菁
硫黄素
淀粉样蛋白(真菌学)
纤维
化学
荧光
体外
生物物理学
淀粉样纤维
胰岛素
生物化学
淀粉样β
生物
阿尔茨海默病
医学
无机化学
物理
疾病
量子力学
内分泌学
病理
作者
KD Volkova,Vladyslava Kovalska,D Inshin,Yu. L. Slominskiĭ,OI Tolmachev,S. M. Yarmoluk
标识
DOI:10.3109/10520291003648466
摘要
Fluorescence spectroscopy was used to study the ability of dye 7519 to follow the transition of monomeric insulin into fibrils and applicability of the dye to the insulin aggregation inhibition assay. The commercially available classic amyloid stain, thioflavin T, was used as the reference dye. For selecting potential inhibitors, the QSAR approach was applied. Dye 7519 appeared to be suitable for monitoring insulin aggregation into fibrils in vitro. The properties of the dye allowed us to test it as a potential probe in the screening assay of potential inhibitors of insulin fibrillization. One hundred forty-four flavonoids were tested as potential inhibitors of amyloid fibril formation using the quantitative structure activity relationship approach. Among them, 10 candidates with high indexes of inhibition were selected for tests in vitro using dye 7519 and the reference amyloid dye thioflavine T. Using dye 7519 fluorescence, we found that two compounds had inhibitory effects on insulin amyloid formation. These results agree with inhibition data using the thioflavine T assay. Our studies demonstrated that the fluorescent cyanine dye 7519 is a sensitive probe for quantitative detection of insulin amyloid formation and can be applied to screen agents capable of affecting aggregation of amyloid proteins.
科研通智能强力驱动
Strongly Powered by AbleSci AI