This core will produce proteins that will be used for several different purposes: structure determination using both X-ray crystallography and NMR; metal binding analyses; analysis of posttranslational modification in response to metals; metal transport measurements using liposome reconstitution and for injection into animals to generate antibodies. The Protein Purification Core will purify proteins from large-scale cultures of bacteria; bacculovirus infected insect cells and yeast. While most members of the CEMH use protein expression in their laboratories, there are several reasons to centralize protein expression. First, the Core will centralize both expertise and reagents. The Core will contain a catalogue of bacterial expressions systems, permitting the production and purification of epitope tagged proteins (HIS, GST, Maltose, TAP) in large amounts. Second, the scale of the Core will be designed to accommodate the need to produce different levels of proteins from the relatively small amounts required for antibody production (mg) to metal binding assay (10 mg) to X-Ray crystallography (100's mg).

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
5P30DK072437-02
Application #
7311642
Study Section
Special Emphasis Panel (ZDK1)
Project Start
Project End
Budget Start
2006-09-01
Budget End
2007-08-31
Support Year
2
Fiscal Year
2006
Total Cost
$166,437
Indirect Cost
Name
University of Utah
Department
Type
DUNS #
009095365
City
Salt Lake City
State
UT
Country
United States
Zip Code
84112
Hibbs Jr, John B; Vavrin, Zdenek; Cox, James E (2016) Complex coordinated extracellular metabolism: Acid phosphatases activate diluted human leukocyte proteins to generate energy flow as NADPH from purine nucleotide ribose. Redox Biol 8:271-84
Philip, Mary; Funkhouser, Scott A; Chiu, Edison Y et al. (2015) Heme exporter FLVCR is required for T cell development and peripheral survival. J Immunol 194:1677-85
Shah, Dhvanit I; Takahashi-Makise, Naoko; Cooney, Jeffrey D et al. (2012) Mitochondrial Atpif1 regulates haem synthesis in developing erythroblasts. Nature 491:608-12
Chen, Caiyong; Paw, Barry H (2012) Cellular and mitochondrial iron homeostasis in vertebrates. Biochim Biophys Acta 1823:1459-67
Bricker, Daniel K; Taylor, Eric B; Schell, John C et al. (2012) A mitochondrial pyruvate carrier required for pyruvate uptake in yeast, Drosophila, and humans. Science 337:96-100
Lorenzo 5th, Felipe R; Phillips, John D; Nussenzveig, Roberto et al. (2011) Molecular basis of two novel mutations found in type I methemoglobinemia. Blood Cells Mol Dis 46:277-81
Wang, Yongming; Langer, Nathaniel B; Shaw, George C et al. (2011) Abnormal mitoferrin-1 expression in patients with erythropoietic protoporphyria. Exp Hematol 39:784-94
Gleason, Julie E; Corrigan, David J; Cox, James E et al. (2011) Analysis of hypoxia and hypoxia-like states through metabolite profiling. PLoS One 6:e24741
Amigo, Julio D; Yu, Ming; Troadec, Marie-Berengere et al. (2011) Identification of distal cis-regulatory elements at mouse mitoferrin loci using zebrafish transgenesis. Mol Cell Biol 31:1344-56
Li, Liangtao; Murdock, Grace; Bagley, Dustin et al. (2010) Genetic dissection of a mitochondria-vacuole signaling pathway in yeast reveals a link between chronic oxidative stress and vacuolar iron transport. J Biol Chem 285:10232-42

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