The mission of the MS Core is to provide cost effective, state-of-the-art instrumentation and analytical expertise to investigators in the Center for Molecular Toxicology for identification of protein and DNA adducts, biophysical and structural analysis of proteins, and for qualitative and quantitative assays of metabolites in tissues and cells. The MS Core is used extensively by eleven of the Center in Molecular Toxicology investigators. Laboratory personnel assist users in developing analytical methods, assist in experimental design, develop standard operating procedures, maintain quality control records on instrument performance and maintenance history, perform routine assays for investigators and train students and fellows in the theoretical and practical aspects of MS. The Core is run as an open-access facility in which users are expected to prepare their own samples and to operate the instruments if they so desire. Administrative staff monitors the use of the instrument facilities by investigators and prepares reports on utilization. The Core has five triple quadrupole liquid chromatography (LC)/MS instruments, one LC/MS ion trap instrument, an electrospray ionization time-of-flight MS (ESI-TOF), two GC/MS systems, and a matrix-assisted laser desorption ionization (MALDI) mass spectrometer. The MS Core is part of the Vanderbilt University Mass Spectrometry Research Center, a comprehensive research unit located in the Medical School. This facility consists of a Core MS service laboratory and the Proteomics Research Core. In addition to providing routine analytical and MS services via the various Core facilities, investigators can form collaborations to solve analytical and structural problems that require non-routine, cutting edge technology. As newer techniques become better understood, they will be made available to the user community through the Core service laboratory. Thus, the Core satisfies the routine analytical needs of investigators and also makes available new analytical capabilities for research problems demanding more innovative solutions that are beyond the scope of a service laboratory. In addition, a training program on various aspects of MS is offered so users can learn to operate the instruments, design experiments, and interpret analytical results more effectively. Both the Core and Research laboratories were extensively renovated in 1998 and new instrumentation was purchased to provide a state-of-the-art facility. Support for the facility comes from service cores affiliated with eight NIH-funded Program Projects and Research Centers, service fees charged to unaffiliated investigators and direct institutional support form Vanderbilt University.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Center Core Grants (P30)
Project #
5P30ES000267-39
Application #
7063139
Study Section
Environmental Health Sciences Review Committee (EHS)
Project Start
Project End
Budget Start
2005-04-01
Budget End
2006-03-31
Support Year
39
Fiscal Year
2005
Total Cost
$189,667
Indirect Cost
Name
Vanderbilt University Medical Center
Department
Type
DUNS #
004413456
City
Nashville
State
TN
Country
United States
Zip Code
37212
Wages, Phillip A; Kim, Hye-Young H; Korade, Zeljka et al. (2018) Identification and characterization of prescription drugs that change levels of 7-dehydrocholesterol and desmosterol. J Lipid Res 59:1916-1926
Sha, Yan; Minko, Irina G; Malik, Chanchal K et al. (2017) Error-prone replication bypass of the imidazole ring-opened formamidopyrimidine deoxyguanosine adduct. Environ Mol Mutagen 58:182-189
Sugitani, Norie; Voehler, Markus W; Roh, Michelle S et al. (2017) Analysis of DNA binding by human factor xeroderma pigmentosum complementation group A (XPA) provides insight into its interactions with nucleotide excision repair substrates. J Biol Chem 292:16847-16857
Minko, Irina G; Rizzo, Carmelo J; Lloyd, R Stephen (2017) Mutagenic potential of nitrogen mustard-induced formamidopyrimidine DNA adduct: Contribution of the non-canonical ?-anomer. J Biol Chem 292:18790-18799
Rivara, Matthew B; Yeung, Catherine K; Robinson-Cohen, Cassianne et al. (2017) Effect of Coenzyme Q10 on Biomarkers of Oxidative Stress and Cardiac Function in Hemodialysis Patients: The CoQ10 Biomarker Trial. Am J Kidney Dis 69:389-399
Yan, H P; Roberts, L J; Davies, S S et al. (2017) Isolevuglandins as a gauge of lipid peroxidation in human tumors. Free Radic Biol Med 106:62-68
Neely, M Diana; Davison, Carrie Ann; Aschner, Michael et al. (2017) From the Cover: Manganese and Rotenone-Induced Oxidative Stress Signatures Differ in iPSC-Derived Human Dopamine Neurons. Toxicol Sci 159:366-379
Caito, Samuel W; Aschner, Michael (2016) NAD+ Supplementation Attenuates Methylmercury Dopaminergic and Mitochondrial Toxicity in Caenorhabditis Elegans. Toxicol Sci 151:139-49
Wakeman, Catherine A; Moore, Jessica L; Noto, Michael J et al. (2016) The innate immune protein calprotectin promotes Pseudomonas aeruginosa and Staphylococcus aureus interaction. Nat Commun 7:11951
Sloan, Chantel D; Gebretsadik, Tebeb; Rosas-Salazar, Christian et al. (2016) Seasonal Timing of Infant Bronchiolitis, Apnea and Sudden Unexplained Infant Death. PLoS One 11:e0158521

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