IBN-9512113 Roberts, James L. Classical chemical messengers in the central nervous system are simple molecules which upon release are rapidly removed from the site where their actions are exerted. The brain and other bodily tissues also use small protein molecules called peptides as messenger molecules, but the mechanisms in place to terminate their effects are relative unknown. Dr. Roberts and Dr. Glucksman identified a soluble peptide processing and degrading enzyme known as EP 24.15 and established its potential role in modifying peptide actions. However, this enzyme has several unique features, notably that it does not contain a sequence that will allow it to be secreted by classical pathways, and it is located in the nucleus of the cell as well as on the cell surface. These unusual features form the basis for the investigations to be performed by Drs. Roberts and Glucksman. They will examine the intercellular pathway involved in the secretion of EP 24.15 and the mechanisms used by a protein lacking a sequence involved in secretion, to be targeted for secretion. Multiple forms of this enzyme have been identified and the relationship of these forms will be investigated. These exciting studies will reveal novel mechanisms involved in peptide processing and secretion within neuroendocrine cells and have implications for secretory biology, in general.

Agency
National Science Foundation (NSF)
Institute
Division of Integrative Organismal Systems (IOS)
Type
Standard Grant (Standard)
Application #
9512113
Program Officer
Diane M. Witt
Project Start
Project End
Budget Start
1995-09-01
Budget End
1998-08-31
Support Year
Fiscal Year
1995
Total Cost
$153,419
Indirect Cost
Name
Mount Sinai School of Medicine
Department
Type
DUNS #
City
New York
State
NY
Country
United States
Zip Code
10029