Structural characterization of a recombinant CD4-IgG hybrid molecule

Eur J Biochem. 1990 Dec 12;194(2):611-20. doi: 10.1111/j.1432-1033.1990.tb15660.x.

Abstract

CD4-IgG is a homodimer of a hybrid polypeptide consisting of the two amino-terminal domains (residues 1-180) of human CD4 fused to the hinge region and the second and third constant-sequence (CH2 and CH3) Fc domains (residues 216-441) of human immunoglobulin G (IgG-1). This antibody-like molecule, termed an immunoadhesin, was produced in an effort to combine the binding specificity of CD4 with several potentially desirable properties of IgG molecules [Capon et al. (1989) Nature 337, 525-531]. The structural characteristics of the molecule have been evaluated to demonstrate that CD4-IgG has the same features as the N-terminal region of soluble CD4, while retaining those expected for the Fc portion of human IgG. Identification of peptides recovered from the tryptic map confirmed 98.8% of the expected structure of CD4-IgG. The detection of glucosamine in peptides containing Asn257 and the retention time shift of this tryptic peptide after deglycosylation confirmed the presence of Asn-linked oligosaccharides at this position. Four pairs of intrachain and two interchain disulfide bonds were also established.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • CD4 Antigens / genetics*
  • Chromatography, High Pressure Liquid
  • Cricetinae
  • Cricetulus
  • Humans
  • Immunoglobulin G / genetics*
  • Mass Spectrometry
  • Molecular Sequence Data
  • Peptide Mapping
  • Sulfhydryl Compounds
  • Trypsin

Substances

  • CD4 Antigens
  • Immunoglobulin G
  • Sulfhydryl Compounds
  • Trypsin

Associated data

  • GENBANK/UNKNOWN