monomerization of Cu, Zn superoxide
dismutase (SOD1) is an early step along pathways of
misfolding linked to amyotrophic lateral sclerosis (ALS).
Monomerization requires the reversal of two post-translational
modifications that are thermodynamically favorable: (i)
dissociation of active-site metal ions and (ii) reduction of
intramolecular disulfide bonds. This study found, using amide
hydrogen/deuterium (H/D) exchange, capillary electrophoresis,
and lysine-acetyl protein charge ladders, that ALS-linked A4V SOD1 rapidly monomerizes and partially unfolds in an
external electric field (of physiological strength), without loss of metal ions, exposure to disulfide-reducing agents, or Joule
heating. Voltage-induced monomerization was not observed for metal-free A4V SOD1, metal-free WT SOD1, or metal-loaded
WT SOD1. Computational modeling suggested a mechanism for this counterintuitive effect: subunit macrodipoles of dimeric
SOD1 are antiparallel and amplified 2-fold by metal coordination, which increases torque at the dimer interface as subunits rotate
to align with the electric field.