Switchable inhibitory behavior of divalent magnesium ion in DNA hybridization-based gene quantification

Abstract

Contrary to the understanding that divalent cations only result in under-estimation of gene quantification via DNA hybridization-based assays, we have discovered that Mg²⁺ could cause either under or over-estimation at different concentrations. Its switchable inhibitory behavior is likely due to its rigid first solvation (hydrated) shell and hence it is inclined to form non-direct binding with DNA. At low concentrations, it caused under-estimation by occupying the hybridization sites. At high concentrations, it caused probe, signaling and target DNA to aggregate non-specifically via Coulomb forces. By quantifying target DNAs at a range of Mg²⁺ concentrations using a gene quantification assay (NanoGene assay), a Mg²⁺ inflection concentration of ∼10⁻³ M was observed for both target ssDNA and dsDNA. Field emission scanning electron microscopy (FE-SEM), energy dispersive X-ray spectroscopy (EDS), and Fourier transform infrared spectroscopy (FT-IR) were employed to observe Mg²⁺-induced non-specific binding in the complexes that mimicked the presence of target DNA. Together with two other divalent cations Ca²⁺ and Cu²⁺, they were further examined via zeta potential measurements as well as NanoGene assay. This study revealed the importance of Mg²⁺ in achieving accurate gene quantification. Through a better mechanistic understanding of this phenomenon, it will be possible to develop strategies to mitigate the impact of Mg²⁺ on DNA hybridization-based gene quantification.