Biosynthesis of rat renal gamma-glutamyl transpeptidase. Evidence for a common precursor of the two subunits

J Biol Chem. 1982 Jan 25;257(2):585-8.

Abstract

Rat kidney gamma-glutamyl transpeptidase is an amphipathic heterodimer, anchored to the lumenal surface of brush-border membranes via the NH2-terminal portion of its heavy subunit. The Mr values of the two subunits of detergent-solubilized enzyme are approximately 51,000 (heavy) and 22,000 (light), respectively. Biosynthesis of transpeptidase was studied in renal slices incubated with L-[35S]methionine. Transpeptidase-related proteins were isolated by immunoprecipitation with anti-transpeptidase antibodies. The major species seen after relatively short pulse times is a 78,000-dalton protein. Immunological characterization, kinetic, and pulse-chase studies indicate that the Mr = 78,000 species is the precursor of the two subunits of the enzyme. Like the dimeric enzyme, the Mr = 78,000 species contains both the core and the peripheral sugar, fucose, on its oligosaccharide moieties. Since, only the labeled dimeric enzyme appears in the brush-border membranes, conversion of the Mr = 78,000 species to the two subunits presumably occurs after its arrival at the Golgi but before its transport to the brush-border surface.

Publication types

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

MeSH terms

  • Animals
  • Kidney Cortex / enzymology*
  • Kinetics
  • Macromolecular Substances
  • Male
  • Methionine
  • Molecular Weight
  • Rats
  • Rats, Inbred Strains
  • Sulfur Radioisotopes
  • gamma-Glutamyltransferase / biosynthesis*

Substances

  • Macromolecular Substances
  • Sulfur Radioisotopes
  • Methionine
  • gamma-Glutamyltransferase