This is the mission of the Biomolecular Mass Spectrometry Facility Core: ? provide exceptional support for environmental health-related research projects using state-of-the-art mass spectral analysis capabilities, ? develop new technologies with the ultimate goal of applying these new technologies to client projects, and ? serve as an educational platform for environmental health science research. The Biomolecular Mass Spectrometry Facility Core (BMSFC) gained its expertise in developing new instruments and ionization technologies over 30 years of measuring pesticides and toxicants in environmental samples. Persistent bioaccumulative toxicants are notoriously difficult to ionize and fragment by mass spectrometry. This challenge has driven much of our development efforts.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Center Core Grants (P30)
Project #
5P30ES000210-44
Application #
8378409
Study Section
Environmental Health Sciences Review Committee (EHS)
Project Start
Project End
Budget Start
2012-04-01
Budget End
2013-03-31
Support Year
44
Fiscal Year
2012
Total Cost
$212,645
Indirect Cost
$67,198
Name
Oregon State University
Department
Type
DUNS #
053599908
City
Corvallis
State
OR
Country
United States
Zip Code
97339
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Vonnegut, Chris L; Shonkwiler, Airlia M; Zakharov, Lev N et al. (2016) Harnessing solid-state packing for selective detection of chloride in a macrocyclic anionophore. Chem Commun (Camb) 52:9506-9
He, Yunteng; Zhang, Jie; Kong, Wei (2016) Electron diffraction of CBr4 in superfluid helium droplets: A step towards single molecule diffraction. J Chem Phys 145:034307
Yang, Liping; Broderick, David; Campbell, Yan et al. (2016) Conformational modulation of the farnesoid X receptor by prenylflavonoids: Insights from hydrogen deuterium exchange mass spectrometry (HDX-MS), fluorescence titration and molecular docking studies. Biochim Biophys Acta 1864:1667-1677
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Li, Feng; Huang, Chun-Hua; Xie, Lin-Na et al. (2016) An Exceptionally Facile Two-Step Structural Isomerization and Detoxication via a Water-Assisted Double Lossen Rearrangement. Sci Rep 6:39207
Hammers, Matthew D; Singh, Loveprit; Montoya, Leticia A et al. (2016) Synthesis of Amino-ADT Provides Access to Hydrolytically Stable Amide-Coupled Hydrogen Sulfide Releasing Drug Targets. Synlett 27:1349-1353
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