Covalent attachment of DNA to agarose. Improved synthesis and use in affinity chromatography

Eur J Biochem. 1975 Jun;54(2):411-8. doi: 10.1111/j.1432-1033.1975.tb04151.x.

Abstract

DNA has been covalently linked to insoluble matrices of agarose (Sepharose) in high yield using cyanogen bromide activation. Both double-stranded and single-stranded DNA have been coupled with yields up to 225 nmol/mg dry weight Sepharose or 3-8 mumol nucleotide phosphate/ml bed volume. The DNA-Sepharose has been used for (a) the affinity chromatography of various enzymes (Escherichia coli DNA polymerase I and RNA polymerase) from crude extracts or after initial purification steps, resulting in high yields and degrees of purification, and for (b) nucleic acid hybridization. The DNA-Sepharose is stable to high temperature, prolonged storage, and in the case of single-stranded DNA, can be washed with NaOH to destroy nuclease activity and to release any digested oligonucleotides or mononucleotides.

MeSH terms

  • Animals
  • Binding Sites
  • Cattle
  • Chromatography, Affinity / methods*
  • Cyanogen Bromide
  • DNA Nucleotidyltransferases / isolation & purification
  • DNA*
  • DNA-Directed RNA Polymerases / isolation & purification
  • Drug Stability
  • Escherichia coli / enzymology
  • Kinetics
  • Nucleic Acid Denaturation
  • Nucleic Acid Hybridization
  • Polysaccharides*
  • Sepharose*
  • Temperature
  • Thymus Gland
  • Time Factors

Substances

  • Polysaccharides
  • DNA
  • Sepharose
  • DNA Nucleotidyltransferases
  • DNA-Directed RNA Polymerases
  • Cyanogen Bromide