The Iron and Heme Core of the Center for Iron and Heme Disorders (CIHD) will provide analysis of metals, porphyrins, porphyrin precursors and heme. The Core will measure enzymatic activity of the eight enzymes of the heme biosynthesis pathway. This Core is unique in the services offered. Analysis and absolute quantitation of many of these compounds in cells, tissue, whole blood, urine and feces will become available to laboratories nationally. The Core will also provide a series of reagents, including plasmids for expression of proteins in heme synthesis, antibodies reactive to these proteins, and unique strains of bacteria that can be used to purify porphyrin pathway intermediates for use in other experimental systems. Core staff will host training sessions to assist PIs, post-doctoral fellows and graduate students in performing the services above, including sessions aimed at data analysis. CIHD investigators will be provided priority access to these services through dedicated Core staff. It is the goal of the Iron and Heme Core to become a national resource for the measurement of these enzymes/compounds in a diverse range of experimental systems from bacteria to human.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Specialized Center--Cooperative Agreements (U54)
Project #
5U54DK110858-02
Application #
9325529
Study Section
Special Emphasis Panel (ZDK1)
Project Start
Project End
Budget Start
2017-08-01
Budget End
2018-07-31
Support Year
2
Fiscal Year
2017
Total Cost
Indirect Cost
Name
University of Utah
Department
Type
DUNS #
009095365
City
Salt Lake City
State
UT
Country
United States
Zip Code
84112
Yuan, Xiaojing; Hamza, Iqbal (2018) Cys Links Heme: Stereo-orientation of Heme Transfer in Cytochrome c Biogenesis. J Mol Biol 430:1081-1083
García-Guerrero, Aldo E; Camacho-Villasana, Yolanda; Zamudio-Ochoa, Angélica et al. (2018) Cbp3 and Cbp6 are dispensable for synthesis regulation of cytochrome b in yeast mitochondria. J Biol Chem 293:5585-5599
Schumann, Canan; Chan, Stephanie; Millar, Jess A et al. (2018) Intraperitoneal nanotherapy for metastatic ovarian cancer based on siRNA-mediated suppression of DJ-1 protein combined with a low dose of cisplatin. Nanomedicine 14:1395-1405
Akam, E A; Utterback, R D; Marcero, J R et al. (2018) Disulfide-masked iron prochelators: Effects on cell death, proliferation, and hemoglobin production. J Inorg Biochem 180:186-193
Ryu, Moon-Suhn; Duck, Kari A; Philpott, Caroline C (2018) Ferritin iron regulators, PCBP1 and NCOA4, respond to cellular iron status in developing red cells. Blood Cells Mol Dis 69:75-81
Chen, Andy Jing; Yuan, Xiaojing; Li, Junjie et al. (2018) Label-Free Imaging of Heme Dynamics in Living Organisms by Transient Absorption Microscopy. Anal Chem 90:3395-3401
Lambert, Christopher J; Freshner, Briana C; Chung, Arlen et al. (2018) An automated system for rapid cellular extraction from live zebrafish embryos and larvae: Development and application to genotyping. PLoS One 13:e0193180
Vázquez-Arreguín, Karina; Maddox, Jessica; Kang, Jinsuk et al. (2018) BRCA1 through Its E3 Ligase Activity Regulates the Transcription Factor Oct1 and Carbohydrate Metabolism. Mol Cancer Res 16:439-452
Tsushima, Kensuke; Bugger, Heiko; Wende, Adam R et al. (2018) Mitochondrial Reactive Oxygen Species in Lipotoxic Hearts Induce Post-Translational Modifications of AKAP121, DRP1, and OPA1 That Promote Mitochondrial Fission. Circ Res 122:58-73
Burch, Joseph S; Marcero, Jason R; Maschek, John Alan et al. (2018) Glutamine via ?-ketoglutarate dehydrogenase provides succinyl-CoA for heme synthesis during erythropoiesis. Blood 132:987-998

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