Perylene ligand wrapping G-quadruplex DNA for label-free fluorescence potassium recognition

被引:20
作者
Hu, Yuwei [1 ,2 ]
Han, Dongxue [1 ]
Zhang, Qixian [1 ]
Wu, Tongshun [1 ]
Li, Fenghua [1 ]
Niu, Li [1 ,2 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Electroanalyt Chem, Engn Lab Modern Analyt Tech, Changchun 130022, Peoples R China
[2] Jilin Univ, Coll Chem, Changchun 130012, Peoples R China
关键词
Perylene; G-quadruplex; Potassium; Fluorescence; Label-free; 3,4,9,10-PERYLENETETRACARBOXYLIC ACID DIIMIDES; ENERGY-TRANSFER; CONJUGATED POLYMER; SIDE-CHAINS; ION; OLIGONUCLEOTIDE; AGGREGATION; SELECTIVITY; COMPLEX; BINDING;
D O I
10.1016/j.bios.2012.06.042
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
A perylene ligand, N,N-bis-(1-aminopropyl-3-propylimidazol salt)-3,4,9,10-perylene tetracarboxylic acid diimide ligand (PDI), which consisted of pi-conjugated perylene moiety and hydrophilic side chains with positively charged imidazole rings, was used to wrap G-quadruplex for fluorescence turn-on K+ recognition. Electrostatic attraction between PDI's positively charged imidazole rings and DNA's negatively charged phosphate backbones enabled PDI to accumulate on DNA. Upon trapping K+, these G-rich DNA sequences transitioned to G-quadruplex. Subsequently, PDI ligands wrapped G-quadruplex, in which the flat aromatic core of PDI ligand interacted with G-quartet through pi-pi stacking and the side chains were positioned in grooves through electrostatic interactions. Consequently, the interaction mode change and conformational transition from PDI stacked G-sequence to PDI wrapped G-quadruplex led to PDI fluorescence enhancement, which was readily monitored as the detection signal. This strategy excluded the sequence tagging step and exhibited high selectivity and sensitivity towards K+ ion with the linear detection range of 10-150 nM. Besides. PDI ligands may hold diagnostic and therapeutic application potentials to human telomere and cancer cells. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:396 / 401
页数:6
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