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Selection and characterisation of triclosan-specific aptamers using a fluorescence microscope-imaging assay

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Abstract

This study reports a fluorescence microscope-imaging assay for determining the binding characteristics of single-stranded DNA aptamers selected against the antibacterial agent, triclosan. The imaging assay utilises fluorescently labelled aptamers and target-immobilised matrices. Upon binding of triclosan-specific aptamers to triclosan-conjugated matrices, the binding complex was visualised and the image was captured with the aid of a fluorescence microscope. Subsequently, the fluorescent intensities of aptamer-bound matrices were analysed using dedicated image-processing software and correlated to known concentrations of selected input aptamers. Thus, by plotting fluorescence intensities against different aptamer concentrations, binding isotherms were generated to determine aptamer Kd values. The imaging assay was applied to characterise the binding affinities and specificities of ten triclosan-specific aptamers H1–H10. One of the candidate aptamers, H6, showed a Kd value of 378 nM, which was comparable with previously published Kd values for aptamer—generated against triclosan analogous. In addition, the utility of the imaging assay for aptamer characterisation was compared with a commonly used affinity column-binding assay. It was concluded that the imaging assay was superior to alternative assays in terms of accuracy, simplicity, and reproducibility.

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References

  1. Dann AB, Hontela A. Triclosan: environmental exposure, toxicity and mechanisms of action. J Appl Toxicol. 2011;31:285–311.

    Article  CAS  Google Scholar 

  2. Zhao C, Xie H, Xu J, Xu X, Zhang J, Hu Z, et al. Bacterial community variation and microbial mechanism of triclosan (TCS) removal by constructed wetlands with different types of plants. Sci Total Environ. 2015;505:633–9.

    Article  CAS  Google Scholar 

  3. Wang H, Zhang J, Gao F, Yang Y, Duan H, Wu Y, et al. Simultaneous analysis of synthetic musks and triclosan in human breast milk by gas chromatography tandem mass spectrometry. J Chromatogr B. 2011;879:1861–9.

    Article  CAS  Google Scholar 

  4. Azzouz A, Rascón AJ, Ballesteros E. Simultaneous determination of parabens, alkylphenols, phenylphenols, bisphenol A and triclosan in human urine, blood and breast milk by continuous solid-phase extraction and gas chromatography–mass spectrometry. J Pharm Biomed Anal. 2016;119:16–26.

    Article  CAS  Google Scholar 

  5. Asimakopoulos AG, Wang L, Thomaidis NS, Kannan K. A multi-class bioanalytical methodology for the determination of bisphenol A diglycidyl ethers, P-hydroxybenzoic acid esters, benzophenone-type ultraviolet filters, triclosan, and triclocarban in human urine by liquid chromatography–tandem mass spectrometry. J Chromatogr A. 2014;1324:141–8.

    Article  CAS  Google Scholar 

  6. Henry ND, Fair PA. Comparison of in vitro cytotoxicity, estrogenicity and anti-estrogenicity of triclosan, perfluorooctane sulfonate and perfluorooctanoic acid. J Appl Toxicol. 2013;33:265–72.

    Article  Google Scholar 

  7. Kumar V, Chakraborty A, Kural MR, Roy P. Alteration of testicular steroidogenesis and histopathology of reproductive system in male rats treated with triclosan. Reprod Toxicol. 2019;27:177–85.

    Article  Google Scholar 

  8. Yueh MF, Taniguchi K, Chen S, Evans RM, Hammock BD, Karin M, et al. The commonly used antimicrobial additive triclosan is a liver tumor promoter. Proc Natl Acad Sci. 2014;111:17200–5.

    Article  CAS  Google Scholar 

  9. Li S. Selection and characterisation of single-stranded DNA aptamers for triclosan. A PhD thesis submitted to the library of Victoria University of Wellington, New Zealand. 2016;URI:http://hdl.handle.net/10063/5017.

  10. Ahn KC, Ranganathan A, Bever CS, Hwang SH, Holland EB, Morisseau K, et al. Detection of the antimicrobial triclosan in environmental samples by immunoassay. Environ Sci Technol. 2016;50:3754–61.

    Article  CAS  Google Scholar 

  11. Cha M, Lee HJ, Kim JS, Kim E. Environmental assessment of estrogenic pollutants in Nam River of Korea using indirect competitive Elisa and E-screen assay. Toxicol Environ Heal Sci. 2013;4:262–8.

