Purification and characterization of genetically polymorphic deoxyribonuclease I from human kidney

J Biochem. 1991 Sep;110(3):321-3. doi: 10.1093/oxfordjournals.jbchem.a123578.

Abstract

Deoxyribonuclease I (DNase I) was purified about 850,000-fold from human kidney using a rabbit anti-human urine DNase I antibody and sensitive DNase I activity assay. On SDS-PAGE, the purified kidney DNase I gave a single major band, and its molecular mass was estimated to be 38,000 Da. The activity of purified kidney DNase I was dependent on the presence of Mg2+ and Ca2+. G-Actin inhibited the activity, as did the anti-urine DNase I antibody. The properties of the kidney DNase I were the same as those of urine DNase I.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / pharmacology
  • Adult
  • Chromatography, Gel / methods
  • Chromatography, Ion Exchange / methods
  • Deoxyribonuclease I / genetics
  • Deoxyribonuclease I / isolation & purification*
  • Deoxyribonuclease I / metabolism
  • Electrophoresis, Polyacrylamide Gel
  • Humans
  • Kidney / enzymology*
  • Kinetics
  • Male
  • Molecular Weight
  • Polymorphism, Genetic

Substances

  • Actins
  • Deoxyribonuclease I