陶氏病
τ蛋白
高磷酸化
神经科学
Tau病理学
生物
计算生物学
疾病
化学
细胞生物学
阿尔茨海默病
神经退行性变
病理
医学
激酶
作者
Geoffrey Canet,Emma Rocaboy,Sofia Diego-Diàz,Robert A. Whittington,Carl Julien,Emmanuel Planel
出处
期刊:Methods in molecular biology
日期:2024-01-01
卷期号:: 323-341
标识
DOI:10.1007/978-1-0716-3629-9_17
摘要
The intracellular accumulation of microtubule-associated protein tau is a characteristic feature of tauopathies, a group of neurodegenerative diseases including Alzheimer's disease. Formation of insoluble tau aggregates is initiated by the abnormal hyperphosphorylation and oligomerization of tau. Over the past decades, multiple transgenicTransgenetransgenic rodent models mimicking tauopathies have been develop, showcasing this neuropathological hallmark. The biochemical analysis of insoluble tau in these models has served as a valuable tool to understand the progression of tau-related pathology. In this chapter, we provide a comprehensive review of the two primary methods for isolating insoluble tau, namely, sarkosyl and formic acid extraction (and their variants), which are employed for biochemical analysis in transgenicTransgenetransgenic mouse models of tauopathy. We also analyze the strengths and limitations of these methods.
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