Articles producció científica> Enginyeria Química

Exploiting the Nucleic Acid Nature of Aptamers for Signal Amplification

  • Dades identificatives

    Identificador: imarina:9286981
    Autors:
    Jauset-Rubio, MiriamOrtiz, MayreliO'Sullivan, Ciara K
    Resum:
    Aptamer-based assays and sensors are garnering increasing interest as alternatives to antibodies, particularly due to their increased flexibility for implementation in alternative assay formats, as they can be employed in assays designed for nucleic acids, such as molecular aptamer beacons or aptamer detection combined with amplification. In this work, we took advantage of the inherent nucleic acid nature of aptamers to enhance sensitivity in a rapid and facile assay format. An aptamer selected against the anaphylactic allergen β-conglutin was used to demonstrate the proof of concept. The aptamer was generated by using biotinylated dUTPs, and the affinity of the modified aptamer as compared to the unmodified aptamer was determined by using surface plasmon resonance to calculate the dissociation constant (KD), and no significant improvement in affinity due to the incorporation of the hydrophobic biotin was observed. The modified aptamer was then applied in a colorimetric competitive enzyme-linked oligonucleotide assay, where β-conglutin was immobilized on the wells of a microtiter plate, competing with β-conglutin free in solution for the binding to the aptamer. The limit of detection achieved was 68 pM, demonstrating an improvement in detection limit of three orders of magnitude as compared with the aptamer simply modified with a terminal biotin label. The concept was then exploited by using electrochemical detection and screen-printed electrodes where detection limits of 326 fM and 7.89 fM were obtained with carbon and gold electrodes, respectively. The assay format is generic in nature and can be applied to all aptamers, facilitating an easy and cost-effective means to achieve lower detection limits.
  • Altres:

    Autor segons l'article: Jauset-Rubio, Miriam; Ortiz, Mayreli; O'Sullivan, Ciara K
    Departament: Enginyeria Química
    Autor/s de la URV: Jauset Rubio, Miriam / O'SULLIVAN, CIARA KATHLEEN / Ortíz Rodríguez, Mayreli
    Paraules clau: High-affinity Enzyme-linked oligonucleotide assay (elona) Electrochemical detection Chronoamperometry Biotinylated dntps Aptasensors Aptamer rna probes nucleotides generation enzyme-linked oligonucleotide assay (elona) electrochemical detection dntps dna chronoamperometry biotinylated dntps binding avidin aptasensors
    Resum: Aptamer-based assays and sensors are garnering increasing interest as alternatives to antibodies, particularly due to their increased flexibility for implementation in alternative assay formats, as they can be employed in assays designed for nucleic acids, such as molecular aptamer beacons or aptamer detection combined with amplification. In this work, we took advantage of the inherent nucleic acid nature of aptamers to enhance sensitivity in a rapid and facile assay format. An aptamer selected against the anaphylactic allergen β-conglutin was used to demonstrate the proof of concept. The aptamer was generated by using biotinylated dUTPs, and the affinity of the modified aptamer as compared to the unmodified aptamer was determined by using surface plasmon resonance to calculate the dissociation constant (KD), and no significant improvement in affinity due to the incorporation of the hydrophobic biotin was observed. The modified aptamer was then applied in a colorimetric competitive enzyme-linked oligonucleotide assay, where β-conglutin was immobilized on the wells of a microtiter plate, competing with β-conglutin free in solution for the binding to the aptamer. The limit of detection achieved was 68 pM, demonstrating an improvement in detection limit of three orders of magnitude as compared with the aptamer simply modified with a terminal biotin label. The concept was then exploited by using electrochemical detection and screen-printed electrodes where detection limits of 326 fM and 7.89 fM were obtained with carbon and gold electrodes, respectively. The assay format is generic in nature and can be applied to all aptamers, facilitating an easy and cost-effective means to achieve lower detection limits.
    Àrees temàtiques: Química Nanoscience & nanotechnology Medicine (miscellaneous) Materiais Instruments & instrumentation Instrumentation Engineering (miscellaneous) Clinical biochemistry Ciencias sociales Ciências biológicas iii Ciências biológicas i Chemistry, analytical Biotecnología Biotechnology Biomedical engineering Astronomia / física Analytical chemistry
    Accès a la llicència d'ús: https://creativecommons.org/licenses/by/3.0/es/
    Adreça de correu electrònic de l'autor: mayreli.ortiz@urv.cat miriam.jauset@urv.cat mayreli.ortiz@urv.cat
    Identificador de l'autor: 0000-0002-9423-0055 0000-0002-9943-6132 0000-0002-9423-0055
    Data d'alta del registre: 2024-10-26
    Versió de l'article dipositat: info:eu-repo/semantics/publishedVersion
    Enllaç font original: https://www.mdpi.com/2079-6374/12/11/972
    URL Document de llicència: https://repositori.urv.cat/ca/proteccio-de-dades/
    Referència a l'article segons font original: Biosensors. 12 (11): 972-
    Referència de l'ítem segons les normes APA: Jauset-Rubio, Miriam; Ortiz, Mayreli; O'Sullivan, Ciara K (2022). Exploiting the Nucleic Acid Nature of Aptamers for Signal Amplification. Biosensors, 12(11), 972-. DOI: 10.3390/bios12110972
    DOI de l'article: 10.3390/bios12110972
    Entitat: Universitat Rovira i Virgili
    Any de publicació de la revista: 2022
    Tipus de publicació: Journal Publications
  • Paraules clau:

    Analytical Chemistry,Biomedical Engineering,Biotechnology,Chemistry, Analytical,Clinical Biochemistry,Instrumentation,Instruments & Instrumentation,Medicine (Miscellaneous),Nanoscience & Nanotechnology
    High-affinity
    Enzyme-linked oligonucleotide assay (elona)
    Electrochemical detection
    Chronoamperometry
    Biotinylated dntps
    Aptasensors
    Aptamer
    rna
    probes
    nucleotides
    generation
    enzyme-linked oligonucleotide assay (elona)
    electrochemical detection
    dntps
    dna
    chronoamperometry
    biotinylated dntps
    binding
    avidin
    aptasensors
    Química
    Nanoscience & nanotechnology
    Medicine (miscellaneous)
    Materiais
    Instruments & instrumentation
    Instrumentation
    Engineering (miscellaneous)
    Clinical biochemistry
    Ciencias sociales
    Ciências biológicas iii
    Ciências biológicas i
    Chemistry, analytical
    Biotecnología
    Biotechnology
    Biomedical engineering
    Astronomia / física
    Analytical chemistry
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