This proposal requests a Finnigan ProteomeX LTQ workstation, an integrated chromatography electrospray ionization linear ion trap mass spectrometer to bring our Basic and Translational Proteomics Center / Shared Research Facility's analytical capability up to state-of-the-art and to increase our capacity to meet the ever increasing volume and intensity of work by our investigators. This request is essential to support our ongoing research programs and to stimulate and enable new collaborative research initiatives on protein identification, posttranslational modification characterization, gene discovery, and functional proteomics. Currently, there is no ESI-LTQ linear ion trap mass spectrometer at the Mount Sinai Medical Center (Hospital and School of Medicine), which provides a fundamental reason for this request. The ProteomeX LTQ workstation is requested in replace of our aged Finnigan LCQ classic mass spectrometer which breaks down so frequently that it seriously affects the on-going research projects. The requested ProteomeX LTQ linear ion trap mass spectrometer will be housed in our Basic and Translational Proteomics Center. The purchase of the ProteomeX LTQ linear ion trap mass spectrometer is fundamental to the continuing expansion and enhancement of the basic research programs and translational proteomics research for human disease on the Mount Sinai campus. As described in this application, over 22 NIH-funded investigators from 10 different departments and two NIH-funded investigators from neighboring institutes have specific needs for this mass spectrometer, which will be a shared research resource. Indeed, due to the lack of an highly sensitive and high throughput proteomics instrument on campus, some of these research projects are seriously delayed or compromised. Thus, the purchase of the ProteomeX LTQ system will have a major impact on the research capabilities at our institution. ? ?

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biomedical Research Support Shared Instrumentation Grants (S10)
Project #
1S10RR022415-01
Application #
7044524
Study Section
Special Emphasis Panel (ZRG1-BCMB-D (30))
Program Officer
Tingle, Marjorie
Project Start
2006-03-15
Project End
2008-03-14
Budget Start
2006-03-15
Budget End
2008-03-14
Support Year
1
Fiscal Year
2006
Total Cost
$424,073
Indirect Cost
Name
Mount Sinai School of Medicine
Department
Genetics
Type
Schools of Medicine
DUNS #
078861598
City
New York
State
NY
Country
United States
Zip Code
10029
Choi, Soon Gang; Wang, Qian; Jia, Jingjing et al. (2016) Characterization of Gonadotrope Secretoproteome Identifies Neurosecretory Protein VGF-derived Peptide Suppression of Follicle-stimulating Hormone Gene Expression. J Biol Chem 291:21322-21334
Lim, Junghyun; Lachenmayer, M Lenard; Wu, Shuai et al. (2015) Proteotoxic stress induces phosphorylation of p62/SQSTM1 by ULK1 to regulate selective autophagic clearance of protein aggregates. PLoS Genet 11:e1004987
Wang, Yuan; Kou, Yan; Wang, Xiaodong et al. (2014) Multifactorial comparative proteomic study of cytochrome P450 2E1 function in chronic alcohol administration. PLoS One 9:e92504
Zhang, Xulun; Hoey, Robert; Koide, Akiko et al. (2014) A synthetic antibody fragment targeting nicastrin affects assembly and trafficking of ?-secretase. J Biol Chem 289:34851-61
Mendoza, Jhoana; Sekiya, Michiko; Taniguchi, Taizo et al. (2013) Global analysis of phosphorylation of tau by the checkpoint kinases Chk1 and Chk2 in vitro. J Proteome Res 12:2654-65
Steele, J W; Lachenmayer, M L; Ju, S et al. (2013) Latrepirdine improves cognition and arrests progression of neuropathology in an Alzheimer's mouse model. Mol Psychiatry 18:889-97
Steele, J W; Ju, S; Lachenmayer, M L et al. (2013) Latrepirdine stimulates autophagy and reduces accumulation of ?-synuclein in cells and in mouse brain. Mol Psychiatry 18:882-8
Zhang, Xulun; Hoey, Robert J; Lin, Guoqing et al. (2012) Identification of a tetratricopeptide repeat-like domain in the nicastrin subunit of ýý-secretase using synthetic antibodies. Proc Natl Acad Sci U S A 109:8534-9
Keilani, Serene; Chandwani, Samira; Dolios, Georgia et al. (2012) Egr-1 induces DARPP-32 expression in striatal medium spiny neurons via a conserved intragenic element. J Neurosci 32:6808-18
Abul-Husn, Noura S; Bushlin, Ittai; Morón, José A et al. (2009) Systems approach to explore components and interactions in the presynapse. Proteomics 9:3303-15

Showing the most recent 10 out of 12 publications