Mechanism of IgM polymerization

Proc Natl Acad Sci U S A. 1974 Mar;71(3):657-61. doi: 10.1073/pnas.71.3.657.

Abstract

The stoichiometry of J chain in pentamer IgM has been determined by measuring the radiolabeled thiols in the constituent chains after complete reduction and alkylation of the polymer. One mole of J was found to be disulfide bonded to 1 mol of pentamer. The linkage of J chain in IgM has been determined by correlating the J disulfides cleaved with the subunits released after limited reduction and alkylation of the polymer. The analyses showed that: (a) Significant amounts of monomers, as well as small quantities of dimers, trimers, and tetramers, were generated by the reducing conditions employed. (b) The number of J disulfide bonds broken did not correspond to the extent of depolymerization. (c) No J disulfides were cleaved in the J-containing dimer products of the limited reduction. These data demonstrated that the J chain is located as a disulfide clasp between two of the IgM monomer subunits. From the observed linkage, the assembly of IgM is postulated to proceed by a series of sequential disulfide exchanges beginning with the formation of the J-containing dimer.

MeSH terms

  • Alkylation
  • Carbon Radioisotopes
  • Chemical Phenomena
  • Chemistry
  • Cysteine / analysis
  • Cystine / analysis
  • Dithiothreitol
  • Electrophoresis, Polyacrylamide Gel
  • Humans
  • Immunoglobulin J-Chains
  • Immunoglobulin M / analysis*
  • Iodoacetates
  • Oxidation-Reduction
  • Polymers
  • Tritium

Substances

  • Carbon Radioisotopes
  • Immunoglobulin J-Chains
  • Immunoglobulin M
  • Iodoacetates
  • Polymers
  • Tritium
  • Cystine
  • Cysteine
  • Dithiothreitol