Abstract

Signal transduction based on fluorescence is one of the most common optical aptasensors for small molecules. Sensors with a number of unique features including high sensitivity, low cost, and simple operation can be constructed easily. However, the label-free fluorescent approach is limited to synthetic dyes that bind strongly to the aptamer sequence and result in a diminished sensor operation with high detection limits. In this study, we report the use of curcumin as a fluorescent probe to signal aptamer/small target binding events. A substantial enhancement in curcumin’s fluorescent emission was observed when bound into the grooves of vitamin D3 (VTD3) binding aptamer, as an example. However, the introduction of the target molecule causes the aptamer to undergo a conformational change that favors complexing the target molecule over binding the curcumin dye. The sensor was able to detect VTD3 down to 1 fM concentration in buffer solutions and extracted blood samples, operate at a wide dynamic range, and discriminate against potential biological interfering molecules including VTD2. The operation of the curcumin based fluorescent sensor is at least six orders of magnitude more sensitive than a VTD3 sensor constructed with the synthetic dye SYBR Green I. The generality of the reported label-free approach was applied with a previously isolated 75-mer bisphenol-A (BPA) aptamer, confirming that the reported sensing strategy is not confined on a particular aptamer sequence. Our work not only reports a novel sensor format for the detection of small molecules, but also serves fluorescent sensor’s most pressing need being novel fluorophores for multiplex targets detection.

Highlights

  • Aptamers are short single stranded oligonucleotides (RNA or DNA) evolved through a combinatorial in vitro chemical process known as systematic evolution of ligands by exponential enrichment (SELEX) [1,2]

  • Is the predominant target molecule for emerging synthetic and natural drugs, many studies have characterized the binding mechanism of curcumin to DNA [46,47,48]. These studies concluded that: (1) The DNA curcumin binding could be groove, or intercalative; (2) DNA double helix is essential for curcumin interaction, (3) sodium ions are essential for the DNA–curcumin complex formation, and (4) the formation of the DNA–curcumin complex resulted in an enhancement of light absorption and emission of the curcumin molecule [46,47,48]

  • The seven-carbon spacer contains two α, β-unsaturated carbonyl groups that undergoes keto–enol tautomerism, which is the favorable state for binding with macromolecules including DNA [45,49]. All of these properties encouraged the construction of an effective hypothesis that curcumin is a potential aptasensor probe for small molecules

Read more

Summary

Introduction

Aptamers are short single stranded oligonucleotides (RNA or DNA) evolved through a combinatorial in vitro chemical process known as systematic evolution of ligands by exponential enrichment (SELEX) [1,2]. Aptamers can sensitively and selectively bind to a wide range of targets including metal ions [3], small molecules [4,5], and large targets [6]. Compared with the conventional recognition tools such as antibodies and enzymes in designing biosensors, aptamers exhibit a robust and low production method, low molecular weight, easy modification, and operation in non-immunogenic environments [10]. They are highly regarded as excellent candidates for developing biosensors for targets of medical, environmental, and industrial significance [11]. Due to Sensors 2019, 19, 4181; doi:10.3390/s19194181 www.mdpi.com/journal/sensors

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call