SARS-CoV-2 spike protein interactions with amyloidogenic proteins: Potential clues to neurodegeneration

Biochem Biophys Res Commun. 2021 May 21:554:94-98. doi: 10.1016/j.bbrc.2021.03.100. Epub 2021 Mar 24.

Abstract

The post-infection of COVID-19 includes a myriad of neurologic symptoms including neurodegeneration. Protein aggregation in brain can be considered as one of the important reasons behind the neurodegeneration. SARS-CoV-2 Spike S1 protein receptor binding domain (SARS-CoV-2 S1 RBD) binds to heparin and heparin binding proteins. Moreover, heparin binding accelerates the aggregation of the pathological amyloid proteins present in the brain. In this paper, we have shown that the SARS-CoV-2 S1 RBD binds to a number of aggregation-prone, heparin binding proteins including Aβ, α-synuclein, tau, prion, and TDP-43 RRM. These interactions suggests that the heparin-binding site on the S1 protein might assist the binding of amyloid proteins to the viral surface and thus could initiate aggregation of these proteins and finally leads to neurodegeneration in brain. The results will help us to prevent future outcomes of neurodegeneration by targeting this binding and aggregation process.

Keywords: COVID-19; Heparin; Heparin binding proteins; Neurodegeneration; Protein aggregation; SARS-CoV-2.

MeSH terms

  • Amyloid / metabolism*
  • Amyloid beta-Peptides / metabolism
  • Brain / metabolism
  • Brain / pathology
  • Brain / virology
  • COVID-19 / metabolism*
  • COVID-19 / virology
  • DNA-Binding Proteins / chemistry
  • DNA-Binding Proteins / metabolism
  • Heparin / metabolism*
  • Humans
  • Molecular Docking Simulation
  • Neurodegenerative Diseases / metabolism*
  • Neurodegenerative Diseases / virology
  • Prions / metabolism
  • Protein Aggregation, Pathological*
  • Protein Binding
  • SARS-CoV-2 / chemistry
  • SARS-CoV-2 / metabolism
  • SARS-CoV-2 / pathogenicity*
  • Spike Glycoprotein, Coronavirus / chemistry
  • Spike Glycoprotein, Coronavirus / metabolism*
  • alpha-Synuclein / metabolism
  • tau Proteins / metabolism

Substances

  • Amyloid
  • Amyloid beta-Peptides
  • DNA-Binding Proteins
  • Prions
  • Spike Glycoprotein, Coronavirus
  • TARDBP protein, human
  • alpha-Synuclein
  • spike protein, SARS-CoV-2
  • tau Proteins
  • Heparin