硫黄素
化学
荧光
自体荧光
量子点
生物物理学
淀粉样蛋白(真菌学)
纳米技术
阿尔茨海默病
疾病
光学
病理
医学
无机化学
物理
材料科学
生物
作者
Li Na Quan,Jiangxiao Wu,Lucas A. Lane,Jianquan Wang,Qian Lu,Zheng Gu,Yiqing Wang
标识
DOI:10.1021/acs.bioconjchem.6b00019
摘要
Diagnostics of Alzheimer's disease (AD) commonly employ the use of fluorescent thioflavin derivatives having affinity for the amyloid-β (Aβ) proteins associated with AD progression. However, thioflavin probes have limitations in their diagnostic capabilities arising from a number of undesireable qualities, including poor photostability, weak emission intensity, and high emission overlap with the backgound tissue autofluorescence. To overcome such limitations, we have developed nanoformulated probes consisting of a red-emitting fluorescent quantum dot (QD) core encapsulated in a PEGylated shell with benzotriazole (BTA) targeting molecules on the surface (QD-PEG-BTA). The combination of strong red fluorescence, multivalent binding, and decreased backgound signal and nonspecific binding provided the ability of the QD-PEG-BTA probes to achieve detection sensitivites 4 orders of magnitude greater than those of conventional thioflavin derivatives. This study opens the door for the use of QDs in AD detection applications.
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