The roles of carbohydrate chains of the beta-subunit on the functional expression of gastric H(+),K(+)-ATPase

J Biol Chem. 2000 Mar 24;275(12):8324-30. doi: 10.1074/jbc.275.12.8324.

Abstract

Gastric H(+),K(+)-ATPase consists of alpha and beta-subunits. The alpha-subunit is the catalytic subunit, and the beta-subunit is a glycoprotein stabilizing the alpha/beta complex in the membrane as a functional enzyme. There are seven putative N-glycosylation sites on the beta-subunit. In this study, we examined the roles of the carbohydrate chains of the beta-subunit by expressing the alpha-subunit together with the beta-subunit in which one, several, or all of the asparagine residues in the N-glycosylation sites were replaced by glutamine. Removing any one of seven carbohydrate chains from the beta-subunit retained the H(+),K(+)-ATPase activity. The effects of a series of progressive removals of carbohydrate chains on the H(+),K(+)-ATPase activity were cumulative, and removal of all carbohydrate chains resulted in the complete loss of H(+), K(+)-ATPase activity. Removal of any single carbohydrate chain did not affect the alpha/beta assembly; however, little alpha/beta assembly was observed after removal of all the carbohydrate chains from the beta-subunit. In contrast, removal of three carbohydrate chains inhibited the surface delivery of the beta-subunit and the alpha-subunit assembled with the beta-subunit, indicating that the surface delivery mechanism is more dependent on the carbohydrate chains than the expression of the H(+),K(+)-ATPase activity and alpha/beta assembly.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • COS Cells
  • Cell Compartmentation
  • Gastric Mucosa / enzymology*
  • Gene Expression Regulation, Enzymologic
  • Glycoproteins / genetics
  • Glycoproteins / metabolism*
  • Glycosylation
  • H(+)-K(+)-Exchanging ATPase / genetics
  • H(+)-K(+)-Exchanging ATPase / metabolism*
  • Models, Molecular
  • Protein Processing, Post-Translational
  • Protein Structure, Tertiary
  • Rabbits
  • Recombinant Proteins / metabolism

Substances

  • Glycoproteins
  • Recombinant Proteins
  • H(+)-K(+)-Exchanging ATPase