Iontronic sensor demonstrates simultaneous detection of DNA and RNA modifications, suggesting improved epigenetic analysis capabilities.
DNA and RNA methylations constitute two interconnected regulatory layers of gene expression. Simultaneous detection of DNA 5-methylcytosine (m⁵C-DNA) and RNA N6-methyladenosine (m⁶A-RNA) is essential for capturing multilayer epigenetic and epitranscriptomic information while avoiding the interpretative bias that often arises from single-modification measurements. In this study, we report an iontronic sensing method based on an anodic aluminum oxide (AAO) nanochannel, which can detect both m⁵C-DNA and m⁶A-RNA. The sensor relies on modulation of the ionic current in the confined AAO nanochannel and integrates nucleic acid amplification reactions, including catalytic hairpin assembly, hybridization chain reaction, and double-strand-specific nuclease-assisted amplification strategies to achieve high sensitivity and specificity. The developed sensor exhibited sensitive responses toward m⁵C-DNA and m⁶A-RNA, with detection limits of 1.01 and 1.32 fM, respectively. The platform shows excellent selectivity, repeatability, and long-term stability. Satisfied recoveries obtained in spiked serum samples confirm its strong anti-interference capability, which is suitable for complex biological matrices. Moreover, by introducing a Boolean logic tree framework, the sensor can decode multiple iontronic signals and reduce ambiguity in dual-methylation analysis, which allows for the flexible distinction and analysis of multiple nucleic acid modification events. By integrating high-sensitivity iontronic readout with logic-guided signal interpretation, this work establishes a versatile platform for multitarget epigenetic analysis. The proposed strategy can expand the analytical capability of nanochannel-based iontronic sensors and offer new opportunities for early disease diagnostics and precision medicine applications.
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Tang et al. (2026) studied this question.
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