interactions in the mouse: sequence of events and induction of the acrosome reaction by a zona pellucida glycoprotein. Dev Biol. 1983 Feb;95(2):317–324. doi: 10.1016/0012-1606(83)90032-5. [DOI] [PubMed] [Google Scholar]
- DeAngelis P. L., Glabe C. G. Polysaccharide structural features that are critical for the binding of sulfated fucans to bindin, the adhesive protein from sea urchin sperm. J Biol Chem. 1987 Oct 15;262(29):13946–13952. [PubMed] [Google Scholar]
- Edge A. S., Faltynek C. R., Hof L., Reichert L. E., Jr, Weber P. Deglycosylation of glycoproteins by trifluoromethanesulfonic acid. Anal Biochem. 1981 Nov 15;118(1):131–137. doi: 10.1016/0003-2697(81)90168-8. [DOI] [PubMed] [Google Scholar]
- Gao B., Klein L. E., Britten R. J., Davidson E. H. Sequence of mRNA coding for bindin, a species-specific sea urchin sperm protein required for fertilization. Proc Natl Acad Sci U S A. 1986 Nov;83(22):8634–8638. doi: 10.1073/pnas.83.22.8634. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gibbons I. R., Fronk E. A latent adenosine triphosphatase form of dynein 1 from sea urchin sperm flagella. J Biol Chem. 1979 Jan 10;254(1):187–196. [PubMed] [Google Scholar]
- Glabe C. G., Grabel L. B., Vacquier V. D., Rosen S. D. Carbohydrate specificity of sea urchin sperm bindin: a cell surface lectin mediating sperm-egg adhesion. J Cell Biol. 1982 Jul;94(1):123–128. doi: 10.1083/jcb.94.1.123. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Glabe C. G. Interaction of the sperm adhesive protein, bindin, with phospholipid vesicles. II. Bindin induces the fusion of mixed-phase vesicles that contain phosphatidylcholine and phosphatidylserine in vitro. J Cell Biol. 1985 Mar;100(3):800–806. doi: 10.1083/jcb.100.3.800. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Glabe C. G., Lennarz W. J. Isolation of a high molecular weight glycoconjugate derived from the surface of S purpuratus eggs that is implicated in sperm adhesion. J Supramol Struct Cell Biochem. 1981;15(4):387–394. doi: 10.1002/jsscb.1981.380150408. [DOI] [PubMed] [Google Scholar]
- Glabe C. G., Lennarz W. J. Species-specific sperm adhesion in sea urchins. A quantitative investigation of bindin-mediated egg agglutination. J Cell Biol. 1979 Dec;83(3):595–604. doi: 10.1083/jcb.83.3.595. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Glabe C. G., Vacquier V. D. Egg surface glycoprotein receptor for sea urchin sperm bindin. Proc Natl Acad Sci U S A. 1978 Feb;75(2):881–885. doi: 10.1073/pnas.75.2.881. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Karp D. R., Atkinson J. P., Shreffler D. C. Genetic variation in glycosylation of the fourth component of murine complement. Association with hemolytic activity. J Biol Chem. 1982 Jul 10;257(13):7330–7335. [PubMed] [Google Scholar]
- Kennedy L., DeAngelis P. L., Glabe C. G. Analysis of the membrane-interacting domain of the sea urchin sperm adhesive protein bindin. Biochemistry. 1989 Nov 14;28(23):9153–9158. doi: 10.1021/bi00449a029. [DOI] [PubMed] [Google Scholar]
- Kinsey W. H., Lennarz W. J. Isolation of a glycopeptide fraction from the surface of the sea urchin egg that inhibits sperm-egg binding and fertilization. J Cell Biol. 1981 Nov;91(2 Pt 1):325–331. doi: 10.1083/jcb.91.2.325. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kline D. Calcium-dependent events at fertilization of the frog egg: injection of a calcium buffer blocks ion channel opening, exocytosis, and formation of pronuclei. Dev Biol. 1988 Apr;126(2):346–361. doi: 10.1016/0012-1606(88)90145-5. [DOI] [PubMed] [Google Scholar]
