Misfolded mutant SOD1 directly inhibits VDAC1 conductance in a mouse model of inherited ALS

Adrian Israelson, Nir Arbel, Sandrine Da Cruz, Hristelina Ilieva, Koji Yamanaka, Varda Shoshan-Barmatz, Don W. Cleveland

Research output: Contribution to journalArticlepeer-review

Abstract

Mutations in superoxide dismutase (SOD1) cause amyotrophic lateral sclerosis (ALS), a neurodegenerative disease characterized by loss of motor neurons. With conformation-specific antibodies, we now demonstrate that misfolded mutant SOD1 binds directly to the voltage-dependent anion channel (VDAC1), an integral membrane protein imbedded in the outer mitochondrial membrane. This interaction is found on isolated spinal cord mitochondria and can be reconstituted with purified components in vitro. ADP passage through the outer membrane is diminished in spinal mitochondria from mutant SOD1-expressing ALS rats. Direct binding of mutant SOD1 to VDAC1 inhibits conductance of individual channels when reconstituted in a lipid bilayer. Reduction of VDAC1 activity with targeted gene disruption is shown to diminish survival by accelerating onset of fatal paralysis in mice expressing the ALS-causing mutation SOD1G37R. Taken together, our results establish a direct link between misfolded mutant SOD1 and mitochondrial dysfunction in this form of inherited ALS.

Original languageEnglish (US)
Pages (from-to)575-587
Number of pages13
JournalNeuron
Volume67
Issue number4
DOIs
StatePublished - Aug 2010

Keywords

  • Cellbio
  • Humdisease
  • Molneuro

ASJC Scopus subject areas

  • Neuroscience(all)

Fingerprint Dive into the research topics of 'Misfolded mutant SOD1 directly inhibits VDAC1 conductance in a mouse model of inherited ALS'. Together they form a unique fingerprint.

Cite this