Cytochrome p-450-mediated differential oxidative modification of proteins: albumin, apolipoprotein E, and CYP2E1 as targets

J Toxicol Environ Health A. 2004 Dec;67(23-24):2061-71. doi: 10.1080/15287390490514895.

Abstract

Although many studies established a role of cytochrome P-450s in metabolism of xenobiotics, few studies evaluating the ability of cytochrome P-450s to oxidize proteins have been reported. The ability of cytochrome P-450s to induce oxidative modification of albumin, apolipoprotein E, and CYP2E1 protein was investigated. Microsomal cytochrome P-450s induced production of reactive radical species, leading to differential modification of the proteins. Albumin remained unmodified, and CYP2E1 protein was degraded, whereas recombinant and endogenous apolipoprotein E was aggregated. The modification of apolipoprotein E was isoform independent. Cytochrome P-450 inhibitors or antioxidants inhibited the production of reactive radical species and protein modification. These results demonstrate that response of each protein to cytochrome P-450-mediated oxidative attack is different, and cytochrome P-450s can induce apolipoprotein E aggregation, a process that might be relevant to accumulation of altered protein in various abnormal conditions. In view of the ubiquitous expression of cytochrome P-450s, the present results may have important toxicological implications.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Albumins / metabolism*
  • Animals
  • Apolipoproteins E / metabolism*
  • Cytochrome P-450 CYP2E1 / metabolism*
  • Cytochrome P-450 Enzyme System / pharmacology*
  • Escherichia coli
  • Isoenzymes
  • Male
  • Microsomes
  • Oxidative Stress*
  • Rats
  • Rats, Sprague-Dawley
  • Reactive Oxygen Species
  • Xenobiotics / metabolism*

Substances

  • Albumins
  • Apolipoproteins E
  • Isoenzymes
  • Reactive Oxygen Species
  • Xenobiotics
  • Cytochrome P-450 Enzyme System
  • Cytochrome P-450 CYP2E1