The intrinsic amyloidogenic propensity of cofilin-1 is aggravated by Cys-80 oxidation: A possible link with neurodegenerative diseases

Biochem Biophys Res Commun. 2021 Sep 10:569:187-192. doi: 10.1016/j.bbrc.2021.07.013. Epub 2021 Jul 10.

Abstract

Cofilin-1, an actin dynamizing protein, forms actin-cofilin rods, which is one of the major events that exacerbates the pathophysiology of amyloidogenic diseases. Cysteine oxidation in cofilin-1 under oxidative stress plays a crucial role in the formation of these rods. Others and we have reported that cofilin-1 possesses a self-oligomerization property in vitro and in vivo under physiological conditions. However, it remains elusive if cofilin-1 itself forms amyloid-like structures. We, therefore, hypothesized that cofilin-1 might form amyloid-like assemblies, with a potential to intensify the pathophysiology of amyloid-linked diseases. We used various in silico and in vitro techniques and examined the amyloid-forming propensity of cofilin-1. The study confirms that cofilin-1 possesses an intrinsic tendency of aggregation and forms amyloid-like structures in vitro. Further, we studied the effect of cysteine oxidation on the stability and structural features of cofilin-1. Our data show that oxidation at Cys-80 renders cofilin-1 unstable, leading to a partial loss of protein structure. The results substantiate our hypothesis and establish a strong possibility that cofilin-1 aggregation might play a role in cofilin-mediated pathology and the progression of several amyloid-linked diseases.

Keywords: Actin dynamics; Actin-cofilin rods; Alzheimer's disease; Amyloids; Cofilin-1; Oxidative stress.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alzheimer Disease / diagnosis
  • Alzheimer Disease / genetics
  • Alzheimer Disease / metabolism
  • Amino Acid Sequence
  • Amyloid / chemistry
  • Amyloid / metabolism
  • Amyloidogenic Proteins / chemistry
  • Amyloidogenic Proteins / genetics
  • Amyloidogenic Proteins / metabolism*
  • Cofilin 1 / chemistry
  • Cofilin 1 / genetics
  • Cofilin 1 / metabolism*
  • Computer Simulation
  • Cysteine / chemistry
  • Cysteine / genetics
  • Cysteine / metabolism*
  • Humans
  • Models, Molecular
  • Mutation
  • Neurodegenerative Diseases / diagnosis
  • Neurodegenerative Diseases / genetics
  • Neurodegenerative Diseases / metabolism*
  • Oxidation-Reduction
  • Propensity Score
  • Protein Aggregation, Pathological / genetics
  • Protein Aggregation, Pathological / metabolism
  • Protein Stability
  • Protein Unfolding
  • Sequence Homology, Amino Acid

Substances

  • Amyloid
  • Amyloidogenic Proteins
  • Cofilin 1
  • Cysteine