Phosphorylation of different human milk proteins by human catalytic secretory immunoglobulin A

Biochem Mol Biol Int. 1996 Jun;39(3):521-7. doi: 10.1080/15216549600201571.

Abstract

The ability of secretory immunoglobulin A (slgA) from milk of healthy mothers to phosphorylate various milk proteins in the presence of gamma-[32P]-ATP was shown to be a property of the antibodies. The polyclonal slgA was purified by sequential chromatography on Protein-A Sepharose and DEAE-cellulose, and then separated by chromatography on the ATP-Sepharose. The preparations containing all milk proteins except for protein kinases [integrated milk proteins (IMP)] were obtained by extraction of the kinase activities from the milk using their affinity to the insoluble crosslinked staphylococcus. Addition of slgA fractions (having a different affinity to ATP) to the IMP led to phosphorylation of casein and several other milk proteins with different efficiencies.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Antibodies, Catalytic / metabolism*
  • Caseins / metabolism
  • Chromatography, Affinity
  • Chromatography, Ion Exchange
  • DEAE-Cellulose
  • Electrophoresis, Polyacrylamide Gel
  • Female
  • Humans
  • Immunoglobulin A, Secretory / isolation & purification
  • Immunoglobulin A, Secretory / pharmacology*
  • Milk Proteins / metabolism*
  • Phosphorylation
  • Protein Kinases / isolation & purification
  • Protein Kinases / metabolism
  • Trypsin / metabolism

Substances

  • Antibodies, Catalytic
  • Caseins
  • Immunoglobulin A, Secretory
  • Milk Proteins
  • Adenosine Triphosphate
  • DEAE-Cellulose
  • Protein Kinases
  • Trypsin