Engineering and characterization of human manganese superoxide dismutase mutants with high activity and low product inhibition

Karuppiah Chockalingam, James Luba, Harry S. Nick, David N. Silverman, Huimin Zhao

Research output: Contribution to journalArticlepeer-review

Abstract

Human manganese superoxide dismutase is a mitochondrial metalloenzyme that is involved in protecting aerobic organisms against superoxide toxicity, and has been implicated in slowing tumor growth. Unfortunately, this enzyme exhibits strong product inhibition, which limits its potential biomedical applications. Previous efforts to alleviate human manganese superoxide dismutase product inhibition utilized rational protein design and site-directed mutagenesis. These efforts led to variants of human manganese superoxide dismutase at residue 143 with dramatically reduced product inhibition, but also reduced catalytic activity and efficiency. Here, we report the use of a directed evolution approach to engineer two variants of the Q143A human manganese superoxide dismutase mutant enzyme with improved catalytic activity and efficiency. Two separate activity-restoring mutations were found - C140S and N73S - that increase the catalytic efficiency of the parent Q143A human manganese superoxide dismutase enzyme by up to five-fold while maintaining low product inhibition. Interestingly, C140S is a context-dependent mutation, and the C140S-Q143A human manganese superoxide dismutase did not follow Michaelis-Menten kinetics. The re-engineered human manganese superoxide dismutase mutants should be useful for biomedical applications, and our kinetic and structural studies also provide new insights into the structure-function relationships of human manganese superoxide dismutase.

Original languageEnglish (US)
Pages (from-to)4853-4861
Number of pages9
JournalFEBS Journal
Volume273
Issue number21
DOIs
StatePublished - Nov 2006

Keywords

  • Directed evolution
  • Gene therapy
  • Kinetic analysis
  • Product inhibition

ASJC Scopus subject areas

  • Biochemistry

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