神经退行性变
脱磷
τ蛋白
磷酸化
神经科学
细胞生物学
陶氏病
嵌合体(遗传学)
化学
生物
磷酸酶
生物化学
阿尔茨海默病
医学
病理
疾病
基因
作者
Andrea Soumbasis,Mohamed A. Eldeeb,Mohamed A. Ragheb,Cornelia E. Zorca
出处
期刊:Current Protein & Peptide Science
[Bentham Science Publishers]
日期:2022-03-01
卷期号:23 (3): 129-132
被引量:1
标识
DOI:10.2174/1389203723666220519154229
摘要
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI