Purification and characterization of a cytosolic protein enhancing GSH-dependent microsomal iodothyronine 5'-monodeiodination

J Biol Chem. 1985 May 25;260(10):6012-9.

Abstract

A protein has been purified from rat liver cytosol which promoted GSH-responsive iodothyronine 5'-deiodinase activities in rat kidney microsomes. The factor behaved as a basic protein with an Mr of 11,000. It was active as a GSH-disulfide transhydrogenase with beta-hydroxyethyl disulfide as an acceptor and was also active in stimulating calf thymus ribonucleotide reductase with one-third the potency of native calf thymus glutaredoxin. Another basic protein, which degraded iodothyronines oxidatively, was also identified in the cytosolic preparations; this co-purified with soluble protein factor in the earlier purification stages and was partially separated from this factor by CM-cellulose chromatography. The glutaredoxin-like protein present in rat liver and kidney cytosol could provide a physiologic regulatory mechanism for GSH-dependent 5'-monodeiodination of iodothyronines.

Publication types

  • Comparative Study
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Cytosol / metabolism
  • Enzyme Activation / drug effects
  • Glutaredoxins
  • Glutathione / pharmacology*
  • Iodide Peroxidase / metabolism*
  • Kidney / metabolism
  • Male
  • Microsomes / metabolism
  • Oxidoreductases*
  • Peroxidases / metabolism*
  • Protein Disulfide Reductase (Glutathione) / metabolism
  • Proteins / isolation & purification*
  • Proteins / pharmacology
  • Rats
  • Thioredoxin-Disulfide Reductase / pharmacology
  • Thioredoxins / pharmacology

Substances

  • Glutaredoxins
  • Proteins
  • Thioredoxins
  • Oxidoreductases
  • Peroxidases
  • Iodide Peroxidase
  • Thioredoxin-Disulfide Reductase
  • Protein Disulfide Reductase (Glutathione)
  • Glutathione