Dual catalytic DNA circuit-induced gold nanoparticle aggregation: An enzyme-free and colorimetric strategy for amplified detection of nucleic acids

Int J Biol Macromol. 2020 Jul 1:154:896-903. doi: 10.1016/j.ijbiomac.2020.03.059. Epub 2020 Mar 10.

Abstract

An enzyme-free dual catalytic DNA circuit for amplified detection of nucleic acids has been developed. The system functions based on a cyclic self-assembly of two auxiliary hairpins (H1 and H2) and three biotinylated hairpin oligonucleotides (H3, H4 and H5), in the format of two molecular circuits. In the upstream circuit, a target initiator (I) besides H1 and H2 hairpins constructs H1-H2 duplexes that trigger the operation of a subsequent circuit. In the downstream circuit, the H1-H2 duplex initiates cascaded self-assembly reactions, produces triplex H3-H4-H5, as sensing system, and releases the H1-H2 duplex as the catalyst for the self-assembly of additional hairpins. The H3-H4-H5 triplex acts as the scaffolds for assembling and orienting the streptavidin-functionalized gold nanoparticles (SA-AuNPs) into a lattice-like arrangement that generates a DNA-SA-AuNP cross-linked network, resulting in a dramatic pale red-to-blue color change. By ingeniously engaging two catalytic circuits with feedback amplification capabilities, the system can detect the target nucleic acid with an LOD value of 5 femtomolar and unambiguously discriminate spurious targets (i.e. targets containing substitution, insertion, and deletion nucleotides) without instrumentation. Simple and convenient operation of the assay makes the DNA circuit appropriate for point-of-care monitoring in resource-constrained settings.

Keywords: Colorimetric detection; DNA circuit; Gold nanoparticle; Hairpin assembly; Nucleic acid detection; Signal amplification.

MeSH terms

  • Biosensing Techniques*
  • Colorimetry*
  • DNA / analysis*
  • DNA, Catalytic / chemistry*
  • Gold / chemistry*
  • Inverted Repeat Sequences
  • Metal Nanoparticles / chemistry*

Substances

  • DNA, Catalytic
  • Gold
  • DNA