CORE 003 ? BIOANALYTICS AND PROTEOMICS SHARED RESOURCE PROJECT SUMMARY/ABSTRACT The mission of the Bioanalytics and Proteomics Shared Resource (BPSR) is to provide cost-effective, state-of- the-art instrumentation and analytical expertise in mass spectrometry to investigators. The BPSR is centrally located on the Vanderbilt campus and is composed of three components that provide the following analytical services: 1) drug and metabolomics analysis, 2) comprehensive proteomics analysis and 3) molecular profiling and tissue imaging. BPSR staff provide consultation on experimental design and sample preparation as well as perform all aspects of mass spectrometry analyses and data analysis. LC-MS/MS, GC-MS and MALDI-TOF instruments are available for small molecule, drug and metabolite analysis. LC-MS/MS instrumentation is available for proteomics analysis, including multiple orbitrap systems. A variety of MALDI-based instruments are provided for molecular profiling and tissue imaging experiments. In addition, inductively coupled plasma mass spectrometry (ICP-MS) capabilities are offered for elemental analysis and tissue imaging. Specific services include identification and quantification of small molecules in biofluids and tissues, identification and quantification of proteins and their modifications by either stable isotope labeling (SILAC and TMT/iTRAQ) or label free methods, crosslinking and hydrogen-deuterium exchange for protein-protein interaction analysis and imaging of small molecules and proteins in tissues using imaging mass spectrometry. The BPSR staff provide education and training in sample preparation, instrument-based experiments and data analysis to VICC investigators and their laboratory personnel. Lastly, the BPSR collaborates with VICC investigators to continue to offer the latest cutting-edge technology and methods in biomolecular mass spectrometry analysis for high- impact cancer discovery.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA068485-25
Application #
10024634
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
1998-09-01
Project End
2025-08-31
Budget Start
2020-09-01
Budget End
2021-08-31
Support Year
25
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Vanderbilt University Medical Center
Department
Type
DUNS #
079917897
City
Nashville
State
TN
Country
United States
Zip Code
37232
Bloodworth, Melissa H; Rusznak, Mark; Pfister, Connor C et al. (2018) Glucagon-like peptide 1 receptor signaling attenuates respiratory syncytial virus-induced type 2 responses and immunopathology. J Allergy Clin Immunol 142:683-687.e12
Saito-Diaz, Kenyi; Benchabane, Hassina; Tiwari, Ajit et al. (2018) APC Inhibits Ligand-Independent Wnt Signaling by the Clathrin Endocytic Pathway. Dev Cell 44:566-581.e8
Cardin, Dana B; Thota, Ramya; Goff, Laura W et al. (2018) A Phase II Study of Ganetespib as Second-line or Third-line Therapy for Metastatic Pancreatic Cancer. Am J Clin Oncol 41:772-776
Hormuth 2nd, David A; Weis, Jared A; Barnes, Stephanie L et al. (2018) Biophysical Modeling of In Vivo Glioma Response After Whole-Brain Radiation Therapy in a Murine Model of Brain Cancer. Int J Radiat Oncol Biol Phys 100:1270-1279
Rojas, Juan D; Lin, Fanglue; Chiang, Yun-Chen et al. (2018) Ultrasound Molecular Imaging of VEGFR-2 in Clear-Cell Renal Cell Carcinoma Tracks Disease Response to Antiangiogenic and Notch-Inhibition Therapy. Theranostics 8:141-155
Dutter, Brendan F; Ender, Anna; Sulikowski, Gary A et al. (2018) Rhodol-based thallium sensors for cellular imaging of potassium channel activity. Org Biomol Chem 16:5575-5579
Vierra, Nicholas C; Dickerson, Matthew T; Jordan, Kelli L et al. (2018) TALK-1 reduces delta-cell endoplasmic reticulum and cytoplasmic calcium levels limiting somatostatin secretion. Mol Metab 9:84-97
Schlegel, Cameron; Weis, Victoria G; Knowles, Byron C et al. (2018) Apical Membrane Alterations in Non-intestinal Organs in Microvillus Inclusion Disease. Dig Dis Sci 63:356-365
Lewis Jr, James S; Shelton, Jeremy; Kuhs, Krystle Lang et al. (2018) p16 Immunohistochemistry in Oropharyngeal Squamous Cell Carcinoma Using the E6H4 Antibody Clone: A Technical Method Study for Optimal Dilution. Head Neck Pathol 12:440-447
Werfel, Thomas A; Wang, Shan; Jackson, Meredith A et al. (2018) Selective mTORC2 Inhibitor Therapeutically Blocks Breast Cancer Cell Growth and Survival. Cancer Res 78:1845-1858

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