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From the Immunology Division, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri
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
-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).
Footnotes
1 Postdoctoral Fellow of the United States Public Health Service, Grant 2 T1-AI-219.
2 Recipient of a Research Career Development Award from the United States Public Health Service.
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