Literature DB >> 26062463

Cytochrome c adducts with PCB quinoid metabolites.

Miao Li1,2, Lynn M Teesch3, Daryl J Murry1,4, R Marshal Pope5, Yalan Li5, Larry W Robertson1,2, Gabriele Ludewig6,7.   

Abstract

Polychlorinated biphenyls (PCBs) are a group of 209 individual congeners widely used as industrial chemicals. PCBs are found as by-products in dye and paint manufacture and are legacy, ubiquitous, and persistent as human and environmental contaminants. PCBs with fewer chlorine atoms may be metabolized to hydroxy- and dihydroxy-metabolites and further oxidized to quinoid metabolites both in vitro and in vivo. Specifically, quinoid metabolites may form adducts on nucleophilic sites within cells. We hypothesized that the PCB-quinones covalently bind to cytochrome c and, thereby, cause defects in the function of cytochrome c. In this study, synthetic PCB quinones, 2-(4'-chlorophenyl)-1,4-benzoquinone (PCB3-pQ), 4-4'-chlorophenyl)-1,2-benzoquinone (PCB3-oQ), 2-(3', 5'-dichlorophenyl)-1,4-benzoquinone, 2-(3',4', 5'-trichlorophenyl)-1,4-benzoquinone, and 2-(4'-chlorophenyl)-3,6-dichloro-1,4-benzoquinone, were incubated with cytochrome c, and adducts were detected by liquid chromatography-mass spectrometry (LC-MS) and matrix-assisted laser desorption/ionization time of flight mass spectrometry (MALDI TOF). Sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) was employed to separate the adducted proteins, while trypsin digestion and liquid chromatography-tandem mass spectrometry (LC-MS/MS) were applied to identify the amino acid binding sites on cytochrome c. Conformation change of cytochrome c after binding with PCB3-pQ was investigated by SYBYL-X simulation and cytochrome c function was examined. We found that more than one molecule of PCB-quinone may bind to one molecule of cytochrome c. Lysine and glutamic acid were identified as the predominant binding sites. Software simulation showed conformation changes of adducted cytochrome c. Additionally, cross-linking of cytochrome c was observed on the SDS-PAGE gel. Cytochrome c was found to lose its function as electron acceptor after incubation with PCB quinones. These data provide evidence that the covalent binding of PCB quinone metabolites to cytochrome c may be included among the toxic effects of PCBs.

Entities:  

Keywords:  4-Chlorobiphenyl; Cytochrome c; Post-translational modification; Protein adducts; Protein cross-linking; Quinoid metabolites

Mesh:

Substances:

Year:  2015        PMID: 26062463      PMCID: PMC4676959          DOI: 10.1007/s11356-015-4801-3

Source DB:  PubMed          Journal:  Environ Sci Pollut Res Int        ISSN: 0944-1344            Impact factor:   4.223


  60 in total

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Journal:  Nat Protoc       Date:  2006       Impact factor: 13.491

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Authors:  Béatrice Lauby-Secretan; Dana Loomis; Yann Grosse; Fatiha El Ghissassi; Véronique Bouvard; Lamia Benbrahim-Tallaa; Neela Guha; Robert Baan; Heidi Mattock; Kurt Straif
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Journal:  Chem Res Toxicol       Date:  2002-04       Impact factor: 3.739

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Journal:  Proc Natl Acad Sci U S A       Date:  2009-06-02       Impact factor: 11.205

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Journal:  Chem Res Toxicol       Date:  2009-01       Impact factor: 3.739

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Journal:  Chem Res Toxicol       Date:  1993 Jul-Aug       Impact factor: 3.739

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Authors:  L M Geren; F Millett
Journal:  J Biol Chem       Date:  1981-05-25       Impact factor: 5.157

9.  Rates and Routes of Transport of PCBs in the Environment.

Authors:  I C Nisbet; A F Sarofim
Journal:  Environ Health Perspect       Date:  1972-04       Impact factor: 9.031

10.  Inadvertent polychlorinated biphenyls in commercial paint pigments.

Authors:  Dingfei Hu; Keri C Hornbuckle
Journal:  Environ Sci Technol       Date:  2010-04-15       Impact factor: 9.028

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3.  Characterization of the Metabolic Pathways of 4-Chlorobiphenyl (PCB3) in HepG2 Cells Using the Metabolite Profiles of Its Hydroxylated Metabolites.

Authors:  Chun-Yun Zhang; Susanne Flor; Patricia Ruiz; Gabriele Ludewig; Hans-Joachim Lehmler
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