Title | Proteome-driven elucidation of adaptive responses to combined vitamin E and C deficiency in zebrafish. |
Publication Type | Journal Article |
Year of Publication | 2014 |
Authors | Motorykin, I, Traber, MG, Tanguay, RL, Maier, CS |
Journal | J Proteome Res |
Volume | 13 |
Issue | 3 |
Pagination | 1647-56 |
Date Published | 2014 Mar 07 |
ISSN | 1535-3907 |
Keywords | Adaptation, Physiological, Animals, Ascorbic Acid, Ascorbic Acid Deficiency, Chromatography, Liquid, Humans, Mass Spectrometry, Metabolic Networks and Pathways, Protein Interaction Mapping, Proteome, Tissue Extracts, Vitamin E, Vitamin E Deficiency, Zebrafish |
Abstract | The purpose of this study was to determine the system-wide consequences of deficiencies in two essential micronutrients, vitamins E and C, on the proteome using zebrafish (Danio rerio) as one of the few vertebrate models that similar to humans cannot synthesize vitamin C. We describe a label-free proteomics workflow to detect changes in protein abundance estimates dependent on vitamin regimes. We used ion-mobility-enhanced data-independent tandem mass spectrometry to determine differential regulation of proteins in response to low dietary levels of vitamin C with or without vitamin E. The detection limit of the method was as low as 20 amol, and the dynamic range was five orders of magnitude for the protein-level estimates. On the basis of the quantitative changes obtained, we built a network of protein interactions that reflect the whole organism's response to vitamin C deficiency. The proteomics-driven study revealed that in vitamin-E-deficient fish, vitamin C deficiency is associated with induction of stress response, astrogliosis, and a shift from glycolysis to glutaminolysis as an alternative mechanism to satisfy cellular energy requirements. |
DOI | 10.1021/pr401108d |
Alternate Journal | J. Proteome Res. |
PubMed ID | 24476500 |
PubMed Central ID | PMC3993953 |
Grant List | S10 RR025628 / RR / NCRR NIH HHS / United States P30ES000210 / ES / NIEHS NIH HHS / United States R01 HD062109 / HD / NICHD NIH HHS / United States R01HD062109 / HD / NICHD NIH HHS / United States S10RR025628 / RR / NCRR NIH HHS / United States P30 ES000210 / ES / NIEHS NIH HHS / United States |