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Potent anti-tumor effects of an active site mutant of human manganese-superoxide dismutase: Evolutionary conservation of product inhibition

  • Christopher A. Davis
  • , Amy S. Hearn
  • , Bradley Fletcher
  • , Justin Bickford
  • , Jorge E. Garcia
  • , Vincent Leveque
  • , J. Andres Melendez
  • , David N. Silverman
  • , James Zucali
  • , Anupam Agarwal
  • , Harry S. Nick

Research output: Contribution to journalArticlepeer-review

42 Scopus citations

Abstract

Mn-SOD serves as the primary cellular defense against oxidative damage by converting superoxide radicals (O2.-) to O2 and H2O2. A unique characteristic of this mitochondrial anti-oxidant enzyme is the conservation from bacteria to man of a rapidly formed product inhibited state. Using site-directed mutagenesis, we have generated an active site mutant (H30N) of human Mn-SOD, which exhibits significantly reduced product inhibition and increased enzymatic efficiency. Overexpression of the H30N enzyme causes anti-proliferative effects in vitro and anti-tumor effects in vivo. Our results provide a teleological basis for the phylogenetically invariant nature of position His-30 and the evolutionary conservation of product inhibition. These data also provide more direct intracellular evidence for the signaling role associated with H 2O2.

Original languageEnglish
Pages (from-to)12769-12776
Number of pages8
JournalJournal of Biological Chemistry
Volume279
Issue number13
DOIs
StatePublished - Mar 26 2004

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