Detection and characterization of TDP-43 in human cells and tissues by multiple reaction monitoring mass spectrometry

Pub Date : 2019-11-01 Epub Date: 2019-07-19 DOI:10.1016/j.clinms.2019.07.003
Taylor D. Pobran , Lauren M. Forgrave , Yu Zi Zheng , John G.K. Lim , Ian R.A. Mackenzie , Mari L. DeMarco
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引用次数: 5

Abstract

Transactive response DNA-binding protein 43 kDa (TDP-43) is a highly conserved and widely expressed protein in human tissues that regulates nucleic acid processing. In frontotemporal dementia and amyotrophic lateral sclerosis, however, TDP-43 forms insoluble aggregates in central nervous tissues. These pathological deposits of TDP-43 have been primarily studied by ligand binding, namely western blot analysis, and, thus, methods with greater structural resolution are needed to aid in our understanding of the pathological processes associated with TDP-43 misfolding and aggregation. Toward this goal, we have developed a selective and multiplex method for the detection and characterization of TDP-43 using liquid chromatography tandem mass spectrometry. As proof-of-concept, the method was applied to the detection and characterization of TDP-43 in human cell lines and human brain tissue.

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多反应监测质谱法检测和表征人细胞和组织中的TDP-43
dna结合蛋白43 kDa (TDP-43)是一种在人体组织中高度保守且广泛表达的调节核酸加工的蛋白。然而,在额颞叶痴呆和肌萎缩侧索硬化症中,TDP-43在中枢神经组织中形成不溶性聚集体。这些TDP-43的病理沉积主要是通过配体结合,即western blot分析来研究的,因此,需要更高结构分辨率的方法来帮助我们理解与TDP-43错误折叠和聚集相关的病理过程。为了实现这一目标,我们开发了一种选择性和多重方法,用于使用液相色谱串联质谱法检测和表征TDP-43。作为概念验证,该方法被应用于人类细胞系和人脑组织中TDP-43的检测和表征。
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