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Precisely Manipulating Steric Hindrance Effect on DNA Walker for Tunable Detection of MicroRNA Using Enzymatic Strand Displacement Amplification. | LitMetric

AI Article Synopsis

  • The study focuses on a new type of DNA walker that addresses the challenges posed by spatial constraints in its movement, specifically designed to detect microRNA-21 (miR-21).
  • It utilizes an enzymatic strand displacement amplification (ESDA) method that allows for adjustable sensitivity and detection limits by changing the lengths and sizes of DNA components.
  • The approach not only achieves effective detection of miR-21 in cancer cell samples but also holds potential for use in personalized medicine and early disease detection.

Article Abstract

The spatial constraints imposed by the DNA structure have significant implications for the walking efficiency of three-dimensional DNA walkers. However, accurately quantifying and manipulating steric hindrance remains a challenging task. This study presents a steric hindrance-controlled DNA walker utilizing an enzymatic strand displacement amplification (ESDA) strategy for detecting microRNA-21 (miR-21) with tunable dynamic range and sensitivity. The steric hindrance of the DNA walker was precisely manipulated by varying the length of empty bases from 6.5 Å to 27.4 Å at the end of the track strand and adjusting the volumetric dimensions of the hairpin structure from 9.13 nm to 26.2 nm at the terminus of the single-foot DNA walking strand. This method demonstrated a tunable limit of detection for miR-21 ranging from 3.6 aM to 35.6 nM, along with a dynamic range from ∼100-fold to ∼166 000-fold. Impressively, it exhibited successful identification of cancer cells and clinical serum samples with high miR-21 expression. The proposed novel strategy not only enables tunable detection of miRNA through the regulation of steric hindrance but also achieves accurate and quantitative analysis of the steric hindrance effect, promising broader applications in personalized medicine, early disease detection, and drug development.

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Source
http://dx.doi.org/10.1021/acs.analchem.4c02565DOI Listing

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