Yusuf Hamied Department of Chemistry, University of Cambridge, Cambridge, United Kingdom; UK Dementia Research Institute, Department of Clinical Neurosciences, University of Cambridge, Cambridge, United Kingdom.
Neurobiol Dis. 2021 Jun;153:105327. doi: 10.1016/j.nbd.2021.105327. Epub 2021 Mar 9.
The aggregation of misfolded proteins is a fundamental pathology in neurodegeneration which remains poorly understood due to its exceptional complexity and lack of appropriate characterization tools that can probe the role of the low concentrations of heterogeneous protein aggregates formed during the progression of the disease. In this review, we explain the principles underlying the operation of single molecule microscopy, an imaging method that can resolve molecules one-by-one, its application to imaging and characterizing individual protein aggregates in human samples and in vitro as well as the important questions in neurobiology this has answered and can answer.
蛋白质错误折叠的聚集是神经退行性变的一种基本病理学现象,但由于其异常复杂性和缺乏适当的特征化工具,使得人们对其仍然了解甚少,这些工具可以探测在疾病进展过程中形成的低浓度异质蛋白质聚集体的作用。在这篇综述中,我们解释了单分子显微镜操作的原理,这是一种可以逐个分辨分子的成像方法,以及它在人类样本和体外成像和特征化单个蛋白质聚集体中的应用,以及它已经回答和可以回答的神经生物学中的重要问题。