Noncompetitive Determination of Small Analytes by Sandwich-Type Lateral Flow Assay Based on an Aptamer Kissing Complex

被引:1
|
作者
Chovelon, Benoit [1 ,2 ,3 ]
Ranganathan, Velu [3 ]
Srinivasan, Sathya [3 ]
McConnell, Erin M. [3 ]
Faure, Patrice [1 ,2 ]
Fiore, Emmanuelle [1 ]
Ravelet, Corinne [1 ]
Peyrin, Eric [1 ]
DeRosa, Maria [3 ]
机构
[1] Univ Grenoble Alpes, DPM, CNRS, UMR 5063, F-38041 Grenoble, France
[2] Grenoble Site Nord CHU, Biol & Pathol Inst, Biochem Toxicol & Pharmacol Dept, F-38041 Grenoble, France
[3] Carleton Univ, Dept Chem, Ottawa, ON K1S 5B6, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
MOLECULE; APTASENSOR; SEPARATION; ADENOSINE; TARGETS; BINDING;
D O I
10.1021/acs.analchem.3c05472
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Here, we present the proof-of-concept of a lateral flow assay (LFA) that is capable of detecting small-molecule targets in a noncompetitive manner by deploying a sandwich-type format based on the aptamer kissing complex (AKC) strategy. A fluorescently labeled hairpin aptamer served as the signaling agent, while a specific RNA hairpin grafted onto the strip served as the capture element. The hairpin aptamer switched from an unfolded to a folded form in the presence of the target, resulting in kissing interactions between the loops of the reporter and the capture agents. This design triggered a target-dependent fluorescent signal at the test line. The AKC-based LFA was developed for the detection of adenosine, achieving a detection limit in the micromolar range. The assay revealed the presence of the same analyte in urine. The method also proved effective with another small molecule (theophylline). We believe that the AKC-based LFA approach could overcome many of the shortcomings associated with conventional signal-off methods and competitive processes.
引用
收藏
页码:6875 / 6880
页数:6
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