Dye-Binding Assays for Evaluation of the Effects of Small Molecule Inhibitors on Amyloid (Aβ) Self-Assembly

被引:123
作者
Jameson, Laramie P. [1 ]
Smith, Nicholas W. [1 ]
Dzyuba, Sergei V. [1 ]
机构
[1] Texas Christian Univ, Dept Chem, Ft Worth, TX 76129 USA
来源
ACS CHEMICAL NEUROSCIENCE | 2012年 / 3卷 / 11期
关键词
Alzheimer's disease; amyloid peptide; small molecule inhibitor; dye-binding assay; thioflavin T; fluorescence; THIOFLAVIN-T FLUORESCENCE; ALZHEIMERS-DISEASE; CONGO RED; FIBRIL FORMATION; IN-VITRO; SOLUBLE OLIGOMERS; MITOCHONDRIAL DYSFUNCTION; PEPTIDE AGGREGATION; PROTEIN AGGREGATION; SECONDARY STRUCTURE;
D O I
10.1021/cn300076x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Dye-binding assays, such as those utilizing Congo red and thioflavin T, are among the most widely used tools to probe the aggregation of amyloidogenic biomolecules and for the evaluation of small molecule inhibitors of amyloid aggregation and fibrillization. A number of recent reports have indicated that these dye-binding assays could be prone to false positive effects when assessing inhibitors potential toward A beta peptides, species involved in Alzheimer's disease. Specifically, this review focuses on the application of thioflavin T for determining the efficiency of small, molecule inhibitors of A beta aggregation and addresses potential reasons that might be associated with the false positive effects in an effort to increase reliability of dye-binding assays.
引用
收藏
页码:807 / 819
页数:13
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