Highly selective fluorescent peptide-based chemosensors for aluminium ions in aqueous solution

被引:9
作者
Ramezanpour, Sorour [1 ]
Barzinmehr, Hamed [1 ]
Shiri, Pezhman [1 ]
Meier, Chris [2 ]
Ayatollahi, Seyed Abdulmajid [3 ]
Mehrazar, Mehrdad [1 ]
机构
[1] KN Toosi Univ Technol, Dept Chem, POB 15875-4416, Tehran, Iran
[2] Univ Hamburg, Martin Luther King Pl 6, D-20146 Hamburg, Germany
[3] Shahid Beheshti Univ Med Sci, Phytochem Res Ctr, Tehran 1434875451, Iran
基金
美国国家科学基金会;
关键词
Chemosensor; Peptide; Fluorophore; Aluminium; Fluorescence; METAL; SENSOR;
D O I
10.1007/s00216-021-03339-y
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Two novel fluorescent peptide-based chemosensors, including A (2-amino-benzoyl-Ser-Glu-Glu-NH2) and B (2-amino-benzoyl-Ala-Glu-Pro-Glu-Ala-Glu-Pro-NH2) were synthesized and characterized by nuclear magnetic resonance (NMR) spectra. These fluorescent probes exhibited excellent selective and sensitive responses to Al3+ ions over other metal ions in aqueous buffered solutions. The limits of detection for both chemosensors towards the Al3+ ions were in the order of similar to 10(-7) M (A: 155 nM and B: 195 nM), which clearly indicates that these probes have significant potential for biological applications. They also displayed high binding affinity (1.3029 x 10(4) M-1 and 1.7586 x 10(4) M-1 relevant to A and B respectively). These two chemosensors are great analytical probes that produce turn-on responses upon binding to Al3+ ions through an intramolecular charge transfer (ICT) mechanism. In addition, the application of both chemosensors was examined over a wide range of pH. The fluorescent peptide-based probes and Al3+ form a 1:1 coordination complex according to the ESI-MS and Job's plot analysis. Notably, upon addition of Al3+ to these chemosensors, a fluorescence enhancement of approximately 8-fold was observed and the binding mode was determined using NMR titration and fluorescence emission data.
引用
收藏
页码:3881 / 3891
页数:11
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