硫黄素
透射电子显微镜
蛋白质丝
显微镜
化学
τ蛋白
生物物理学
纳米
荧光
蛋白质聚集
电子显微镜
发病机制
纳米技术
材料科学
物理
生物
光学
疾病
阿尔茨海默病
生物化学
医学
病理
免疫学
作者
Carol J. Huseby,Jeff Kuret
出处
期刊:Methods in molecular biology
日期:2016-01-01
卷期号:: 101-112
被引量:11
标识
DOI:10.1007/978-1-4939-2978-8_7
摘要
Conversion of monomeric tau protein into filamentous aggregates is a defining event in the pathogenesis of Alzheimer’s disease. To gain insight into disease pathogenesis, the mechanisms that trigger and mediate tau aggregation are under intense investigation. Characterization efforts have relied primarily on recombinant tau protein preparations and high-throughput solution-based detection methods such as thioflavin-dye fluorescence and laser-light-scattering spectroscopies. Transmission electron microscopy (TEM) is a static imaging tool that complements these approaches by detecting individual tau filaments at nanometer resolution. In doing so, it can provide unique insight into the quality, quantity, and composition of synthetic tau filament populations. Here we describe protocols for analysis of tau filament populations by TEM for purposes of dissecting aggregation mechanism.
科研通智能强力驱动
Strongly Powered by AbleSci AI