Zhang Xueli, Ran Chongzhao
Molecular Imaging Laboratory, MGH/MIT/HMS Athinoula A. Martinos Center for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital/Harvard Medical School, Room 2301, Building 149, Charlestown, Boston, Massachusetts 02129 ; Center for Drug Discovery, School of Pharmacy, China Pharmaceutical University, Nanjing, China.
Molecular Imaging Laboratory, MGH/MIT/HMS Athinoula A. Martinos Center for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital/Harvard Medical School, Room 2301, Building 149, Charlestown, Boston, Massachusetts 02129.
Curr Org Chem. 2013 Mar 1;17(6). doi: 10.2174/1385272811317060004.
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 and .
蛋白质错误折叠是多种疾病的破坏性过程,这些疾病包括神经退行性疾病,如阿尔茨海默病、帕金森病、亨廷顿病、疯牛病、肌萎缩侧索硬化症(ALS)和额颞叶痴呆(FTD),以及其他非中枢神经系统疾病,如糖尿病、囊性纤维化和溶酶体贮积病。错误折叠蛋白质形成各种功能异常的大聚集体是主要后果。检测聚集物种的形成不仅对基础机制研究非常重要,而且对疾病诊断也至关重要。在本综述中,我们更新了与用于检测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。