Naked Eye Y Amelogenin Gene Fragment Detection Using DNAzymes on a Paper-based Device

Nowadays, there are strong efforts in developing new technology for rapid detection of specific DNA sequences for environmental monitoring, forensic analysis and rapid biomedical diagnosis applications. That is where microfluidic paper-based analytical devices are positioned as suitable platforms fo...

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Detalles Bibliográficos
Autores: Azuaje Hualde, Enrique, Arroyo Jiménez, Susana, Garai Ibabe, Gaizka, Benito López, Fernando, Martínez de Pancorbo Gómez, María de los Angeles
Tipo de recurso: artículo
Fecha de publicación:2020
País:España
Institución:Universidad del País Vasco
Repositorio:Addi. Archivo Digital para la Docencia y la Investigación
OAI Identifier:oai:addi.ehu.eus:10810/43659
Acceso en línea:http://hdl.handle.net/10810/43659
Access Level:acceso abierto
Palabra clave:DNAzyme, amelogenin, paper substrate, gene detection, colorimetric, paper based microfluidics
DNAzyme
amelogenin
paper substrate
gene detection
colorimetric
paper based microfluidics
Descripción
Sumario:Nowadays, there are strong efforts in developing new technology for rapid detection of specific DNA sequences for environmental monitoring, forensic analysis and rapid biomedical diagnosis applications. That is where microfluidic paper-based analytical devices are positioned as suitable platforms for the development of point of care analytical devices, due to their simple fabrication protocols, ease of use and low cost. Herein, a methodology for in situ single strand DNA detection by using a colorimetric assay based on the formation of a DNAzyme within a paper substrate was developed. A DNAzyme that could only be formed in the presence of a specific sequence of the Y human amelogenin gene was designed. The performance of the DNAzyme was followed colorimetrically first in solution and then in paper substrates. The reaction was found to be specific to the Y fragment selected as analyte. The DNAzyme reaction on paper enabled the unequivocal colorimetric identification of the Y single strand DNA fragment both qualitatively, with the naked eye (143 ng), and quantitatively by image analysis (45.7 ng). As a proof of concept, a microfluidic paper-based device, pre-loaded with all DNAzyme reagents, was characterized and implemented for the simultaneous detection of X and Y single strand DNA fragments.