Biotinyl-estradiol derivatives in enzyme immunoassays: structural requirements for optimal antibody binding

J Steroid Biochem. 1990 May;35(6):633-9. doi: 10.1016/0022-4731(90)90302-9.

Abstract

The use of the avidin/biotin complex in immunoassays is well documented. No comprehensive studies, however, are available on the structural requirements of the linkage between biotin and small molecules to get an optimal antigen-antibody interaction. We have synthesized seven different biotinylated estradiol derivatives. They were evaluated in an antibody- and in an antigen-immobilized enzyme immunoassay system. All three derivatives lacking a spacer group were useless for use in immunoassays, demonstrating the importance of a long distance between the biotin- and estradiol-moiety. In addition, the chemical structure of the linkage at the site of attachment to the steroid skeleton is very important for the antibody recognition: it may either be rigid but identical to that one used in the immunogen (6-carboxymethyloxime), or must be structurally flexible as exemplified by a 6-amido-linkage. A rigid structure (hydrazone) different from that of the immunogen absolutely prevents antibody binding.

MeSH terms

  • Antigen-Antibody Reactions*
  • Biotin / analogs & derivatives*
  • Biotin / immunology
  • Chemical Phenomena
  • Chemistry
  • Chromatography, High Pressure Liquid
  • Estradiol / analogs & derivatives
  • Estradiol / immunology*
  • Immunoenzyme Techniques*
  • Structure-Activity Relationship

Substances

  • Estradiol
  • Biotin