The specific aims of the present research proposal are directed at identifying and characterizing taste cell-expressed proteinsthat enhance taste receptor function. In vivo, these proteins may play a role in optimizingtaste cell function, or they could play a role in adaptationto external taste stimuli by regulating the number offunctional receptors at the taste cell surface. Taste tissue will be analyzed by PCR techniques to screen for thepresence of members of the RTF and Reep families, which may function to enhance taste receptor activity.Each RTF and Reep protein found in taste will be tested for its enhancingpropertieson tastant receptors usingexpressed taste receptors in heterologous cells. Any potential interactions of RTFs or Reeps with tastereceptors will be confirmed by immunoprecipitation and confocal microscopy.Finally, the mechanismofaction of these enhancing proteinswill be investigatedusing structural and functional studies.

Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32DC008240-03
Application #
7365174
Study Section
Communication Disorders Review Committee (CDRC)
Program Officer
Cyr, Janet
Project Start
2006-03-31
Project End
2008-06-13
Budget Start
2008-03-31
Budget End
2008-06-13
Support Year
3
Fiscal Year
2008
Total Cost
$12,306
Indirect Cost
Name
Icahn School of Medicine at Mount Sinai
Department
Neurosciences
Type
Schools of Medicine
DUNS #
078861598
City
New York
State
NY
Country
United States
Zip Code
10029
Ilegems, Erwin; Iwatsuki, Ken; Kokrashvili, Zaza et al. (2010) REEP2 enhances sweet receptor function by recruitment to lipid rafts. J Neurosci 30:13774-83