These studies focus on the structure and function of a previously identified 350kDa glycoprotein on the surface of the sea urchin egg that mediates binding of sperm. Since this binding event is a pre-requisite to fertilization, this information in the long term may be of value in the development of new methods to enhance or prevent fertilization in higher organisms, including humans. Two major questions about the receptor will be addressed. The first question pertains to its mode of localization and biosynthesis. To elucidate the molecular basis for association of the receptor with the cell surface of S. purpuratus eggs, several analytical and biochemical techniques will be applied. These biochemical studies will be complemented by in vivo studies on the biosynthesis of the receptor in starfish oocytes to determine if the full length sea urchin receptor can be synthesized, co- and post- translationally modified, and routed to the cell surface of these oocytes in a functional form. The second question pertains to the mechanism of sperm binding to the receptor. The structure and the function of three structural elements of the receptor known to be involved in sperm binding will be studied. With respect to two of the element, polypeptide domains, deletion and mutational analysis will be performed to define the minimum size and sequence of each required for sperm binding. Also, the significance of the hsp110 homology of the receptor with respect to its function in binding sperm will be studied, particularly with respect to a protein in rat sperm that is believed to be immunologically cross-reactive with hsp70. It will be determined if the third structural element of the receptor, the sulfated O-linked oligosaccharide chains, compete with the two polypeptide domains for binding to sperm, or interact with a different binding site on the sperm. A full understanding of the control of specificity of sperm binding requires a comparison with the primary and complete structure of the receptor from another species of sea urchin. This will be carried out in L. pictus, a sea urchin of another genus that does not cross fertilize with S. purpuratus.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
5R01HD018590-17
Application #
2888891
Study Section
Reproductive Biology Study Section (REB)
Program Officer
Tasca, Richard J
Project Start
1989-08-01
Project End
2002-05-31
Budget Start
1999-06-01
Budget End
2000-05-31
Support Year
17
Fiscal Year
1999
Total Cost
Indirect Cost
Name
State University New York Stony Brook
Department
Biochemistry
Type
Schools of Arts and Sciences
DUNS #
804878247
City
Stony Brook
State
NY
Country
United States
Zip Code
11794
Ohlendieck, Kay (2004) Purification of membrane proteins. Methods Mol Biol 244:301-8
Hirohashi, N; Lennarz, W J (2001) Role of a vitelline layer-associated 350 kDa glycoprotein in controlling species-specific gamete interaction in the sea urchin. Dev Growth Differ 43:247-55
Huggins, L G; Lennarz, W J (2001) Inhibitors of procollagen C-terminal proteinase block gastrulation and spicule elongation in the sea urchin embryo. Dev Growth Differ 43:415-24
Susan, J M; Just, M L; Lennarz, W J (2000) Cloning and characterization of alphaP integrin in embryos of the sea urchin Strongylocentrotus purpuratus. Biochem Biophys Res Commun 272:929-35
Ohta, K; Sato, C; Matsuda, T et al. (2000) Co-localization of receptor and transducer proteins in the glycosphingolipid-enriched, low density, detergent-insoluble membrane fraction of sea urchin sperm. Glycoconj J 17:205-14
Ohta, K; Sato, C; Matsuda, T et al. (1999) Isolation and characterization of low density detergent-insoluble membrane (LD-DIM) fraction from sea urchin sperm. Biochem Biophys Res Commun 258:616-23
Hirohashi, N; Lennarz, W J (1998) The 350-kDa sea urchin egg receptor for sperm is localized in the vitelline layer. Dev Biol 204:305-15
Hirohashi, N; Lennarz, W J (1998) Sperm-egg binding in the sea urchin: a high level of intracellular ATP stabilizes sperm attachment to the egg receptor. Dev Biol 201:270-9
Tian, J; Gong, H; Thomsen, G H et al. (1997) Xenopus laevis sperm-egg adhesion is regulated by modifications in the sperm receptor and the egg vitelline envelope. Dev Biol 187:143-53
Just, M L; Lennarz, W J (1997) Reexamination of the sequence of the sea urchin egg receptor for sperm: implications with respect to its properties. Dev Biol 184:25-30

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