Conversion of covalently mercurated nucleic acids to tritiated and halogenated derivatives
Open Access
- 1 June 1975
- journal article
- research article
- Published by Oxford University Press (OUP) in Nucleic Acids Research
- Vol. 2 (6) , 915-930
- https://doi.org/10.1093/nar/2.6.915
Abstract
Mercurated nucleic acids are converted to the corresponding tritiated, brominated, and iodinated derivatives by treatment with sodium borotritlide, N-bromosuccinimide, and elemental iodine, respectively. All three reactions occur under mild conditions in neutral aqueous solutions. Mercury-halogen conversions are essentially quantitative at both the monoand polynucleotide levels. Tritlation reactions also proceed efficiently with mononucleotides, although polymers undergo incomplete demercuration. In spite of the latter limitation, these reactions provide novel and efficient synthetic routes to radio labeled nucleic acid derivatives.Keywords
This publication has 6 references indexed in Scilit:
- The Synthesis and Enzymatic Polymerization of Nucleotides Containing Mercury: Potential Tools for Nucleic Acid Sequencing and Structural AnalysisProceedings of the National Academy of Sciences, 1973
- Iodination of nucleic acids in vitroBiochemistry, 1971
- Light-induced cross-linking of DNA in the presence of a furocoumarin (psoralen): Studies with phage λ, Escherichia coli, and mouse leukemia cellsBiochimica et Biophysica Acta (BBA) - Nucleic Acids and Protein Synthesis, 1970
- Protein purification by affinity chromatography. Derivatizations of agarose and polyacrylamide beads.1970
- Chemical modification of viral ribonucleic acid☆II. Bromination and iodinationBiochimica et Biophysica Acta, 1963
- Tissue sulfhydryl groupsArchives of Biochemistry and Biophysics, 1959