硫黄素
肽
荧光
化学
表面改性
淀粉样蛋白(真菌学)
生物物理学
生物化学
阿尔茨海默病
纳米技术
细胞生物学
生物
材料科学
疾病
医学
病理
物理
物理化学
无机化学
量子力学
作者
Francisco Morales-Zavala,Nathalie Casanova‐Morales,Raúl B. Gonzalez,América Chandía-Cristi,Lisbell D. Estrada,I. Alvizu,Victor Waselowski,Fanny Guzmàn,Simón Guerrero,Marisol Oyarzún-Olave,C. Rebolledo Espinoza,Enrique Rodríguez,Julien Armijo,H. Bhuyan,M. Favre,Alejandra Álvarez,Marcelo J. Kogan,J. R. Maze
标识
DOI:10.1186/s12951-018-0385-7
摘要
Stable and non-toxic fluorescent markers are gaining attention in molecular diagnostics as powerful tools for enabling long and reliable biological studies. Such markers should not only have a long half-life under several assay conditions showing no photo bleaching or blinking but also, they must allow for their conjugation or functionalization as a crucial step for numerous applications such as cellular tracking, biomarker detection and drug delivery.We report the functionalization of stable fluorescent markers based on nanodiamonds (NDs) with a bifunctional peptide. This peptide is made of a cell penetrating peptide and a six amino acids long β-sheet breaker peptide that is able to recognize amyloid β (Aβ) aggregates, a biomarker for the Alzheimer disease. Our results indicate that functionalized NDs (fNDs) are not cytotoxic and can be internalized by the cells. The fNDs allow ultrasensitive detection (at picomolar concentrations of NDs) of in vitro amyloid fibrils and amyloid aggregates in AD mice brains.The fluorescence of functionalized NDs is more stable than that of fluorescent markers commonly used to stain Aβ aggregates such as Thioflavin T. These results pave the way for performing ultrasensitive and reliable detection of Aβ aggregates involved in the pathogenesis of the Alzheimer disease.
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