Aptamers are synthetic single-stranded nucleic acid molecules that bind to biochemical targets with high affinity and specificity. The method of systematic evolution of ligands by exponential enrichment (SELEX) is widely used to isolate aptamers from randomized oligonucleotides. Recently, microfluidic technology has been applied to improve the efficiency and reduce the cost in SELEX processes. In this work, we present an approach that exploits surface acoustic waves to improve the affinity selection process in microfluidic SELEX. Acoustic streaming is used to enhance the interactions of the solution-based oligonucleotide molecules with microbead-immobilized target molecules, allowing the identification of high-affinity aptamer candidates in a more efficient manner. For demonstration, a DNA aptamer is isolated within three rounds of selection in 5 h to specifically bind to immunoglobulin E, a representative target protein, with an equilibrium dissociation constant of approximately 22.6 nM.
Keyphrases
- nucleic acid
- label free
- circulating tumor cells
- high throughput
- single cell
- gold nanoparticles
- magnetic nanoparticles
- sensitive detection
- double blind
- open label
- photodynamic therapy
- cross sectional
- molecular dynamics simulations
- randomized controlled trial
- phase iii
- binding protein
- capillary electrophoresis
- mass spectrometry
- study protocol
- structural basis