Dephosphorylation Targeting Chimaera (DEPTAC): Targeting Tau Proteins in Tauopathies

Author:

Soumbasis Andrea1,Eldeeb Mohamed A.1,Ragheb Mohamed A.2,Zorca Cornelia E.1

Affiliation:

1. Department of Neurology and Neurosurgery, Neurodegenerative Diseases Group, McGill Parkinson Program, Montreal Neurological Institute, McGill University, Montreal, Quebec, Canada

2. Department of Chemistry, Faculty of Science, Cairo University, Giza, Cairo, Egypt

Abstract

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.

Publisher

Bentham Science Publishers Ltd.

Subject

Cell Biology,Molecular Biology,Biochemistry,General Medicine

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Targeted protein degradation: from mechanisms to clinic;Nature Reviews Molecular Cell Biology;2024-04-29

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