A photoactivable phospholipid analogue that specifically labels membrane cytoskeletal proteins of intact erythrocytes

Biochemistry. 1989 Aug 22;28(17):6943-9. doi: 10.1021/bi00443a025.

Abstract

A radioactive photoactivable analogue of phosphatidylethanolamine, 2-(2-azido-4-nitro-benzoyl)-1-acyl-sn-glycero-3-phospho[14C]ethanolamine ([14C]AzPE), was synthesized. Upon incubation with erythrocytes in the dark, about 90% of [14C]AzPE spontaneously incorporated into the cells; of this fraction, about 90% associated with the membrane, all of it noncovalently. Upon photoactivation, 3-4% of the membrane-associated probe was incorporated into protein. Analysis of this fraction by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, as well as extraction of labeled membranes with alkali or detergent, showed that the probe preferentially labeled cytoskeletal proteins. [14C]AzPE appears to be a useful tool for the study of lipid-protein interactions at the cytoplasmic face of the plasma membrane of intact cells.

Publication types

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

MeSH terms

  • Affinity Labels / metabolism*
  • Carbon Radioisotopes
  • Cytoskeletal Proteins / blood*
  • Cytoskeletal Proteins / isolation & purification
  • Erythrocyte Membrane / metabolism*
  • Humans
  • Indicators and Reagents
  • Kinetics
  • Membrane Proteins / blood*
  • Membrane Proteins / isolation & purification
  • Phosphatidylethanolamines / blood*
  • Phosphatidylethanolamines / chemical synthesis
  • Photolysis

Substances

  • Affinity Labels
  • Carbon Radioisotopes
  • Cytoskeletal Proteins
  • Indicators and Reagents
  • Membrane Proteins
  • Phosphatidylethanolamines
  • 2-(2-azido-4-nitrobenzoyl)-1-myristoylglycero-3-phosphoethanolamine