Centre for Misfolding Diseases, Department of Chemistry , University of Cambridge , Lensfield Road , Cambridge CB2 1EW , U.K.
Department of Biology and Biological Engineering, Division of Chemical Biology , Chalmers University of Technology , Kemivägen 10 , 412 96 Gothenburg , Sweden.
Biochemistry. 2019 Oct 1;58(39):4086-4095. doi: 10.1021/acs.biochem.9b00592. Epub 2019 Sep 18.
TAR DNA-binding protein 43 (TDP-43) has been identified as the major constituent of the proteinaceous inclusions that are characteristic of most forms of amyotrophic lateral sclerosis (ALS) and ubiquitin positive frontotemporal lobar degeneration (FTLD). Wild type TDP-43 inclusions are a pathological hallmark of >95% of patients with sporadic ALS and of the majority of familial ALS cases, and they are also found in a significant proportion of FTLD cases. ALS is the most common form of motor neuron disease, characterized by progressive weakness and muscular wasting, and typically leads to death within a few years of diagnosis. To determine how the translocation and misfolding of TDP-43 contribute to ALS pathogenicity, it is crucial to define the dynamic behavior of this protein within the cellular environment. It is therefore necessary to develop cell models that allow the location of the protein to be defined. We report the use of TDP-43 with a tetracysteine tag for visualization using fluorogenic biarsenical compounds and show that this model displays features of ALS observed in other cell models. We also demonstrate that this labeling procedure enables live-cell imaging of the translocation of the protein from the nucleus into the cytosol.
TAR DNA 结合蛋白 43(TDP-43)已被确定为大多数肌萎缩侧索硬化症(ALS)和泛素阳性额颞叶变性(FTLD)的蛋白包涵体的主要成分。野生型 TDP-43 包涵体是 >95%散发性 ALS 患者和大多数家族性 ALS 病例的病理学标志,并且在相当一部分 FTLD 病例中也发现了它们。ALS 是最常见的运动神经元疾病形式,其特征是进行性无力和肌肉萎缩,通常在诊断后的几年内导致死亡。为了确定 TDP-43 的易位和错误折叠如何导致 ALS 的致病性,确定该蛋白在细胞环境中的动态行为至关重要。因此,有必要开发允许定义蛋白质位置的细胞模型。我们报告了使用带有四半胱氨酸标签的 TDP-43 来使用荧光生物砷化合物进行可视化,并表明该模型显示了其他细胞模型中观察到的 ALS 特征。我们还证明,这种标记程序能够对蛋白质从核到细胞质的易位进行活细胞成像。