Distribution of sulfhydryl groups in intestinal brush border membranes. Localization of side-chains essential for glucose transport and phlorizin binding

Biochim Biophys Acta. 1979 Dec 4;558(2):233-45. doi: 10.1016/0005-2736(79)90063-4.

Abstract

1. Brush border membrane vesicles from rabbit small intestine were found to contain 46 nmol SH groups/mg protein, 52% of which could react with 4,4'-dithiodipyridine, a membrane permeating probe. Only 18% of the total SH-groups reacted with the impermeant probe 5,5'-dithiobis(2-nitrobenzoic acid), indicating that only this fraction is externally located. 2. Brush border membrane vesicles could be disrupted by a gentle treatment with deoxycholate, releasing most of their electron-dense core material. In deoxycholate-treated vesicles most of the SH groups that reacted with 4,4'-dithiodipyridine react with 5,5'-dibiobis(2-nitrobenzoic acid), suggesting that both membrane surfaces became exposed to the extravesicular medium. 3. In intact vesicles (1.2 mg protein/ml), the binding of phlorizin (a competitive inhibitor of the monosaccharide transport system) was 50% inhibited by 67 microM of the penetrating organomercurial p-chloromercuribenzoate, but was about ten times less sensitive to the poorly permeating p-chloromercuriphenylsulfonate. In contrast, binding of phlorizin to leaky (deoxycholate-treated) membranes was equally susceptible to either reagent. 4. Mercurial inhibition of phlorizin binding could be reversed by dithioerythritol in both sealed and leaky membranes, whereas the less permeant thiol L-glutathione (reduced form) could only revert the inhibition in leaky membranes.

MeSH terms

  • Animals
  • Binding Sites
  • Biological Transport
  • Cell Membrane / analysis*
  • Chloromercuribenzoates / pharmacology
  • Deoxycholic Acid / pharmacology
  • Dithionitrobenzoic Acid / pharmacology
  • Dithiothreitol / pharmacology
  • Glucose / metabolism*
  • Intestinal Mucosa / ultrastructure
  • Microvilli / analysis*
  • Phlorhizin / metabolism*
  • Rabbits
  • Sulfhydryl Compounds / analysis*

Substances

  • Chloromercuribenzoates
  • Sulfhydryl Compounds
  • Deoxycholic Acid
  • Dithionitrobenzoic Acid
  • Phlorhizin
  • Glucose
  • Dithiothreitol