- Kline D., Simoncini L., Mandel G., Maue R. A., Kado R. T., Jaffe L. A. Fertilization events induced by neurotransmitters after injection of mRNA in Xenopus eggs. Science. 1988 Jul 22;241(4864):464–467. doi: 10.1126/science.3134693. [DOI] [PubMed] [Google Scholar]
- LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
- Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
- Moy G. W., Vacquier V. D. Immunoperoxidase localization of bindin during the adhesion of sperm to sea urchin eggs. Curr Top Dev Biol. 1979;13(Pt 1):31–44. doi: 10.1016/s0070-2153(08)60688-2. [DOI] [PubMed] [Google Scholar]
- Rossignol D. P., Earles B. J., Decker G. L., Lennarz W. J. Characterization of the sperm receptor on the surface of eggs of Strongylocentrotus purpuratus. Dev Biol. 1984 Aug;104(2):308–321. doi: 10.1016/0012-1606(84)90086-1. [DOI] [PubMed] [Google Scholar]
- Rossignol D. P., Roschelle A. J., Lennarz W. J. Sperm-egg binding: identification of a species-specific sperm receptor from eggs of Stronglyocentrotus purpuratus. J Supramol Struct Cell Biochem. 1981;15(4):347–358. doi: 10.1002/jsscb.1981.380150405. [DOI] [PubMed] [Google Scholar]
- Ruiz-Bravo N., Earles D., Lennarz W. J. Identification and partial characterization of sperm receptor associated with the newly formed fertilization envelope from sea urchin eggs. Dev Biol. 1986 Sep;117(1):204–208. doi: 10.1016/0012-1606(86)90362-3. [DOI] [PubMed] [Google Scholar]
- Ruiz-Bravo N., Janak D. J., Lennarz W. J. Immunolocalization of the sea urchin sperm receptor in eggs and maturing ovaries. Biol Reprod. 1989 Aug;41(2):323–334. doi: 10.1095/biolreprod41.2.323. [DOI] [PubMed] [Google Scholar]
- Ruiz-Bravo N., Lennarz W. J. Isolation and characterization of proteolytic fragments of the sea urchin sperm receptor that retain species specificity. Dev Biol. 1986 Nov;118(1):202–208. doi: 10.1016/0012-1606(86)90088-6. [DOI] [PubMed] [Google Scholar]
- Schmell E., Earles B. J., Breaux C., Lennarz W. J. Identification of a sperm receptor on the surface of the eggs of the sea urchin Arbacia punctulata. J Cell Biol. 1977 Jan;72(1):35–46. doi: 10.1083/jcb.72.1.35. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Shilling F., Mandel G., Jaffe L. A. Activation by serotonin of starfish eggs expressing the rat serotonin 1c receptor. Cell Regul. 1990 May;1(6):465–469. doi: 10.1091/mbc.1.6.465. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sojar H. T., Bahl O. P. Chemical deglycosylation of glycoproteins. Methods Enzymol. 1987;138:341–350. doi: 10.1016/0076-6879(87)38029-2. [DOI] [PubMed] [Google Scholar]
- Turner P. R., Jaffe L. A., Fein A. Regulation of cortical vesicle exocytosis in sea urchin eggs by inositol 1,4,5-trisphosphate and GTP-binding protein. J Cell Biol. 1986 Jan;102(1):70–76. doi: 10.1083/jcb.102.1.70. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Turner P. R., Jaffe L. A., Primakoff P. A cholera toxin-sensitive G-protein stimulates exocytosis in sea urchin eggs. Dev Biol. 1987 Apr;120(2):577–583. doi: 10.1016/0012-1606(87)90260-0. [DOI] [PubMed] [Google Scholar]
- Vacquier V. D., Moy G. W. Isolation of bindin: the protein responsible for adhesion of sperm to sea urchin eggs. Proc Natl Acad Sci U S A. 1977 Jun;74(6):2456–2460. doi: 10.1073/pnas.74.6.2456. [DOI] [PMC free article] [PubMed] [Google Scholar]