Selective recognition of tryptophan by a methylpillar[5]arene-based supramolecular fuorescent probe

被引:15
作者
Zhu, Xinyi [1 ]
Zhao, Jie [1 ]
Dai, Feifei [2 ]
Xu, Weitao [1 ]
Chen, Lixia [1 ]
Xiao, Xin [1 ]
Tao, Zhu [1 ]
Zhang, Chao [1 ]
机构
[1] Guizhou Univ, Key Lab Macrocycl & Supramol Chem Guizhou Prov, Guiyang 550025, Peoples R China
[2] Taizhou Inst Prod Qual & Safety Inspect, Taizhou 318000, Peoples R China
基金
中国国家自然科学基金;
关键词
Amino acids; Methylpillar[5]arene (MeP5); Host-guest chemistry; Self-assembled architectures; AGGREGATION-INDUCED EMISSION; HOST-GUEST INTERACTION; AMINO-ACIDS; FLUORESCENT; POLYMERS; BINDING; SENSOR; CONSTRUCTION; CHEMOSENSOR; CHIRALITY;
D O I
10.1016/j.saa.2020.119381
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
Herein we present a simple fluorescence quenching method to selectively recognise and determine Ltryptophan (L-Trp) out of other 19 natural amino acids. Methylpillar[5]arene (MeP5), which is employed as a macrocyclic fluorescent probe, exhibits fluorescence activity in the solution of poor solvents because of aggregation-induced emission (AIE) effect. Fluorescence quenching of MeP5 in the solution of EtOH/ CH2Cl2 (98/2, v/v) was observed upon the addition of L-Trp whereas other 19 natural amino acids did not bring about obvious change in fluorescence intensity. H-1 NMR titration, fluorescence spectroscopy, mass spectrometry and theoretical analysis revealed that L-Trp can be encapsulated into the cavity of MeP5 to form a stable 1:1 host-guest inclusion complex which accounts for the quenching characteristics. The proposed procedure in this investigation offers an attractive and promising method for the selective detection of L-Trp in a mixture of natural amino acids. (C) 2020 Elsevier B.V. All rights reserved.
引用
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页数:6
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