Enantioselective and label-free detection of oligopeptide via fluorescent indicator displacement

被引:8
|
作者
Ren, Jiangtao [1 ,2 ]
Wang, Jiahai [1 ]
Wang, Jin [1 ,3 ]
Luedtke, Nathan W. [4 ]
Wang, Erkang [1 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Electroanalyt Chem, Changchun 130022, Jilin, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 100039, Peoples R China
[3] SUNY Stony Brook, Dept Chem Phys & Appl Math, Stony Brook, NY 11794 USA
[4] Univ Zurich, Inst Organ Chem, CH-8057 Zurich, Switzerland
基金
中国国家自然科学基金;
关键词
Chiral discrimination; Enantiomer; DNA aptamer; Label-free; Fluorescent indicator; CHIRAL STATIONARY-PHASE; L-RNA APTAMER; HIV-1; ENTRY; AMINO-ACIDS; DNA APTAMER; TARGET; THALIDOMIDE; SEPARATION; ENANTIOSEPARATION; PHTHALOCYANINES;
D O I
10.1016/j.bios.2012.03.028
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
In this work, a simple and label-free fluorescent method via fluorescent indicator displacement (FID) was proposed for enantioselectively determining D-enantiomer of arginine vasopressin (DV) using DV-specific DNA aptamer (V-apt) and one guanidiniophthalocyanine dye (Zn-DIGP). Zn-DIGP that preferentially binds to single-stranded DNA with fluorescence enhancement rather than duplexes occupies the long internal loop of V-apt and generates intensive fluorescence. Then DV is introduced into the solution containing Zn-DIGP and V-apt, and displaces the Zn-DIGP from the binding site of internal loop, leading to fluorescence decrease. But L-enantiomer cannot induce any fluorescence change due to the selectivity of V-apt. This established FID technique can detect DV with a detection limit of 100 nM and exhibits a broad linear range, and is able to discriminate enantiomers of arginine vasopressin unambiguously. Moreover chiral separation by chromatography, complicated experimental procedures and covalent modification of tags (such as organic dyes, redox-active metal complexes) are avoided in our strategy. This simple and label-free method is promising for fabricating diverse aptasensors to determine other biomolecules and drugs. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:401 / 406
页数:6
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