Binary Malachite Green Aptamer for Fluorescent Detection of Nucleic Acids

Dmitry M. Kolpashchikov

Journal of the American Chemical Society · 2005 · 215 citations · 11 references

TL;DR

A probe was developed to fluorescently detect specific nucleic acids in solution with extremely high selectivity. The probe comprises malachite green dye and two short RNA strands that assemble into a malachite green aptamer upon hybridization to the target, enabling dye binding and fluorescence enhancement. The probe discriminates 41 of 42 single‑nucleotide substitutions in a 14‑mer DNA analyte at room temperature in physiological buffer and, being composed of unmodified RNA strands, is suitable for real‑time in‑vivo nucleic acid monitoring.

Abstract

A new probe that can fluorescently report the presence of specific nucleic acids in solution with extremely high selectivity was developed. The probe consists of malachite greena triphenylmethane dyeand two short RNA strands, each of which comprises a fragment complementary to an analyte molecule and a fragment of a malachite green aptamer (MGA). The two RNA strands form MGA upon hybridization to the adjacent positions of the nucleic acid analyte. MGA is able to bind malachite green and enhance the fluorescence of the dye, thus monitoring the presence of the nucleic acid in solution. The probe reliably discriminates against 41 out of 42 possible single nucleotide substitutions in 14-mer DNA analyte at room temperature in physiological buffer. Consisting of unmodified RNA strands, which can be expressed in living cells, binary MGA probe represents a promising instrument for real-time nucleic acid monitoring in vivo.

References

11