In vitro selection of RNA aptamers that selectively bind danofloxacin

• Published in: Biochemical and biophysical research communications Vol. 448; no. 4; pp. 397 - 402
• Main Authors: Han, Seung Ryul, Yu, Jaehoon, Lee, Seong-Wook
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 13.06.2014
• Subjects: Animal Husbandry; Animals; Anti-Bacterial Agents - analysis; Anti-Bacterial Agents - metabolism; Anti-Bacterial Agents - toxicity; Aptamers, Nucleotide - chemistry; Aptamers, Nucleotide - genetics; Aptamers, Nucleotide - metabolism; Base Sequence; Danofloxacin; Drug Residues - analysis; Drug Residues - metabolism; Drug Residues - toxicity; Fluoroquinolones - analysis; Fluoroquinolones - metabolism; Fluoroquinolones - toxicity; Food Contamination - analysis; Humans; Nucleic Acid Conformation; RNA aptamer; SELEX; SELEX Aptamer Technique - methods; Surface Plasmon Resonance; RNA aptamer; Danofloxacin; SELEX
• ISSN: 0006-291X; 1090-2104
• DOI: 10.1016/j.bbrc.2014.04.103

•Identification of RNase-resistant RNA aptamers to danofloxacin using SELEX.•High affinity and specificity to danofloxacin by the selected RNA aptamers.•Minimizing the aptamer up to 36mer without compromising affinity and specificity.•High discrimination of danofloxacin from other fluoroquinolones by the aptamer. Danofloxacin is a synthetic fluoroquinolone with broad spectrum antibacterial activity that is used for the treatment of respiratory diseases in animal husbandry. However, danofloxacin has many adverse reactions and is toxic to humans. Especially, it detrimentally affects muscle, central nerve system, peripheral nerve system, liver, and skin in those who ingest foods in which danofloxacin has accumulated. Prescreening and determination of the level of danofloxacin in foods or food products is necessary for human health. Aptamers are composing of oligonucleotides that specifically interact with target molecules. They are emerging as detection/diagnostic ligands. Here, we used the SELEX in vitro selection technology to identify specific and high-affinity RNA aptamers with 2′-fluoro-2′-deoxyribonucleotide modified pyrimidine nucleotides against danofloxacin. Selected RNA aptamers bound specifically to danofloxacin, but not to tetracycline. Truncation of RNA aptamer up to 36mer did not comprise specificity and affinity. The truncated RNA aptamer specifically bound to target chemical, allowing the discrimination of danofloxacin from other fluoroquinolones. The isolated specific aptamer could be a potential agent used for the rapid and cost-effective detection and sensing of danofloxacin, replacing instrumental methods including the more expensive and time-consuming methods of high performance liquid chromatography and liquid chromatography/mass spectrometry.