Magnetic Beads-Based Sensor with Tailored Sensitivity for Rapid and Single-Step Amperometric Determination of miRNAs.
Eva VargasRebeca M Torrente-RodríguezVíctor Ruiz-Valdepeñas MontielEloy PovedanoMaría PedreroJuan J MontoyaSusana CampuzanoJosé Manuel PingarrónPublished in: International journal of molecular sciences (2017)
This work describes a sensitive amperometric magneto-biosensor for single-step and rapid determination of microRNAs (miRNAs). The developed strategy involves the use of direct hybridization of the target miRNA (miRNA-21) with a specific biotinylated DNA probe immobilized on streptavidin-modified magnetic beads (MBs), and labeling of the resulting heteroduplexes with a specific DNA-RNA antibody and the bacterial protein A (ProtA) conjugated with an horseradish peroxidase (HRP) homopolymer (Poly-HRP40) as an enzymatic label for signal amplification. Amperometric detection is performed upon magnetic capture of the modified MBs onto the working electrode surface of disposable screen-printed carbon electrodes (SPCEs) using the H₂O₂/hydroquinone (HQ) system. The magnitude of the cathodic signal obtained at -0.20 V (vs. the Ag pseudo-reference electrode) demonstrated linear dependence with the concentration of the synthetic target miRNA over the 1.0 to 100 pM range. The method provided a detection limit (LOD) of 10 attomoles (in a 25 μL sample) without any target miRNA amplification in just 30 min (once the DNA capture probe-MBs were prepared). This approach shows improved sensitivity compared with that of biosensors constructed with the same anti-DNA-RNA Ab as capture instead of a detector antibody and further labeling with a Strep-HRP conjugate instead of the Poly-HRP40 homopolymer. The developed strategy involves a single step working protocol, as well as the possibility to tailor the sensitivity by enlarging the length of the DNA/miRNA heteroduplexes using additional probes and/or performing the labelling with ProtA conjugated with homopolymers prepared with different numbers of HRP molecules. The practical usefulness was demonstrated by determination of the endogenous levels of the mature target miRNA in 250 ng raw total RNA (RNAt) extracted from human mammary epithelial normal (MCF-10A) and cancer (MCF-7) cells and tumor tissues.
Keyphrases
- nucleic acid
- single molecule
- circulating tumor
- molecularly imprinted
- cell free
- label free
- hydrogen peroxide
- loop mediated isothermal amplification
- living cells
- reduced graphene oxide
- quantum dots
- solid phase extraction
- randomized controlled trial
- endothelial cells
- air pollution
- computed tomography
- gene expression
- breast cancer cells
- nitric oxide
- induced apoptosis
- carbon nanotubes
- risk assessment
- squamous cell carcinoma
- circulating tumor cells
- small molecule
- photodynamic therapy
- papillary thyroid
- cancer therapy
- squamous cell
- heavy metals
- magnetic nanoparticles
- simultaneous determination
- oxidative stress
- cell cycle arrest
- single cell
- fluorescent probe
- contrast enhanced