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Dual Functional Small Molecule Probes as Fluorophore and Ligand for Misfolding Proteins

机译:双功能小分子探针作为荧光团和配体用于错误折叠蛋白质

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摘要

Misfolding of a protein is a destructive process for variety of diseases that include neurodegenerative diseases such as Alzheimer’s disease, Parkinson disease, Huntington disease, mad cow disease, amyotrophic lateral sclerosis (ALS), and frontal temporal dementia (FTD), and other non-CNS diseases such as diabetes, cystic fibrosis, and lysosomal storage diseases. Formation of various misfunctional large assembles of the misfolded protein is the primary consequence. To detect the formation of the aggregated species is very important for not only basic mechanism research but also very crucial for diagnosis of the diseases. In this review, we updated references related to the new development of the dual functional fluorescent small molecule probes for detecting the aggregated proteins in vitro and in vivo.
机译:蛋白质错误折叠是多种疾病的破坏性过程,包括神经退行性疾病,例如阿尔茨海默氏病,帕金森氏病,亨廷顿病,疯牛病,肌萎缩性侧索硬化症(ALS)和额颞痴呆(FTD),以及其他非中枢神经系统疾病,例如糖尿病,囊性纤维化和溶酶体贮积病。形成错误折叠的蛋白质的各种功能失常的大组装体是主要的结果。检测聚集物种的形成不仅对于基础机理研究非常重要,而且对于疾病的诊断也非常重要。在这篇综述中,我们更新了与用于检测体内和体外聚集蛋白的双功能荧光小分子探针新进展相关的参考文献。

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