Coaxial sensing bio-amplifier for ultrasensitive detections of circulating tumor DNAs

Biosens Bioelectron. 2019 Sep 15:141:111414. doi: 10.1016/j.bios.2019.111414. Epub 2019 Jun 5.

Abstract

We herein report the first attempt to engineer a coaxial-sensing 3D amplifier able to achieve dynamic self-assembly in response to a mutated-ctDNA target. A bio-nanofiber is firstly manufactured via an ingenious double-channel electrostatic spinning and DNA rolling circle replication (RCR) technology, which offered an ideal scaffold for assembly of 3D amplifier activated by target recognition. The coaxial-controllable signal amplifier presented several advantages. (1) Given its "coaxial sensing effect", the proposed bio-amplifier played the coaxial transduction for signal enrichment to vastly increase sensitivity, capable of discriminating a single-base mismatched sequence from the perfectly complementary one, using ctDNA-134A as a model analyte. (2) Due to "covalent bridges lock effect" in an identifying chip with locked nucleic acid beacons, this 3D amplifier expressed high specificity and biostability toward seven different mutated-ctDNAs. (3) Profiting from special configuration of bioactive nanofibers and DNA replication programming, this catalytic bio-amplifier possessed "signal enrichment effect", which enhanced dynamic range toward ctDNA-134A detection and hybridized without any external indicators. This innovative bio-amplifier has a detection limit of 5.1 aM for ctDNA-134A with superior specificity, excellent sensitivity, and good performance. This pioneered method was further applied for broadly differentiate cells and evaluate changes in the expression levels of intracellular mutated-ctDNAs.

Keywords: 3D amplifier; Catalytic bio-nanofiber; Circulating tumor DNA; Coaxial sensing; DNA replication programming.

MeSH terms

  • Biosensing Techniques / methods*
  • Cell Line, Tumor
  • Circulating Tumor DNA / analysis*
  • Circulating Tumor DNA / genetics
  • Humans
  • Limit of Detection
  • Mutation
  • Nanofibers / chemistry
  • Nucleic Acid Amplification Techniques / methods
  • Oligonucleotide Array Sequence Analysis / instrumentation

Substances

  • Circulating Tumor DNA