The overall goal of the Protein Identification Core, which will be located within the MS Resource of the Keck Laboratory, will be to identify proteins and their post-translational modifications that are of interest to members of the Neuroproteomics Center and that have been isolated either by individual Center members or by the Protein and Lipid Separation and Profiling Core. In the latter instance, the proteins or peptides of interest may have been determined to be differentially expressed in response to a stimulus or disease based on differential (fluorescence) gel electrophoresis (DIGE) (1), the Beckman-Coulter ProteomeLab PF 2D liquid separation approach (2), or MALDI-MS based biomarker discovery using the algorithm developed by staff in the proposed Bioinformatics and Biostatistics Core (3). In addition to providing existing protein identification technologies to members of the NIDA Neuroproteomies Center, the Protein Identification Core also proposes to extend and improve these technologies.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Center Core Grants (P30)
Project #
5P30DA018343-04
Application #
7440346
Study Section
Special Emphasis Panel (ZDA1)
Project Start
Project End
Budget Start
2007-06-01
Budget End
2008-05-31
Support Year
4
Fiscal Year
2007
Total Cost
$224,992
Indirect Cost
Name
Yale University
Department
Type
DUNS #
043207562
City
New Haven
State
CT
Country
United States
Zip Code
06520
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
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
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

Showing the most recent 10 out of 185 publications