Rapid affinity purification of retinal arrestin (48 kDa protein) via its light-dependent binding to phosphorylated rhodopsin

FEBS Lett. 1986 Oct 27;207(2):292-5. doi: 10.1016/0014-5793(86)81507-1.

Abstract

Arrestin (also named '48 kDa protein' or 'S-antigen') is a soluble protein involved in controlling light-dependent cGMP phosphodiesterase activity in retinal rods, and is also known for its ability to induce autoimmune uveitis of the eye. We report a rapid and simple purification method based on the property of arrestin to bind specifically and reversibly to illuminated and phosphorylated rhodopsin [(1984) FEBS Lett. 176, 473-478]. This method does not require column chromatography and yields about 2-4 mg purified arrestin from 15 bovine retinas. Pure arrestin can be resolved by isoelectric focusing into at least 10 distinct bands, all of which stain with a monoclonal antibody specific for S-antigen.

Publication types

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

MeSH terms

  • Animals
  • Antigens / isolation & purification*
  • Antigens / metabolism
  • Arrestin
  • Cattle
  • Centrifugation
  • Chromatography
  • Chromatography, High Pressure Liquid
  • Eye Proteins / isolation & purification*
  • Eye Proteins / metabolism
  • Isoelectric Focusing
  • Light*
  • Phosphorylation
  • Retina / analysis*
  • Retinal Pigments / metabolism*
  • Rhodopsin / metabolism*
  • Rhodopsin / radiation effects

Substances

  • Antigens
  • Arrestin
  • Eye Proteins
  • Retinal Pigments
  • Rhodopsin