Demonstration of GTP-binding proteins and ADP-ribosylated proteins in rat liver Golgi fraction

Biochem Biophys Res Commun. 1989 Oct 16;164(1):333-8. doi: 10.1016/0006-291x(89)91722-1.

Abstract

A Golgi-rich fraction isolated from rat liver was found to contain GTP-binding proteins with 20-25 kDa, which were tightly bound to the Golgi membrane. The Golgi fraction also contained two species of proteins which were ADP-ribosylated by bacterial toxins. Protein(s) which was ADP-ribosylated by botulinum toxin had a similar molecular mass as those with GTP-binding activity but was easily released from the membrane. Another protein with 46 kDa which was ADP-ribosylated by pertussis toxin was tightly bound to the membrane but had no significant GTP-binding activity under conditions tested here. These proteins were much less or negligible in the plasma membrane and the endoplasmic reticulum.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Botulinum Toxins / metabolism
  • Electrophoresis, Polyacrylamide Gel
  • GTP-Binding Proteins / metabolism*
  • Golgi Apparatus / metabolism*
  • Liver / metabolism*
  • Nucleoside Diphosphate Sugars / metabolism*
  • Pertussis Toxin
  • Poly Adenosine Diphosphate Ribose / metabolism*
  • Proteins / metabolism*
  • Rats
  • Rats, Inbred Strains
  • Virulence Factors, Bordetella / metabolism

Substances

  • Nucleoside Diphosphate Sugars
  • Proteins
  • Virulence Factors, Bordetella
  • Poly Adenosine Diphosphate Ribose
  • Pertussis Toxin
  • Botulinum Toxins
  • GTP-Binding Proteins