4.7 Article

Combination of ferrocene decorated gold nanoparticles and engineered primers for the direct reagentless determination of isothermally amplified DNA

Journal

MICROCHIMICA ACTA
Volume 188, Issue 4, Pages -

Publisher

SPRINGER WIEN
DOI: 10.1007/s00604-021-04771-8

Keywords

DNA detection; Modified primers; Functionalized gold nanoparticles; Electrochemical detection; Isothermal amplification; Recombinase polymerase amplification; Karlodinium armiger sequence in seawater

Funding

  1. Spanish Ministerio de Economia y Competitividad [SEASENSING BIO2014-56024-C21]

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A reagent-less DNA sensor utilizing gold nanoparticles, modified primers, and isothermal amplification has been developed and successfully applied for the detection of Karlodinium armiger. The sensor demonstrates high sensitivity and rapid detection speed through optimized reaction conditions.
A reagent-less DNA sensor has been developed exploiting a combination of gold nanoparticles, modified primers, and isothermal amplification. It is applied to the determination ofKarlodinium armiger, a toxic microalgae, as a model analyte to demonstrate this generic platform. Colloidal gold nanoparticles with an average diameter of 14 +/- 0.87 nm were modified with a mixed self-assembled monolayer of thiolated 33-mer DNA probes and (6-mercaptohexyl) ferrocene. Modified primers, exploiting a C3 spacer between the primer-binding site and an engineered single-stranded tail, were used in an isothermal recombinase polymerase amplification reaction to produce an amplicon by two single-stranded tails. These tails were designed to be complementary to a gold electrode tethered capture oligo probe, and an oligo probe immobilized on the gold nanoparticles, respectively. The time required for hybridization of the target tailed DNA with the surface immobilized probe and reporter probe immobilized on AuNPs was optimized and reduced to 10 min, in both cases. Amplification time was further optimized to be 40 min to ensure the maximum signal. Under optimal conditions, the limit of detection was found to be 1.6 fM of target dsDNA. Finally, the developed biosensor was successfully applied to the detection of genomic DNA extracted from a seawater sample that had been spiked with K. armiger cells. The demonstrated generic electrochemical genosensor can be exploited for the detection of any DNA sequence and ongoing work is moving towards an integrated system for use at the point-of-need.

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