Home LiteratureArticle Details
PMID: 12167474 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S. Review

Toxic, halogenated cysteine S-conjugates and targeting of mitochondrial enzymes of energy metabolism.

Biochemical pharmacology ·Vol. 64 ·No. 4 ·2002-08-15 ·Pages 553-64

Cooper AJ, Bruschi SA, Anders MW

Abstract

Several haloalkenes are metabolized in part to nephrotoxic cysteine S-conjugates; for example, trichloroethylene and tetrafluoroethylene are converted to S-(1,2-dichlorovinyl)-L-cysteine (DCVC) and S-(1,1,2,2-tetrafluoroethyl)-L-cysteine (TFEC), respectively. Although DCVC-induced toxicity has been investigated since the 1950s, the toxicity of TFEC and other haloalkene-derived cysteine S-conjugates has been studied more recently. Some segments of the US population are exposed to haloalkenes either through drinking water or in the workplace. Therefore, it is important to define the toxicological consequences of such exposures. Most halogenated cysteine S-conjugates are metabolized by cysteine S-conjugate beta-lyases to pyruvate, ammonia, and an alpha-chloroenethiolate (with DCVC) or an alpha-difluoroalkylthiolate (with TFEC) that may eliminate halide to give a thioacyl halide, which reacts with epsilon-amino groups of lysine residues in proteins. Nine mammalian pyridoxal 5'-phosphate (PLP)-containing enzymes catalyze cysteine S-conjugate beta-lyase reactions, including mitochondrial aspartate aminotransferase (mitAspAT), and mitochondrial branched-chain amino acid aminotransferase (BCAT(m)). Most of the cysteine S-conjugate beta-lyases are syncatalytically inactivated. TFEC-induced toxicity is associated with covalent modification of several mitochondrial enzymes of energy metabolism. Interestingly, the alpha-ketoglutarate- and branched-chain alpha-keto acid dehydrogenase complexes (KGDHC and BCDHC), but not the pyruvate dehydrogenase complex (PDHC), are susceptible to inactivation. mitAspAT and BCAT(m) may form metabolons with KGDHC and BCDHC, respectively, but no PLP enzyme is known to associate with PDHC. Consequently, we hypothesize that not only do these metabolons facilitate substrate channeling, but they also facilitate toxicant channeling, thereby promoting the inactivation of proximate mitochondrial enzymes and the induction of mitochondrial dysfunction.

MeSH Terms
Animals Carbon-Sulfur Lyases/metabolism Cysteine/analogs & derivatives,toxicity Energy Metabolism/drug effects Humans Hydrocarbons, Fluorinated/toxicity Lyases/metabolism Mitochondria/drug effects,enzymology Pyridoxal Phosphate/metabolism
Chemicals
Hydrocarbons, Fluorinated Pyridoxal Phosphate S-(1,2-dichlorovinyl)cysteine S-(1,1,2,2-tetrafluoroethyl)cysteine Lyases Carbon-Sulfur Lyases selenocysteine lyase S-alkylcysteine lyase Cysteine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Cooper Arthur J L
Department of Biochemistry, Weill Medical College of Cornell University, New York, NY 10021, USA. [email protected]
Bruschi Sam A
Anders M W
Article Info
Journal
Biochemical pharmacology
Abbr.
Biochem Pharmacol
ISSN
0006-2952
Published
2002-08-15
Pages
553-64
Language
English
Region
England
NLM ID
0101032
Subset
IM
Grants
NIA NIH HHS · AG14930 · United States
NIEHS NIH HHS · ES03127 · United States
NIEHS NIH HHS · ES07033 · United States
NIEHS NIH HHS · ES08421 · United States
NIGMS NIH HHS · R29 GM5196 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]