The detection of phospholipase-resistant and -sensitive glycosyl-phosphatidylinositol membrane anchors by western blotting

Anal Biochem. 1994 Jun;219(2):249-55. doi: 10.1006/abio.1994.1264.

Abstract

Glycosyl-phosphatidylinositol (GPI) membrane anchors are present on a large number of eukaryotic plasma membrane proteins. Some of these anchors can be cleaved with bacterial phosphatidylinositol-specific phospholipases C, and a glycosyl-phosphatidylinositol-specific phospholipase C from Trypanosoma brucei, to reveal an epitope called the cross-reacting determinant. Other glycosyl-phosphatidylinositol anchors are resistant to the action of these enzymes prior to treatment with mild base. A simple method is described for identifying both phospholipase-sensitive and -resistant anchors using anti-cross-reacting determinant antibodies on Western blots. This procedure represents a high-sensitivity general method for the identification of GPI-anchored proteins.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Western / methods*
  • Cell Membrane / metabolism
  • Electrophoresis, Polyacrylamide Gel / methods
  • Epitopes / analysis
  • Glycosylphosphatidylinositols / analysis*
  • Glycosylphosphatidylinositols / metabolism
  • Molecular Structure
  • Phosphatidylinositol Diacylglycerol-Lyase
  • Phosphoric Diester Hydrolases / metabolism*
  • Structure-Activity Relationship
  • Substrate Specificity
  • Trypanosoma brucei brucei / enzymology
  • Type C Phospholipases / metabolism*

Substances

  • Epitopes
  • Glycosylphosphatidylinositols
  • Phosphoric Diester Hydrolases
  • Type C Phospholipases
  • Phosphatidylinositol Diacylglycerol-Lyase