Label-Free High-Throughput Screening Assay for Inhibitors of Alzheimer's Amyloid-β Peptide Aggregation Based on MALDI MS

被引:24
|
作者
Zovo, Kairit [1 ]
Helk, Eneken [1 ]
Karafin, Ann [1 ]
Tougu, Vello [1 ]
Palumaa, Peep [1 ]
机构
[1] Tallinn Univ Technol, Dept Gene Technol, EE-12618 Tallinn, Estonia
关键词
SMALL-MOLECULE INHIBITORS; FIBRILS IN-VITRO; A-BETA; METHYLENE-BLUE; DISEASE; PROTEIN; OLIGOMERIZATION; FIBRILLIZATION; PHENOTHIAZINES; POLYPHENOLS;
D O I
10.1021/ac101583q
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Aggregation of amyloid-beta (A beta) 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 A beta 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 A beta derivatives. We have developed a label-free MALDI MS-based screening test for inhibitors of A beta(42) 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 A beta(42) fibrillization.
引用
收藏
页码:8558 / 8565
页数:8
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