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Originally published as MBC in Press, 10.1091/mbc.E03-11-0843 on February 20, 2004

Vol. 15, Issue 5, 2084-2092, May 2004

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Regulated Proteolysis by Cortical Granule Serine Protease 1 at Fertilization

Sheila A. Haley, and Gary M. Wessel *

Department of Molecular and Cell Biology and Biochemistry; Brown University, Providence, Rhode Island 02916

Submitted November 25, 2003; Revised January 20, 2004; Accepted February 7, 2004
Monitoring Editor: Guido Guidotti

Cortical granules are specialized organelles whose contents interact with the extracellular matrix of the fertilized egg to form the block to polyspermy. In sea urchins, the granule contents form a fertilization envelope (FE), and this construction is critically dependent upon protease activity. An autocatalytic serine protease, cortical granule serine protease 1 (CGSP1), has been identified in the cortical granules of Strongylocentrotus purpuratus eggs, and here we examined the regulation of the protease activity and tested potential target substrates of CGSP1. We found that CGSP1 is stored in its full-length, enzymatically quiescent form in the granule, and is inactive at pH 6.5 or below. We determined the pH of the cortical granule by fluorescent indicators and micro-pH probe measurements and found the granules to be pH 5.5, a condition inhibitory to CGSP1 activity. Exposure of the protease to the pH of seawater (pH 8.0) at exocytosis immediately activates the protease. Activation of eggs at pH 6.5 or lower blocks activation of the protease and the resultant FE phenotypes are indistinguishable from a protease-null phenotype. We find that native cortical granule targets of the protease are {beta}-1,3 glucanase, ovoperoxidase, and the protease itself, but the structural proteins of the granule are not proteolyzed by CGSP1. Whole mount immunolocalization experiments demonstrate that inhibition of CGSP1 activity affects the localization of ovoperoxidase but does not alter targeting of structural proteins to the FE. The mistargeting of ovoperoxidase may lead to spurious peroxidative cross-linking activity and contribute to the lethality observed in protease-null cells. Thus, CGSP1 is proteolytically active only when secreted, due to the low pH of the cortical granules, and it has a small population of targets for cleavage within the cortical granules.


Article published online ahead of print. Mol. Biol. Cell 10.1091/mbc.E03–11–0843. Article and publication date are available at www.molbiolcell.org/cgi/doi/10.1091/mbc.E03–11–0843.

Abbreviations used: ASW, artificial sea water; CGSP1, cortical granule serine protease 1; DTT, dithiothreitol; FE, fertilization envelope; SBTI, soybean trypsin inhibitor.

* Corresponding author. E-mail address: rhet{at}brown.edu.




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