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University of Iowa

Superfund Research Program

PCBs and Hydroxysteroid (Alcohol) Sulfotransferases

Project Leader: Michael W. Duffel
Co-Investigators: Larry W. Robertson, Hans-Joachim Lehmler
Grant Number: P42ES013661
Funding Period: 2006-2020
View this project in the NIH Research Portfolio Online Reporting Tools (RePORT)

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Project Summary (2010-2015)

Polychlorinated biphenyls (PCBs) are metabolized in humans and other mammals to hydroxylated derivatives (OHPCBs) that are increasingly recognized as having significant roles in the retention of, and toxic responses to, these environmental contaminants. OHPCBs interact with cytosolic sulfotransferases (SULTs) as substrates and inhibitors, and the effects of these interactions on the toxicities of these molecules depend upon the structure of the OHPCB and the isoform(s) of SULT involved. The long term goal of Dr. Duffel’s research is to better understand relationships between the regulation of catalytic function of SULTs and the biological activities of OHPCBs derived from semi-volatile PCBs. The primary objectives of the work are to:

  • Address gaps in the knowledge related to structure-activity relationships of OHPCBs with the family 2 (also known as hydroxysteroid or alcohol) SULTs,
  • Elucidate how the oxidative environments of both family 1 and family 2 SULTs regulate their interactions with OHPCBs, and
  • Understand the properties of the sulfuric acid esters of OHPCBs formed in SULT-catalyzed reactions.

Dr. Duffel’s central hypothesis is that OHPCBs serve as substrates and inhibitors of both family 1 and family 2 SULTs, and that the interactions of individual OHPCBs with these enzymes are significantly altered in a predictable manner by oxidation of thiols in these enzymes. Moreover, a corollary hypothesis is that the sulfated OHPCB-metabolites have toxicologically important chemical and biochemical properties. The specific aims to be investigated during the next five-year period are:

  1. to study the structure-activity relationships for OHPCBs as inhibitors and substrates of human hydroxysteroid sulfotransferase hSULT2A1;
  2. to explore the roles that the oxidation of thiols in SULTs play in regulation of their specificity for OHPCBs as inhibitors and substrates; and
  3. to understand the properties of the sulfuric acid esters derived from sulfation of OHPCBs.

This research yields significant new fundamental insight into the interactions of OHPCBs with SULTs, and the potential consequences of these interactions for sulfation of endogenous molecules as well as xenobiotics.

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