The Preparation of Nucleotide-Protein Conjugates: Carbodiimides as Coupling Agents

  • Halloran M
  • Parker C
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Abstract

For some time it has been apparent that antibodies might be useful in the study of the fine structure of RNA and DNA. A major stumbling block has been the unavailability of a method which would render polynucleotides antigenic yet largely preserve their structural integrity. In approaching the problem of covalently conjugating polynucleotides to proteins as a means of stimulating antibody formation, we sought a procedure which would employ terminal nucleotide PO4 or OH groups for coupling. Two ways in which the terminal PO4 groups might be coupled covalently to protein would involve formation of a phosphodiester bond with protein seryl and threonyl residues or an N-P bond with protein ε-amino groups (Fig. 1, reactions 1 and 2 respectively). On the other hand, the OH group of a terminal sugar residue could react with protein carboxyl groups forming an ester (Fig. 1, reaction 3).

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Halloran, M. J., & Parker, C. W. (1966). The Preparation of Nucleotide-Protein Conjugates: Carbodiimides as Coupling Agents. The Journal of Immunology, 96(3), 373–378. https://doi.org/10.4049/jimmunol.96.3.373

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