We propose to establish a NIDA Neuroproteomics Research Center at the Yale University School of Medicine. More than 20 faculty members with an established history of studies of the molecular actions of psychostimulants and psychotropic drugs, as well as of other basic aspects of neurobiology, will work together with the W.M. Keck Foundation Biotechnology Resource Laboratory to create the Neuroproteomics Center. The main goal of the Center will be to apply high-throughput, state-of-the-art proteomic technologies to analyze adaptive changes in neuronal protein expression and regulation that occur in response to drugs of abuse. In addition, the Center will provide training in proteomics technologies, and will improve existing and develop new proteomies technologies that can be applied to biological questions related to the actions of drugs of abuse. The Center will include five cores: Protein Separation and Profiling, Protein Identification, Protein Microarray, Bioinformatics and Biostatistics, and Administration. A """"""""lipidomics"""""""" component, included in the Protein Separation Core, will also allow the analysis of cellular lipids. The behavioral adaptations that accompany drug addiction are believed to result from both short and longterm adaptive changes in brain reward centers. To date, molecular studies of drugs of abuse have elucidated some of the transcriptional changes that occur in the addicted brain. However, little is known about the effects of drugs of abuse on the neuronal proteome. The Center will, through its highly interdisciplinary and collaborative organization, bring together Yale faculty with complementary expertise to gain a far deeper insight into how drugs of abuse alter expression and post-translational modification of proteins on a global scale. Methods that will be used will include MALDI-MS based biomarker analysis, two-dimensional chromatography, differential (fluorescence) gel electrophoresis (DIGE), isotope-coded affinity tag (ICAT), and antibody microarrays. Methods also will be developed for studying the brain phosphoproteome and these will be applied to studies of the actions of drugs of abuse. Specific goals of the research supported by the Center include analysis of the actions of opiates; the psychostimulants, cocaine and amphetamine; and nicotine on protein expression. Other studies will focus on the proteomic changes that occur both pre- and post-synaptically following the actions of drugs of abuse.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Center Core Grants (P30)
Project #
5P30DA018343-05
Application #
7440348
Study Section
Special Emphasis Panel (ZDA1-RXL-E (21))
Program Officer
Pollock, Jonathan D
Project Start
2004-08-23
Project End
2009-09-29
Budget Start
2008-06-01
Budget End
2009-09-29
Support Year
5
Fiscal Year
2008
Total Cost
$1,514,432
Indirect Cost
Name
Yale University
Department
Biochemistry
Type
Schools of Medicine
DUNS #
043207562
City
New Haven
State
CT
Country
United States
Zip Code
06520
Benedetti, Lorena; Barentine, Andrew E S; Messa, Mirko et al. (2018) Light-activated protein interaction with high spatial subcellular confinement. Proc Natl Acad Sci U S A 115:E2238-E2245
Rao, Vishwanatha K; Zavala, Gerardo; Deb Roy, Abhijit et al. (2018) A pH-sensitive luminal His-cluster promotes interaction of PAM with V-ATPase along the secretory and endocytic pathways of peptidergic cells. J Cell Physiol :
Bian, Xin; Saheki, Yasunori; De Camilli, Pietro (2018) Ca2+ releases E-Syt1 autoinhibition to couple ER-plasma membrane tethering with lipid transport. EMBO J 37:219-234
Wilson, Rashaun S; Nairn, Angus C (2018) Making brain proteomics true to type. Nat Biotechnol 36:149-150
Li, Daniel; Musante, Veronica; Zhou, Wenliang et al. (2018) Striatin-1 is a B subunit of protein phosphatase PP2A that regulates dendritic arborization and spine development in striatal neurons. J Biol Chem 293:11179-11194
Levy, Aaron D; Xiao, Xiao; Shaw, Juliana E et al. (2018) Noonan Syndrome-Associated SHP2 Dephosphorylates GluN2B to Regulate NMDA Receptor Function. Cell Rep 24:1523-1535
Mervosh, Nicholas L; Wilson, Rashaun; Rauniyar, Navin et al. (2018) Granulocyte-Colony-Stimulating Factor Alters the Proteomic Landscape of the Ventral Tegmental Area. Proteomes 6:
Kumar, Nikit; Leonzino, Marianna; Hancock-Cerutti, William et al. (2018) VPS13A and VPS13C are lipid transport proteins differentially localized at ER contact sites. J Cell Biol 217:3625-3639
Milovanovic, Dragomir; Wu, Yumei; Bian, Xin et al. (2018) A liquid phase of synapsin and lipid vesicles. Science 361:604-607
Carlyle, Becky C; Kitchen, Robert R; Kanyo, Jean E et al. (2017) A multiregional proteomic survey of the postnatal human brain. Nat Neurosci 20:1787-1795

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