Credit: Gabriel Luna

The focus is on the protein Tau and its misfolding under conditions that lead to neurodegenerative diseases. The focus is on the transition of Tau from a normal microtubule-associated protein to a pathological aggregate. Under study are its intermediate stages during Tau spread and its state as a molecular condensate. The use of intelligently designed peptide binders to prevent Tau aggregation and induce disaggregation are areas of active investigation. Tau co-pathology includes TDP-43 addressed in recently launched projects.

Affiliated Researchers

Principal Investigator
Exploration of fundamental biological processes, particularly those related to the brain and its evolution.
Assistant Project Scientist
Understanding and disrupting the molecular mechanisms underlying tau aggregation and spread in tauopathies.
Project Scientist
Understanding the function of liquid-liquid phase separation (LLPS) of the co-chaperone BAG2 and its relation to tau degradation pathways.
Project Scientist
Studying the transcriptome from single cells in post-mortem brain tissues from Alzheimer’s disease patients.
Postdoctoral Researcher
Investigation of how TDP-43 dysfunction contributes to cellular pathology within the ALS/FTD spectrum.
Postdoctoral Researcher
Studies how the human brain develops and what goes wrong in certain disorders by growing cerebral organoids from stem cells.
Postdoctoral Researcher
Discovery of brain penetrant farnesyltransferase inhibitors for the treatment of tauopathies.
Postdoctoral Researcher
Graduate Student Researcher
Understanding how diseased forms of tau protein spread and drive neurodegeneration.
Laboratory Assistant
Histotechnologist specializing in processing samples for clinical and pathological diagnoses, as well as cellular characterization.

Collaborators

  • Songi Han (Northwestern)
  • Nathan Gianneschi (Northwestern)
  • Yang Yang (Van Andel Institute)
  • Scott Shell (UCSB)
  • Joan Shea (UCSB)