Authors

Ye Zhang

Type

Text

Type

Thesis

Advisor

Laughlin, Scott T | Sampson, Nicole S | Grubbs, Robert B

Date

2017-12-01

Keywords

Chemistry | Acrosomal exocytosis | Calcium | Sperm

Department

Department of Chemistry

Language

en_US

Source

This work is sponsored by the Stony Brook University Graduate School in compliance with the requirements for completion of degree.

Identifier

http://hdl.handle.net/11401/78235

Publisher

The Graduate School, Stony Brook University: Stony Brook, NY.

Format

application/pdf

Abstract

Sperm acrosomal exocytosis plays an important role in mammalian fertilization. This exocytosis process can be triggered by a subset of terminal carbohydrate residues on the zona pellucida around the mouse egg. Although acrosomal exocytosis (AE) has been successfully induced in vitro using purified mouse zona pellucida protein, the mechanism of AE is unclear. Previous studies in the Sampson laboratory used a series of glycopolymers that mimic the sugars displayed by the zona pellucida and applied these polymers in an in vitro acrosome assay. The Ca2+-selective ion channel subunits (CatSper) were thought to be the essential ion channel for regulating Ca2+ influx, and intracellular Ca2+ is a crucial factor for successful AE. To understand the Ca2+ dependence of the glycopolymer-induced in vitro AE, we applied a triple stain strategy and flow cytometry technique to test the Ca2+ dependence in the presence and absence of EGTA (ethylene glycol tetraacetic acid). Three glycopolymers [poly-(mannose)100, poly-(fucose)100 and poly-(glcNAc)100] show clear Ca2+ dependence. | 94 pages

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