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Purification and identification of secernin, a novel cytosolic protein that regulates exocytosis in mast cells

Way, G.; Morrice, N.; Smythe, C.; O'Sullivan, A.J.

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Authors

G. Way

N. Morrice

C. Smythe

A.J. O'Sullivan



Abstract

After permeabilization with the pore-forming toxin streptolysin-O mast cells can be triggered to secrete by addition of both calcium and a GTP analogue. If stimulation is delayed after permeabilization, there is a progressive decrease in the extent of secretion upon stimulation, eventually leading to a complete loss of the secretory response. This loss of secretory response can be retarded by the addition of cytosol from other secretory tissues, demonstrating that the response is dependent on a number of cytosolic proteins. We have used this as the basis of a bioassay to purify Secernin 1, a novel 50-kDa cytosolic protein that appears to be involved in the regulation of exocytosis from peritoneal mast cells. Secernin 1 increases both the extent of secretion and increases the sensitivity of mast cells to stimulation with calcium.

Citation

Way, G., Morrice, N., Smythe, C., & O'Sullivan, A. (2002). Purification and identification of secernin, a novel cytosolic protein that regulates exocytosis in mast cells. Molecular Biology of the Cell, 13(9), 3344-3354. https://doi.org/10.1091/mbc.e01-10-0094

Journal Article Type Article
Publication Date Sep 1, 2002
Deposit Date Oct 1, 2008
Publicly Available Date Oct 1, 2008
Journal Molecular biology of the cell
Publisher American Society for Cell Biology
Peer Reviewed Peer Reviewed
Volume 13
Issue 9
Pages 3344-3354
DOI https://doi.org/10.1091/mbc.e01-10-0094
Keywords Permeabilized cells, Hematopoietic-cells, Chromaffin cells, Membrane-fusion, Streptolysin-O, Kinase-C, Secretion, RAC.
Publisher URL http://www.molbiolcell.org/cgi/content/full/13/9/3344

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Copyright Statement
© 2002 by The American Society for Cell Biology




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