Analysis of the Mi-2 autoantigen of dermatomyositis

Arthritis Rheum. 1995 Jan;38(1):123-8. doi: 10.1002/art.1780380119.

Abstract

Objective: To determine the biochemical structure and antigenic components of Mi-2 autoantigen, the target of autoantibodies in 15-20% of dermatomyositis patients.

Methods: Immunoprecipitation from 35S-labeled HeLa cell extract, immunoblotting, and purification from bovine thymus by immunoaffinity chromatography.

Results: All 46 sera that had anti-Mi-2 autoantibodies demonstrated by immunodiffusion immunoprecipitated a major protein of approximately 240 kd. Additional proteins of 200, 150, 72, 65, 63, 50, and 34 kd appeared to be part of the antigen. Fractions of purified bovine Mi-2 with antigenic activity showed high molecular weight bands comparable with immunoprecipitated HeLa Mi-2. Twenty-four of 47 anti-Mi-2 positive sera reacted with the 240-kd protein by immunoblot against anti-Mi-2 immunoprecipitates.

Conclusion: Mi-2 antigen consists of multiple proteins, of which the 240-kd protein appears to be the major reactive component.

Publication types

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

MeSH terms

  • Adenosine Triphosphatases*
  • Antigens / chemistry
  • Autoantibodies / immunology*
  • Autoantigens / blood
  • Autoantigens / chemistry
  • Autoantigens / isolation & purification
  • DNA Helicases*
  • Dermatomyositis / blood*
  • Dermatomyositis / immunology
  • Humans
  • Immunoblotting
  • Mi-2 Nucleosome Remodeling and Deacetylase Complex
  • Molecular Weight
  • Precipitin Tests
  • Proteins / analysis

Substances

  • Antigens
  • Autoantibodies
  • Autoantigens
  • CHD4 protein, human
  • Mi-2 antibodies
  • Proteins
  • Mi-2 Nucleosome Remodeling and Deacetylase Complex
  • Adenosine Triphosphatases
  • DNA Helicases