Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Echinobase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Echinobase
ECB-ART-39160
Biochem Biophys Res Commun 2004 Aug 13;3211:88-93. doi: 10.1016/j.bbrc.2004.06.109.
Show Gene links Show Anatomy links

Ion channel activity of membrane vesicles released from sea urchin sperm during the acrosome reaction.

Schulz JR , De la Vega-Beltrán JL , Beltrán C , Vacquier VD , Darszon A .


???displayArticle.abstract???
The sperm acrosome reaction (AR) involves ion channel activation. In sea urchin sperm, the AR requires Ca2+ and Na+ influx and K+ and H+ efflux. During the AR, the plasma membrane fuses with the acrosomal vesicle membrane forming hybrid membrane vesicles that are released from sperm into the medium. This paper reports the isolation and preliminary characterization of these acrosome reaction vesicles (ARVs), using synaptosome-associated protein of 25 kDa (SNAP-25) as a marker. Isolated ARVs have a unique protein composition. The exocytosis regulatory proteins vesicle-associated membrane protein and SNAP-25 are inside ARVs, as judged by protease protection experiments, and membrane associated based on Triton X-114 partitioning. ARVs fused with planar bilayers display three main types of single channel activity. The most frequently recorded channel is cationic, weakly voltage dependent and has a low open probability that increases with negative potentials. This channel is activated by cAMP, blocked by Ba2+, and has a PK+/PNa+ selectivity of 4.5. ARVs represent a novel membrane preparation suitable to deepen our understanding of ion channel activity in the AR and during fertilization.

???displayArticle.pubmedLink??? 15358219
???displayArticle.link??? Biochem Biophys Res Commun
???displayArticle.grants??? [+]

Genes referenced: LOC100887844 LOC752081 LOC756768 mpp5 stk36
???displayArticle.antibodies??? snap25 Ab1