化学
硫黄素
高通量筛选
淀粉样蛋白(真菌学)
肽
荧光
小分子
阿尔茨海默病
筛选技术
蛋白质聚集
体外
淀粉样前体蛋白
生物化学
疾病
生物信息学
病理
物理
无机化学
生物
医学
量子力学
作者
Kairit Zovo,Eneken Helk,Ann Karafin,Vello Tõugu,Peep Palumaa
摘要
Aggregation of amyloid-β (Aβ) peptides is causatively linked to Alzheimer's disease (AD); thus, suppression of this process by small molecule inhibitors is a widely accepted therapeutic and preventive strategy for AD. Screening of the inhibitors of Aβ aggregation deserves much attention; however, despite intensive efforts, there are only a few high-throughput screening methods available, all of them having drawbacks related to the application of external fluorescent probes or artificial Aβ derivatives. We have developed a label-free MALDI MS-based screening test for inhibitors of Aβ₄₂ fibrillization that exhibits high sensitivity, speed, and automation possibilities suitable for high-throughput screening. The test was evaluated by transmission electron microscopy and compared with a fluorimetric thioflavin-based assay, where interference of a number of tested compounds with thioflavin T binding and/or fluorescence caused false-positive results. The MALDI MS-based method can significantly speed up in vitro screening of compound libraries for inhibitors of Aβ₄₂ fibrillization.
科研通智能强力驱动
Strongly Powered by AbleSci AI