τ蛋白
化学
微管
负染色法
生物物理学
聚合
体外
重组DNA
生物化学
电子显微镜
阿尔茨海默病
细胞生物学
生物
病理
疾病
医学
聚合物
有机化学
物理
基因
光学
作者
Stefan Barghorn,Jacek Biernat,Eckhard Mandelkow�
出处
期刊:Humana Press eBooks
[Humana Press]
日期:2005-06-24
卷期号:: 035-052
被引量:198
标识
DOI:10.1385/1-59259-874-9:035
摘要
The tau protein is a neuronal microtubule-associated protein. Apart of its physiological function/3-the binding to and stabilization of microtubules/3-tau is found in Alzheimer's disease brain as insoluble fibers, the so-called "paired helical filaments" (PHFs). Investigating the fundamentals of tau polymerization is indispensable for identifying inhibitory conditions or compounds preventing PHF formation, which may slow down or even stop the degeneration of neurons in Alzheimer's disease. In this chapter, we describe the methods necessary for studying the characteristics of tau polymerization to PHFs. These include: a purification protocol for recombinantly expressed tau; a general method for the polyanion induced polymerization of tau to PHFs; the quantitation of PHFs by a fluorescence-based assay; the imaging and verification of PHFs by negative stain transmission electron microscopy.
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