Diphenylalanin nanofibers-inspired synthesis of fluorescent gold nanoclusters for screening of anti-amyloid drugs

被引:4
作者
Zohrabi, Tayebeh [1 ]
Amiri-Sadeghan, Amir [2 ]
Ganjali, Mohammad Reza [3 ]
Hosseinkhani, Saman [4 ]
机构
[1] Tarbiat Modares Univ, Fac Biol Sci, Dept Nanobiotechnol, Tehran, Iran
[2] Tabriz Univ Med Sci, TB & Lung Dis Res Ctr, Tabriz, Iran
[3] Univ Tehran, Ctr Excellence Electrochem, Tehran, Iran
[4] Tarbiat Modares Univ, Fac Biol Sci, Dept Biochem, Tehran, Iran
关键词
nanobiosensor; FF peptide; nanoclusters; drug screening; fluorometric assay; anti-amyloid drug; THIOFLAVIN-T-BINDING; ALZHEIMERS-DISEASE; ALPHA-SYNUCLEIN; METHYLENE-BLUE; AGGREGATION; CURCUMIN; FIBRILS; MECHANISM; INHIBITORS; INSIGHTS;
D O I
10.1088/2050-6120/ab9fef
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Protein misfolding and aggregation into amyloid structures is linked with a number of pathophysiological disorders. In the past decade, significant progresses have been made in the drug discovery strategies against toxic aggregates. Although lack of specificity and high sensitivity forin vitroscreening system still seen. Here we demonstrate a new targeting probe based on FF diphenylalanine peptide -protected gold nanoclusters (FF AuNCs). Diphenylalanine peptide has previously been shown to self-assemble into well-ordered fiber like the fibers that are observed in amyloid aggregates. We used of the self-assembly properties along with the ability of FF dipeptide in reduction of gold ions for synthesis of novel Au nanoclusters. We used FF AuNCs for monitoring of effectiveness of anti-amyloid drugs. Fluorescence was considerably diminished when drugs at different concentrations added, due to destruction of the amyloid fibers. Furthermore, the analysis of several components demonstrates significant selectivity against the amyloid disrupting molecules. Prepared FF AuNCs will gain possible strategy forin vitroscreening of amyloid disrupting molecules.
引用
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页数:11
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