Characterization of a cleavage product in the human choriogonadotropin beta-subunit

Biochem Biophys Res Commun. 1988 Jul 29;154(2):626-32. doi: 10.1016/0006-291x(88)90185-4.

Abstract

The various molecular forms of human chorionic gonadotropin present in a crude preparation of urine from pregnant women were analyzed by two-dimensional gel electrophoresis and immunoblotting with monoclonal antibodies directed to synthetic peptides corresponding to the carboxyl-terminal part of either the alpha or beta-subunit. Under reducing conditions, immunoblotting with antibodies directed to the beta-subunit revealed the presence of a low-molecular-weight material of 22 kDa. This molecular form had large heterogeneity, as analyzed by isoelectrofocusing; it was immunoreactive with antibodies directed to the 111-145 region. Using microsequencing techniques, we found that the fragment had a NH2 terminal portion corresponding to the sequence of the beta-subunit appearing from residue 48. Thus, the 22-kDa fragment comprises the 48-145 portion of the beta-subunit and is probably a cleavage product of the native protein with intrachain nicking.

MeSH terms

  • Amino Acid Sequence
  • Antibodies, Monoclonal
  • Chorionic Gonadotropin / analysis*
  • Chorionic Gonadotropin, beta Subunit, Human
  • Electrophoresis, Polyacrylamide Gel
  • Female
  • Humans
  • Luteinizing Hormone / analysis
  • Peptide Fragments / analysis*
  • Pregnancy

Substances

  • Antibodies, Monoclonal
  • Chorionic Gonadotropin
  • Chorionic Gonadotropin, beta Subunit, Human
  • Peptide Fragments
  • Luteinizing Hormone