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在tau蛋白病转基因小鼠模型中对不溶性tau蛋白进行生化分离。

Biochemical isolation of insoluble tau in transgenic mouse models of tauopathies.

作者信息

Julien Carl, Bretteville Alexis, Planel Emmanuel

机构信息

Axe Neurosciences, Centre Hospitalier de l'Université Laval, Québec, QC, Canada.

出版信息

Methods Mol Biol. 2012;849:473-91. doi: 10.1007/978-1-61779-551-0_32.

Abstract

Tau is a highly soluble microtubule-associated protein (MAP) that is abundant in the central nervous system and expressed mainly in neuronal axons. Intracellular aggregates of insoluble tau protein are present in a group of neurodegenerative diseases called tauopathies, which include Alzheimer's disease. Numerous transgenic mouse models of tauopathies have been produced in the last decade, and analysis of insoluble tau in these animals has provided a powerful tool to understand the development of tau pathology. In this short chapter, we aim at reviewing the two main isolation methods, sarkosyl and formic acid extraction (and their variations), used for the biochemical isolation of insoluble tau in transgenic mouse models of tauopathy, and discuss their advantages and drawbacks.

摘要

Tau是一种高度可溶的微管相关蛋白(MAP),在中枢神经系统中含量丰富,主要在神经元轴突中表达。不溶性tau蛋白的细胞内聚集体存在于一组称为tau蛋白病的神经退行性疾病中,其中包括阿尔茨海默病。在过去十年中已经产生了许多tau蛋白病的转基因小鼠模型,对这些动物中不溶性tau的分析为理解tau病理学的发展提供了一个强大的工具。在这一简短章节中,我们旨在综述用于tau蛋白病转基因小鼠模型中不溶性tau生化分离的两种主要分离方法,即十二烷基肌氨酸钠和甲酸提取法(及其变体),并讨论它们的优缺点。

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