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Phosphorylated tau targeted small-molecule PROTACs for the treatment of Alzheimer's disease and tauopathies

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ELSEVIER
DOI: 10.1016/j.bbadis.2021.166162

关键词

Alzheimer's disease; Tau protein; Hyperphosphorylation; Neurofibrillary tangles; Paired helical filament; PROTACs; Tauopathies

资金

  1. NIH [R01AG042178, R01AG47812, R01NS105473, AG060767, AG069333, AG066347]

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Tau protein is essential for the formation of axonal microtubules in neurons. Phosphorylated tau (p-Tau) is being explored as a therapeutic target for Alzheimer's disease (AD) due to its association with synaptic damage and neuronal dysfunction. Alternative therapeutic strategies like p-tau-PROTACs targeted small molecules are being considered in light of continuous failures in Aβ-targeted clinical trials.
Tau is a microtubule-stabilizing protein that plays an important role in the formation of axonal microtubules in neurons. Phosphorylated tau (p-Tau) has received great attention in the field of Alzheimer's disease (AD) as a potential therapeutic target due to its involvement with synaptic damage and neuronal dysfunction. Mounting evidence suggests that amyloid beta (A beta)-targeted clinical trials continuously failed; therefore, it is important to consider alternative therapeutic strategies such as p-tau-PROTACs targeted small molecules for AD and other tauopathies. The present article describes the characteristics of tau biology, structure, and function in both healthy and pathological states in AD. It also explains data from studies that have identified the involvement of ptau in neuronal damage and synaptic and cognitive functions in AD. Current article also covers several aspects, including small molecule inhibitors, and the development of p-tau-PROTACs targeted drug molecules to treat patients with AD and other tauopathies.

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