This subproject is one of many research subprojects utilizing theresources provided by a Center grant funded by NIH/NCRR. The subproject andinvestigator (PI) may have received primary funding from another NIH source,and thus could be represented in other CRISP entries. The institution listed isfor the Center, which is not necessarily the institution for the investigator. Description (provided by applicant): The goal of this application is to develop a multidisciplinary Center for the Analysis of Cellular Mechanisms and Systems Biology, to provide new infrastructure to advance understanding of cellular mechanisms, to better understand how to overcome disease, and to build a critical mass of faculty in this area. The Center will be unique in Montana and the five surrounding states, and will include a combination of capabilities for analysis of cellular mechanisms. This project will create a powerful Mass Spectrometry and Proteomics Core infrastructure, oriented toward training researchers. Most cellular mechanisms appear to be controlled by protein post-translational modifications and the MS and Proteomics Core will add: a high resolution Qtof MS for improved 'bottom up' characterization of protein post-translational modifications, an FTMS for 'top-down' characterization of modifications on intact proteins, a Hyperspectral imager for enhanced multicolor proteomic multiplexing to pin-point proteins that change with biological stimulation, and a protein electro-elution system for high efficiency recovery of pin-pointed proteins. Sensitive differential protein detection capabilities developed at MSU and high sensitivity microfluidic nano LC/MS/MS will be included in the Core. New software will integrate data from an existing DNA microarray Facility. A Proteomics Reagent Synthesis Core will prepare new fluorescent reagents for differential analysis of changes in enzyme activity and post-translational modifications that result from biological stimulation. We will build critical mass by first supporting the development of three young faculty and one senior faculty member, who is charting a new course in his research. Outstanding local and national mentors and External Advisory Committee members will guide the development of these faculty and the Center. Second, we will hire four new faculty in areas needed to build critical mass: a Chemical Biologist/Organic Synthesis expert, a Biological Mass Spectroscopist using advanced FTMS tools, a Systems Biologist working on metabolic modeling and metabolomics, and a Cell Biologist using global molecular tools. Outstanding MSU Institutional Support ($1,400,000), the significance and timeliness of the post-genomic analysis of cellular mechanisms, and the orientation toward training in advanced methods will seed new projects-and will result in significant scientific contributions and a sustainable Center.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Exploratory Grants (P20)
Project #
1P20RR024237-01A1
Application #
7721041
Study Section
National Center for Research Resources Initial Review Group (RIRG)
Project Start
2008-09-26
Project End
2009-02-28
Budget Start
2008-09-26
Budget End
2009-02-28
Support Year
1
Fiscal Year
2008
Total Cost
$783,609
Indirect Cost
Name
Montana State University - Bozeman
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
625447982
City
Bozeman
State
MT
Country
United States
Zip Code
59717
Mailhiot, Sarah E; Codd, Sarah L; Brown, Jennifer R et al. (2018) Pulsed gradient stimulated echo (PGStE) NMR shows spatial dependence of fluid diffusion in human stage IV osteoarthritic cartilage. Magn Reson Med 80:1170-1177
McCutchen, Carley N; Zignego, Donald L; June, Ronald K (2017) Metabolic responses induced by compression of chondrocytes in variable-stiffness microenvironments. J Biomech 64:49-58
Folsom, James Patrick; Carlson, Ross P (2015) Physiological, biomass elemental composition and proteomic analyses of Escherichia coli ammonium-limited chemostat growth, and comparison with iron- and glucose-limited chemostat growth. Microbiology 161:1659-70
Folsom, James Patrick; Parker, Albert E; Carlson, Ross P (2014) Physiological and proteomic analysis of Escherichia coli iron-limited chemostat growth. J Bacteriol 196:2748-61
Reeves, B D; Joshi, N; Campanello, G C et al. (2014) Conversion of S-phenylsulfonylcysteine residues to mixed disulfides at pH 4.0: utility in protein thiol blocking and in protein-S-nitrosothiol detection. Org Biomol Chem 12:7942-56
Bernstein, Hans C; Kesaano, Maureen; Moll, Karen et al. (2014) Direct measurement and characterization of active photosynthesis zones inside wastewater remediating and biofuel producing microalgal biofilms. Bioresour Technol 156:206-15
Harvey, Emily; Heys, Jeffrey; Gedeon, Tomáš (2014) Quantifying the effects of the division of labor in metabolic pathways. J Theor Biol 360:222-242
Heinemann, Joshua; Noon, Brigit; Mohigmi, Mohammad J et al. (2014) Real-time digitization of metabolomics patterns from a living system using mass spectrometry. J Am Soc Mass Spectrom 25:1755-62
Jutila, Aaron A; Zignego, Donald L; Hwang, Bradley K et al. (2014) Candidate mediators of chondrocyte mechanotransduction via targeted and untargeted metabolomic measurements. Arch Biochem Biophys 545:116-23
Blosser, Sara J; Merriman, Brittney; Grahl, Nora et al. (2014) Two C4-sterol methyl oxidases (Erg25) catalyse ergosterol intermediate demethylation and impact environmental stress adaptation in Aspergillus fumigatus. Microbiology 160:2492-506

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