Major ATPases on clofibrate-induced rat liver peroxisomes are not associated with 70 kDa peroxisomal membrane protein (PMP70)

J Biochem. 1992 Dec;112(6):733-6. doi: 10.1093/oxfordjournals.jbchem.a123967.

Abstract

We previously reported that novel Mg(2+)-ATPases were induced in rat liver peroxisomes by clofibrate administration and that these activities consisted of at least two types of enzymes, N-ethylmaleimide (NEM)-sensitive and -resistant. Here we present evidence that neither of these major peroxisomal ATPases is associated with the 70-kDa peroxisomal membrane protein (PMP70), because: (i) proteinase K treatment of peroxisomes resulted in inactivation of only NEM-sensitive ATPase, whereas disappeared PMP70 completely; (ii) NEM-sensitive ATPase activity was barely immunoprecipitated with anti-PMP70 IgG; (iii) the solubilized ATPases behaved differently from PMP70 on native PAGE; and finally (iv), the major peroxisomal ATPases were separated from PMP70 on gel filtration chromatography.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphatases / isolation & purification
  • Adenosine Triphosphatases / metabolism*
  • Animals
  • Ca(2+) Mg(2+)-ATPase / isolation & purification
  • Ca(2+) Mg(2+)-ATPase / metabolism
  • Chromatography, Gel
  • Clofibrate / pharmacology*
  • Electrophoresis, Polyacrylamide Gel
  • Ethylmaleimide / pharmacology
  • Liver / drug effects
  • Liver / metabolism*
  • Male
  • Membrane Proteins / isolation & purification
  • Membrane Proteins / metabolism*
  • Microbodies / drug effects
  • Microbodies / metabolism*
  • Rats
  • Rats, Wistar

Substances

  • Membrane Proteins
  • Adenosine Triphosphatases
  • Ca(2+) Mg(2+)-ATPase
  • Clofibrate
  • Ethylmaleimide