Inhibition of Beta-Arrestin 1 and Beta-Arrestin2 Oligomerlzation in Taupathy

Tech ID: 19B170

Competitive Advantages

  • Small molecule inhibitors that target beta-arrestin oligomerization and accumulation of pathogenic tau
  • Novel treatment for tauopathies
  • Could be a therapeutic for numerous neurodegenerative disorders

Summary

Tau pathology (tauopathy) is a prevailing hallmark of multiple neurodegenerative disease, including Alzheimer’s disease and frontotemporal lobar degeneration (FTLD). Our researchers have shown that beta-arrestin is increased in FTLD and plays a significant role in promoting tauopathy in brain. They discovered that β-arrestin oligomers, not monomers, promote tau accumulation and aggregation, and loss of beta-arrestin oligomers reduces pathogenic tau accumulation in brain.

Our researchers screened and identified novel inhibitors that beta-arrestin oligomerization and accumulation of tau in cells. This is a novel and promising therapeutic approach to mitigate tauopathies and related neurodegenerative diseases.

β-arrestin2 inhibitor compounds C1 and C2 reduce tau levels in HeLa-V5 tau cells (Western Blot Analysis; 10uM treatment for 6 hrs).
 

Desired Partnerships

  • License
  • Sponsored Research
  • Co-Development

 

 

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