This proposal requests funds to acquire a high resolution Fourier transform mass spectrometer and associated liquid chromatography system to support the NIH-funded research of investigators at the University of Cincinnati. This new instrumentation is intended to support on- going NIH-funded research into health-related issues such as antibiotic resistance, atherosclerosis, cancer, diabetes, infectious diseases and obesity. Specifically, the following types of analyses will be enabled by this acquisition: a) Metabolic flu measurements to identify key metabolic pathways in cardiometabolic diseases and various cancers; b) Metabolite identification to support identification of metabolic pathways revealed during metabolic flux measurements; and c) metabolomic characterization of lysophospholipid and cholesterol metabolic pathways. A key group of NIH-supported investigators at the University of Cincinnati will directly benefit from these new capabilities. Moreover, these new capabilities will stimulate these researchers and other biomedical investigators on campus to examine additional experiments that will benefit from this instrument. The NIH-funded researchers participating in this request require dedicated LC-MS/MS or high-resolution ESI/APCI-MS/MS capabilities to accomplish goals associated with their funded projects. The PI, who has been active in the field of mass spectrometry for over 20 years, will be responsible for the managerial oversight of the requested instrumentation. He will report to an external advisory board composed of scientists from within the university. The advisory board will establish scheduling priorities, work with the PI and accounting personnel to establish cost-recovery rates, and will serve as a resource for projecting future use of the requested equipment. The equipment will be housed in the University of Cincinnati Mass Spectrometry Facility. This 3,500 sq. ft. facility is equipped with the ancillary instrumentation required for biomolecule characterization. The instrumentation will be operated and maintained by two Ph.D.-level facility staff scientists, with one of these scientists being designated as the primary operator.

Public Health Relevance

The mass spectrometry system requested will allow NIH-supported researchers access to modern instrumentation to enable research addressing health-related issues such as antibiotic resistance, atherosclerosis, cancer, diabetes, infectious diseases and obesity.

Agency
National Institute of Health (NIH)
Institute
Office of The Director, National Institutes of Health (OD)
Type
Biomedical Research Support Shared Instrumentation Grants (S10)
Project #
1S10OD018485-01
Application #
8734519
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Levy, Abraham
Project Start
2015-04-01
Project End
2016-03-31
Budget Start
2015-04-01
Budget End
2016-03-31
Support Year
1
Fiscal Year
2015
Total Cost
Indirect Cost
Name
University of Cincinnati
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
041064767
City
Cincinnati
State
OH
Country
United States
Zip Code
45221
Sun, Congliang; Jora, Manasses; Solivio, Beulah et al. (2018) The Effects of Ultraviolet Radiation on Nucleoside Modifications in RNA. ACS Chem Biol 13:567-572
Jora, Manasses; Burns, Andrew P; Ross, Robert L et al. (2018) Differentiating Positional Isomers of Nucleoside Modifications by Higher-Energy Collisional Dissociation Mass Spectrometry (HCD MS). J Am Soc Mass Spectrom 29:1745-1756
Jora, Manasses; Lobue, Peter A; Ross, Robert L et al. (2018) Detection of ribonucleoside modifications by liquid chromatography coupled with mass spectrometry. Biochim Biophys Acta Gene Regul Mech :
Addepalli, Balasubrahmanyam; Venus, Sarah; Thakur, Priti et al. (2017) Novel ribonuclease activity of cusativin from Cucumis sativus for mapping nucleoside modifications in RNA. Anal Bioanal Chem 409:5645-5654
Solivio, Morwena J; Nemera, Dessalegn B; Sallans, Larry et al. (2012) Biologically relevant oxidants cause bound proteins to readily oxidatively cross-link at Guanine. Chem Res Toxicol 25:326-36