Localization of the proteinase-induced thiol groups in alpha 2-macroglobulin

Biochem Biophys Res Commun. 1983 Mar 29;111(3):964-9. doi: 10.1016/0006-291x(83)91394-3.

Abstract

Free thiol groups released on proteolytic attack of alpha 2-macroglobulin by trypsin or chymotrypsin bind covalently to thiopropyl-Sepharose, indicating that they are located at the surface of the complexes. These cysteine sulfhydryl groups appear to be in contact with the alpha 2M-bound proteases from singlet-singlet energy transfer measurements between fluorescein isothiocyanate-labeled proteinases and N-(iodoacetylaminoethyl)-5-naphtylamine-1-sulfonic acid-labeled thiols in alpha 2-macroglobulin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Binding Sites
  • Chromatography, Affinity
  • Chymotrypsin / metabolism
  • Endopeptidases / metabolism*
  • Energy Transfer
  • Humans
  • Protein Binding
  • Sulfhydryl Compounds / metabolism*
  • Surface Properties
  • Trypsin / metabolism
  • alpha-Macroglobulins / metabolism*

Substances

  • Sulfhydryl Compounds
  • alpha-Macroglobulins
  • Endopeptidases
  • Chymotrypsin
  • Trypsin