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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.
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页码:8558 / 8565
页数:8
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