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Updated: Sep 22, 2025

Nuclear Magnetic Resonance Spectroscopy for the Identification of Multiple Phosphorylations of Intrinsically Disordered Proteins
Published on: December 27, 2016
Dephosphorylation Targeting Chimaera (DEPTAC): Targeting Tau Proteins in Tauopathies
Andrea Soumbasis1, Mohamed A Eldeeb1, Mohamed A Ragheb2
1Department of Neurology and Neurosurgery, Neurodegenerative Diseases Group, McGill Parkinson Program, Montreal Neurological Institute, McGill University, Montreal, Quebec, Canada.
Abstract:
One salient hallmark of neurodegeneration is the accumulation of toxic protein aggregates in neuronal cells. This proteotoxicity culminates in the deterioration of neuronal function. In AD and related tauopathies, the microtubule-associated protein tau becomes hyperphosphorylated. Hyperphosphorylated tau forms neurofibrillary tangles (NFTs) within neurons, which constitute a unique feature of tauopathies, including AD. A recent study has exploited a novel molecular strategy to counteract hyperphosphorylated tau and enhance its degradation. Analogous to the PROTAC methodology, a novel dephosphorylation targeting chimera (DEPTAC) was designed to promote the molecular interaction between tau and phosphatase, which, in turn, augments its degradation. Herein, we briefly discuss this novel finding and its potential therapeutic implications.
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