    Article  Google Scholar 

  12. Ellington AD, Szostak JW. In vitro selection of RNA molecules that bind specific ligands. Nature. 1990;346:818–22.

    Article  CAS  Google Scholar 

  13. Tuerk C, Gold L. Systematic evolution of ligands by exponential enrichment - RNA ligands to bacteriophage-T4 DNA-polymerase. Science. 1990;249:505–10.

    Article  CAS  Google Scholar 

  14. Alsager OA, Kumar S, Zhu B, Travas-Sejdic J, McNatty KP, Hodgkiss JM. Ultrasensitive colorimetric detection of 17β-estradiol: the effect of shortening DNA aptamer sequences. Anal Chem. 2015;87:4201–9.

    Article  CAS  Google Scholar 

  15. Cruz-Aguado JA, Penner G. Fluorescence polarization based displacement assay for the determination of small molecules with aptamers. Anal Chem. 2008;80:8853–5.

    Article  CAS  Google Scholar 

  16. Mehta J, Rouah-Martin E, Van Dorst B, Maes B, Herrebout W, Scippo ML, et al. Selection and characterization of PCB-binding DNA aptamers. Anal Chem. 2012;84:1669–76.

    Article  CAS  Google Scholar 

  17. Ma H, Liu J, Ali MM, Mahmood MA, Labanieh L, Lu M, et al. Nucleic acid aptamers in cancer research, diagnosis and therapy. Chem Soc Rev. 2015;44:1240–56.

    Article  CAS  Google Scholar 

  18. Sundberg L, Porath J. Preparation of adsorbents for biospecific affinity chromatography. 1. Attachment of group-containing ligands to insoluble polymers by means of bifunctional oxiranes. J Chromatogr A. 1974;90:87–98.

    Article  CAS  Google Scholar 

  19. Porath I, Fornstedt N. Group fractionation of plasma proteins on dipolar ion exchangers. J Chromatogr A. 1970;51:479–89.

    Article  CAS  Google Scholar 

  20. Zuker M. Mfold web server for nucleic acid folding and hybridization prediction. Nucleic Acids Res. 2003;31:3406–15.

    Article  CAS  Google Scholar 

  21. Mann D, Reinemann C, Stoltenburg R, Strehlitz B. In vitro selection of DNA aptamers binding ethanolamine. Biochem Biophys Res Commun. 2005;338:1928–34.

    Article  CAS  Google Scholar 

  22. Mehta J, Van Dorst B, Rouah-Martin E, Herrebout W, Scippo ML, Blust R, et al. In vitro selection and characterization of DNA aptamers recognizing chloramphenicol. J Biotechnol. 2011;155:361–9.

    Article  CAS  Google Scholar 

  23. Cheng R, Liu S, Shi H, Zhao G. A highly sensitive and selective aptamer-based colorimetric sensor for the rapid detection of PCB 77. J Hazard Mater. 2018;341:373–80.

    Article  Google Scholar 

  24. Harada K, Frankel AD. Identification of two novel arginine binding DNAs. EMBO J. 1995;14:5798–811.

    Article  CAS  Google Scholar 

  25. Paramasivan S, Rujan L, Bolton PH. Circular dichroism of quadruplex DNAs: applications to structure, cation effects and ligand binding. Methods. 2007;43:324–31.

    Article  CAS  Google Scholar 

  26. Chang YM, Chen CK, Hou MH. Conformational changes in DNA upon ligand binding monitored by circular dichroism. Int J Mol Sci. 2012;13:3394–413.

    Article  CAS  Google Scholar 

  27. Xu S, Yuan H, Chen S, Xu A, Wang J, Wu L. Selection of DNA aptamers against polychlorinated biphenyls as potential biorecognition elements for environmental analysis. Anal Biochem. 2012;423:195–201.

    Article  CAS  Google Scholar 

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Acknowledgments

The authors would like to thank Dr. Alan Clark for guidance in the preparation of affinity matrices, Dr. Junsheng Lin for scientific discussions and aid in designing the processes of image capturing and analysing, and Dr. Guozheng Liu for proofreading the manuscript.

Funding

This work was financially supported by the Ministry of Science and Innovation of New Zealand (contract number C08X0708).

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Correspondence to Shiwei Li.

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Li, S., Clarkson, M. & McNatty, K. Selection and characterisation of triclosan-specific aptamers using a fluorescence microscope-imaging assay. Anal Bioanal Chem 412, 7285–7294 (2020). https://doi.org/10.1007/s00216-020-02863-7

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  • DOI: https://doi.org/10.1007/s00216-020-02863-7

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