Phase II drug metabolizing enzymes sulfotransferases (SULTs) catalyzed sulfation is important in the regulation of different hormones and the detoxification of drugs and other xenobiotics. Sulfation also leads to bioactivation of procarcinogens leading to toxic effect. The long-term goal of this research project is to understand human SULT biological functions and to investigate their relevance to human health under physiological and pathological conditions.
Specific aims i n this proposal are as follows: 1. To investigate mechanisms of catalysis, substrate inhibition, and product inhibition/activation of human SULTs. The proposed bypass ordered mechanism and related alternative mechanisms will be investigated using kinetic analysis, isotope exchange, sulfated active site amino acid residue identification, and site-directed mutagenesis. The information will have important implications for the prediction of biotransformation pathways. 2. To investigate the effect of sulfated drugs on human SULT catalytic activities. The inhibition and activation effect of clinically important drug sulfates on catalytic activities of human SULTs will be investigated. E. coli expressed and purified human SULTs; human intestinal cytosols; and human Hep G2 and Caco-2 cells will be used for these investigations. The effect of clinical drugs on human SULT activities may interfere SULT normal biological functions in hormone regulation and xenobiotic detoxification. 3. To define oxidative regulation mechanisms of human SULT1E1. Oxidative regulation of human SULT1E1 in Hep G2 and Caco-2 cells and redox thiol regulation mechanisms of purified human SULT1E1 will be investigated using enzyme assay, Western blot, RT-PCR, amino acid modification, site-directed mutagenesis, kinetic analysis, crystal structure analysis, and computer modeling methods. Knowledge on oxidative regulation of certain human SULT is important in understanding the ability of SULT functioning under physiological and pathological conditions. This proposal studies human SULTs. These studies will be significant in understanding SULT biological functions including hormone regulation, drug metabolism, xenobiotic detoxification and procarcinogen bioactivation. The knowledge will be important in understanding drug side effect, drug-drug interaction, drug development, and the potential roles SULTs play in cancer prevention and causation. ? ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
1R01GM078606-01
Application #
7135375
Study Section
Xenobiotic and Nutrient Disposition and Action Study Section (XNDA)
Program Officer
Okita, Richard T
Project Start
2006-09-22
Project End
2010-08-31
Budget Start
2006-09-22
Budget End
2007-08-31
Support Year
1
Fiscal Year
2006
Total Cost
$253,686
Indirect Cost
Name
Oklahoma State University Stillwater
Department
Physiology
Type
Schools of Veterinary Medicine
DUNS #
049987720
City
Stillwater
State
OK
Country
United States
Zip Code
74078
Huang, Chaoqun; Zhou, Tianyan; Chen, Yue et al. (2014) Estrogen-related receptor ERR? regulation of human hydroxysteroid sulfotransferase (SULT2A1) gene expression in human Caco-2 cells. J Biochem Mol Toxicol 28:32-8
Zhou, Tianyan; Huang, Chaoqun; Chen, Yue et al. (2013) Methamphetamine regulation of sulfotransferase 1A1 and 2A1 expression in rat brain sections. Neurotoxicology 34:212-8
Chen, Yue; Zhang, Shunfen; Zhou, Tianyan et al. (2013) Liver X receptor alpha mediated genistein induction of human dehydroepiandrosterone sulfotransferase (hSULT2A1) in Hep G2 cells. Toxicol Appl Pharmacol 268:106-12
Zhou, Tianyan; Chen, Yue; Huang, Chaoqun et al. (2012) Caffeine induction of sulfotransferases in rat liver and intestine. J Appl Toxicol 32:804-9
Tyapochkin, Eduard; Kumar, Vidya Prasanna; Cook, Paul F et al. (2011) Reaction product affinity regulates activation of human sulfotransferase 1A1 PAP sulfation. Arch Biochem Biophys 506:137-41
Huang, Chaoqun; Zhou, Tianyan; Chen, Yue et al. (2011) Estrogen-related receptor ERR?-mediated downregulation of human hydroxysteroid sulfotransferase (SULT2A1) in Hep G2 cells. Chem Biol Interact 192:264-71
Chen, Yue; Chen, Xinrong; Zhang, Shunfen et al. (2011) Influenza A virus infection activates cholesterol sulfotransferase (SULT2B1b) in the lung of female C57BL/6 mice. Biol Chem 392:869-76
Chen, Yue; Huang, Chaoqun; Zhou, Tianyan et al. (2010) Biochanin A induction of sulfotransferases in rats. J Biochem Mol Toxicol 24:102-14
Tyapochkin, Eduard; Cook, Paul F; Chen, Guangping (2009) para-Nitrophenyl sulfate activation of human sulfotransferase 1A1 is consistent with intercepting the E[middle dot]PAP complex and reformation of E[middle dot]PAPS. J Biol Chem 284:29357-64
Huang, C; Chen, Y; Zhou, T et al. (2009) Sulfation of dietary flavonoids by human sulfotransferases. Xenobiotica 39:312-22

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