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Noncompetitive Determination of Small Analytes by Sandwich-Type Lateral Flow Assay Based on an Aptamer Kissing Complex.
Chovelon, Benoit; Ranganathan, Velu; Srinivasan, Sathya; McConnell, Erin M; Faure, Patrice; Fiore, Emmanuelle; Ravelet, Corinne; Peyrin, Eric; DeRosa, Maria.
Afiliación
  • Chovelon B; University Grenoble Alpes, DPM UMR 5063, CNRS, F-38041 Grenoble, France.
  • Ranganathan V; Biochemistry, Toxicology and Pharmacology Department, Grenoble Site Nord CHU-Biology and Pathology Institute, F-38041 Grenoble, France.
  • Srinivasan S; Department of Chemistry, Carleton University, 1125 Colonel By Drive, Ottawa, Ontario K1S 5B6, Canada.
  • McConnell EM; Department of Chemistry, Carleton University, 1125 Colonel By Drive, Ottawa, Ontario K1S 5B6, Canada.
  • Faure P; Department of Chemistry, Carleton University, 1125 Colonel By Drive, Ottawa, Ontario K1S 5B6, Canada.
  • Fiore E; Department of Chemistry, Carleton University, 1125 Colonel By Drive, Ottawa, Ontario K1S 5B6, Canada.
  • Ravelet C; University Grenoble Alpes, DPM UMR 5063, CNRS, F-38041 Grenoble, France.
  • Peyrin E; Biochemistry, Toxicology and Pharmacology Department, Grenoble Site Nord CHU-Biology and Pathology Institute, F-38041 Grenoble, France.
  • DeRosa M; University Grenoble Alpes, DPM UMR 5063, CNRS, F-38041 Grenoble, France.
Anal Chem ; 96(18): 6875-6880, 2024 05 07.
Article en En | MEDLINE | ID: mdl-38651263
ABSTRACT
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.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Técnicas Biosensibles / Adenosina / Aptámeros de Nucleótidos Límite: Humans Idioma: En Revista: Anal Chem Año: 2024 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Técnicas Biosensibles / Adenosina / Aptámeros de Nucleótidos Límite: Humans Idioma: En Revista: Anal Chem Año: 2024 Tipo del documento: Article País de afiliación: Francia
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