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Research Article

Strategies for stabilizing superoxide dismutase (SOD1), the protein destabilized in the most common form of familial amyotrophic lateral sclerosis

Jared R. Auclair, Kristin J. Boggio, Gregory A. Petsko, Dagmar Ringe, and Jeffrey N. Agar
PNAS first published November 22, 2010; https://doi.org/10.1073/pnas.1015463107
Jared R. Auclair
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Kristin J. Boggio
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Gregory A. Petsko
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Dagmar Ringe
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Jeffrey N. Agar
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  • For correspondence: agar@brandeis.edu
  1. Contributed by Gregory A. Petsko, October 18, 2010 (sent for review November 1, 2009)

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Abstract

Amyotrophic lateral sclerosis (ALS) is a disorder characterized by the death of both upper and lower motor neurons and by 3- to 5-yr median survival postdiagnosis. The only US Food and Drug Administration-approved drug for the treatment of ALS, Riluzole, has at best, moderate effect on patient survival and quality of life; therefore innovative approaches are needed to combat neurodegenerative disease. Some familial forms of ALS (fALS) have been linked to mutations in the Cu/Zn superoxide dismutase (SOD1). The dominant inheritance of mutant SOD1 and lack of symptoms in knockout mice suggest a “gain of toxic function” as opposed to a loss of function. A prevailing hypothesis for the mechanism of the toxicity of fALS-SOD1 variants, or the gain of toxic function, involves dimer destabilization and dissociation as an early step in SOD1 aggregation. Therefore, stabilizing the SOD1 dimer, thus preventing aggregation, is a potential therapeutic strategy. Here, we report a strategy in which we chemically cross-link the SOD1 dimer using two adjacent cysteine residues on each respective monomer (Cys111). Stabilization, measured as an increase in melting temperature, of ∼20 °C and ∼45 °C was observed for two mutants, G93A and G85R, respectively. This stabilization is the largest for SOD1, and to the best of our knowledge, for any disease-related protein. In addition, chemical cross-linking conferred activity upon G85R, an otherwise inactive mutant. These results demonstrate that targeting these cysteine residues is an important new strategy for development of ALS therapies.

  • mass spectrometry
  • thiol-disulfide

Footnotes

  • 1To whom correspondence should be addressed. E-mail: agar{at}brandeis.edu.
  • Author contributions: J.R.A., G.A.P., D.R., and J.N.A. designed research; J.R.A. and K.J.B. performed research; J.R.A., G.A.P., D.R., and J.N.A. analyzed data; and J.R.A., G.A.P., D.R., and J.N.A. wrote the paper.

  • Conflict of interest statement: A patent has been filed by the authors relating to the strategy of SOD1 stabilization described here.

  • This article contains supporting information online at www.pnas.org/lookup/suppl/doi:10.1073/pnas.1015463107/-/DCSupplemental.

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Strategies for stabilizing superoxide dismutase (SOD1), the protein destabilized in the most common form of familial amyotrophic lateral sclerosis
Jared R. Auclair, Kristin J. Boggio, Gregory A. Petsko, Dagmar Ringe, Jeffrey N. Agar
Proceedings of the National Academy of Sciences Nov 2010, DOI: 10.1073/pnas.1015463107

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Strategies for stabilizing superoxide dismutase (SOD1), the protein destabilized in the most common form of familial amyotrophic lateral sclerosis
Jared R. Auclair, Kristin J. Boggio, Gregory A. Petsko, Dagmar Ringe, Jeffrey N. Agar
Proceedings of the National Academy of Sciences Nov 2010, DOI: 10.1073/pnas.1015463107
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