Understanding FRET in Upconversion Nanoparticle Nucleic Acid Biosensors.
basic_science · Level V
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- Record sourced from PubMed, PMID 36729707.
- Also identified by DOI 10.1021/acs.nanolett.2c04899.
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Abstract
Upconversion nanoparticles (UCNPs) have been frequently applied in Förster resonance energy transfer (FRET) bioanalysis. However, the understanding of how surface coatings, bioconjugation, and dye-surface distance influence FRET biosensing performance has not significantly advanced. Here, we investigated UCNP-to-dye FRET DNA-hybridization assays in H<sub>2</sub>O and D<sub>2</sub>O using ∼24 nm large NaYF<sub>4</sub>:Yb<sup>3+</sup>,Er<sup>3+</sup> UCNPs coated with thin layers of silica (SiO<sub>2</sub>) or poly(acrylic acid) (PAA). FRET resulted in strong distance-dependent PL intensity changes. However, the PL decay times were not significantly altered because of continuous Yb<sup>3+</sup>-to-Er<sup>3+</sup> energy migration during Er<sup>3+</sup>-to-dye FRET. Direct bioconjugation of DNA to the thin PAA coating combined with the closest possible dye-surface distance resulted in optimal FRET performance with minor influence from competitive quenching by H<sub>2</sub>O. The better comprehension of UCNP-to-dye FRET was successfully translated into a microRNA (miR-20a) FRET assay with a limit of detection of 100 fmol in a 80 μL sample volume.
Medical subject headings
- Nucleic Acids
- Nanoparticles
- Biosensing Techniques