The focus of this project resides on the role of small antioxidant molecules on the prevention and/or repair of nitrated proteins in mitochondria. Protein nitration occurs in biological systems exposed to nitric oxide. The addition of a nitro group to a tyrosine residue, yielding 3-nitrotyrosine, has been claimed to be a posttranslational modification, part of signal transduction pathways, or a result of """"""""normal"""""""" oxidative stress. In this study, we will characterize the mechanism underlying the nitration of proteins in nitric oxide-producing mitochondria, given the important role that these organelles have in the maintenance of cellular ATP, beta-oxidation, heme synthesis, and other functions. Our studies will be aimed at understanding the kinetic and structural changes caused by nitration, and how naturally occurring antioxidants -- present in fruits and vegetables may prevent/reverse this effect. The antioxidant effect of flavonoids, coumarins, and catechins will be studied in terms of hydroxyl substitution, conjugation of rings, and o-methylation of hydroxyl groups to elucidate an association between structure and function. To this end, the specific aims of this proposal are the following: 1. Investigate the molecular mechanisms of mitochondrial protein nitration 2. Elucidate the biological relevance of protein nitration in mitochondria 3. Structure-activity association of naturally occurring flavonoids in the abrogation of protein nitration, and 4. Bioavailability of flavonoids containing diets in nitrative stress.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Research Project (R01)
Project #
7R01ES012691-02
Application #
7010952
Study Section
Xenobiotic and Nutrient Disposition and Action Study Section (XNDA)
Program Officer
Maull, Elizabeth A
Project Start
2004-09-23
Project End
2007-08-31
Budget Start
2004-09-25
Budget End
2007-08-31
Support Year
2
Fiscal Year
2004
Total Cost
$147,996
Indirect Cost
Name
University of California Davis
Department
Biochemistry
Type
Schools of Veterinary Medicine
DUNS #
047120084
City
Davis
State
CA
Country
United States
Zip Code
95618
Napoli, Eleonora; Liu, Siming; Marsilio, Ilaria et al. (2017) Lipid-based DNA/siRNA transfection agents disrupt neuronal bioenergetics and mitophagy. Biochem J 474:3887-3902
Napoli, Eleonora; Song, Gyu; Liu, Siming et al. (2017) Zdhhc13-dependent Drp1 S-palmitoylation impacts brain bioenergetics, anxiety, coordination and motor skills. Sci Rep 7:12796
Giulivi, Cecilia; Napoli, Eleonora; Tassone, Flora et al. (2016) Plasma Biomarkers for Monitoring Brain Pathophysiology in FMR1 Premutation Carriers. Front Mol Neurosci 9:71
Napoli, Eleonora; Song, Gyu; Wong, Sarah et al. (2016) Altered Bioenergetics in Primary Dermal Fibroblasts from Adult Carriers of the FMR1 Premutation Before the Onset of the Neurodegenerative Disease Fragile X-Associated Tremor/Ataxia Syndrome. Cerebellum 15:552-64
Napoli, Eleonora; Song, Gyu; Schneider, Andrea et al. (2016) Warburg effect linked to cognitive-executive deficits in FMR1 premutation. FASEB J 30:3334-3351
Song, Gyu; Napoli, Eleonora; Wong, Sarah et al. (2016) Altered redox mitochondrial biology in the neurodegenerative disorder fragile X-tremor/ataxia syndrome: use of antioxidants in precision medicine. Mol Med 22:548-559
Giulivi, Cecilia; Napoli, Eleonora; Tassone, Flora et al. (2016) Plasma metabolic profile delineates roles for neurodegeneration, pro-inflammatory damage and mitochondrial dysfunction in the FMR1 premutation. Biochem J 473:3871-3888
Wong, Sarah; Giulivi, Cecilia (2016) Autism, Mitochondria and Polybrominated Diphenyl Ether Exposure. CNS Neurol Disord Drug Targets 15:614-23
Fujisawa, Yasuko; Napoli, Eleonora; Wong, Sarah et al. (2015) Impact of a novel homozygous mutation in nicotinamide nucleotide transhydrogenase on mitochondrial DNA integrity in a case of familial glucocorticoid deficiency. BBA Clin 3:70-78
Vernau, Karen; Napoli, Eleonora; Wong, Sarah et al. (2015) Thiamine Deficiency-Mediated Brain Mitochondrial Pathology in Alaskan Huskies with Mutation in SLC19A3.1. Brain Pathol 25:441-53

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