Binding of [1-14C]methyl isocyanate to erythrocyte membrane proteins

J Appl Toxicol. 1996 Mar-Apr;16(2):137-8. doi: 10.1002/(SICI)1099-1263(199603)16:2<137::AID-JAT317>3.0.CO;2-E.

Abstract

We describe the interaction of methyl isocyanate with reactive sulphydryl groups of rat erythrocyte membrane proteins. Intraperitoneal administration, as well as in vitro incubation of methyl isocyanate, caused a significant reduction in the free sulphydryl content of erythrocyte membrane proteins. [1-14C]Methyl isocyanate was specifically bound to band III of the erythrocyte membrane and caused the breakdown of band III proteins.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Anion Exchange Protein 1, Erythrocyte / analysis
  • Carbon Radioisotopes
  • Electrophoresis, Polyacrylamide Gel
  • Erythrocyte Membrane / metabolism*
  • Female
  • Isocyanates / metabolism*
  • Membrane Proteins / metabolism*
  • Rats
  • Rats, Wistar

Substances

  • Anion Exchange Protein 1, Erythrocyte
  • Carbon Radioisotopes
  • Isocyanates
  • Membrane Proteins
  • methyl isocyanate