4.7 Article

Detection of inflammatory bowel disease (IBD)-associated microRNAs by two color DNA-templated silver nanoclusters fluorescent probes

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PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.saa.2022.121185

Keywords

Multiplex miRNAs; DNA-templated silver nanoclusters; Fluorescence probe

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Funding

  1. Natural Science Foundation of Shaanxi Province of China [2020JQ-087]
  2. China Postdoctoral Science Foundation, China [2019M663657]
  3. Zhejiang Provincial Natural Science Foundation of China [LY20H180010]
  4. Founda-tion of Zhejiang Educational Committee [Y202045346]
  5. Wenzhou Science and Technology Bureau [Y20180142]

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Research has shown that circulating miRNAs can be used as novel diagnostic and prognostic markers for patients with inflammatory bowel diseases (IBD). In this study, a fluorescent probe was developed for simultaneous detection of two serum biomarkers (miR-23a and miR-223) associated with ulcerative colitis (UC) activity. The method showed high selectivity and has the potential for clinical application.
Researches demonstrated that circulating miRNAs could be used as novel diagnostic and prognostic potential markers for patients with inflammatory bowel diseases (IBD). It is of great significance in clinical to develop rapid and specific detection methods for miRNAs. Herein, we established a fluorescent probe for ulcerative colitis (UC) activity-associated two serum biomarkers (miR-23a and miR-223) simultaneous detection, which used multi-color fluorescent DNA-stabilized silver nanoclusters (DNA-AgNC) illuminated by a close guanine (G)-rich sequence as a signal transducer and two split DNA probes as recognition units. In principle, the two DNA probe sequences containing AgNC nucleation sequence and G-rich sequence respectively, formed a ternary complex when in the presence of target miRNA through base pairing, so as to induce enhancement of fluorescence emission of AgNC by shortening the distance from G-rich sequence. The combined probes for miR-23a and miR-223 detection generated increased fluorescence signals at 460 nm ex/545 nm em and at 560 nm ex/630 nm em, respectively. With this technique, we successfully quantified the two target miRNAs with high selectivity. Furthermore, the potential clinic applicability of this method was verified by testing the spiked standard miRNAs in human serum. Thus, this one-step, low-cost, and homogenous method offers a great opportunity for disease associated multiplex miRNAs simultaneous detection. (c) 2022 Elsevier B.V. All rights reserved.

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