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PMID: 11714719 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Membrane association of glutathione S-transferase mGSTA4-4, an enzyme that metabolizes lipid peroxidation products.

The Journal of biological chemistry ·Vol. 277 ·No. 6 ·2002-02-08 ·Pages 4232-9

Singh SP, Janecki AJ, Srivastava SK, Awasthi S, Awasthi YC, Xia SJ, Zimniak P

Abstract

Lipid peroxidation products have signaling functions and at higher concentrations are toxic and may trigger cell death. The compounds are metabolized predominantly by glutathione S-transferases exemplified by mGSTA4-4, an enzyme highly efficient in glutathione conjugation of 4-hydroxyalkenals, and possessing glutathione peroxidase activity toward phospholipid hydroperoxides. mGSTA4-4 belongs to the predominant group of "canonical" glutathione S-transferases that are soluble and generally localized in the cytoplasm. The intracellular localization of mGSTA4-4 was examined in hepatocytes of normal mouse liver and in transfected HepG2 cells by fluorescence microscopy and digital deconvolution. mGSTA4-4 was found to be predominantly localized at or near the plasma membrane in transfected HepG2 cells, as well as in hepatocytes endogenously expressing the protein. In vitro, mGSTA4-4 associated with liposomes, and this interaction was potentiated when the liposomes contained negatively charged phospholipids. Mutating lysine 115 to glutamic acid resulted in a loss of the plasma membrane targeting of mGSTA4-4 as well as in a significant reduction of its binding to liposomes in vitro. These data suggest preferential targeting of mGSTA4-4 to the plasma membrane that may contain the major substrate(s) for this enzyme. Lysine 115 is critically important for the membrane association of mGSTA4-4, most likely by entering into an electrostatic interaction with negatively charged phospholipid headgroups.

MeSH Terms
Animals Cell Line Cell Membrane/enzymology Glutathione Transferase/metabolism Hepatocytes/enzymology Lipid Peroxidation Liposomes Mice Mutagenesis, Site-Directed Phosphatidylcholines Phospholipids/metabolism Subcellular Fractions/enzymology Transfection
Chemicals
Liposomes Phosphatidylcholines Phospholipids asolectin Glutathione Transferase leukotriene-C4 synthase
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Singh Sharda P
Department of Internal Medicine, University of Arkansas for Medical Sciences, and Central Arkansas Veterans Healthcare System, Little Rock, Arkansas 72205, USA.
Janecki Andrzej J
Srivastava Sanjay K
Awasthi Sanjay
Awasthi Yogesh C
Xia Shujuan J
Zimniak Piotr
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
2002-02-08
Epub
2001-00-19
Pages
4232-9
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NCI NIH HHS · CA27967 · United States
NCI NIH HHS · CA77495 · United States
NIEHS NIH HHS · ES07804 · United States
NEI NIH HHS · EY04396 · United States
NIDDK NIH HHS · K08-DK02557 · United States
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