Plasmonic Molecular Entrapment for Label‐Free Methylated DNA Detection and Machine‐Learning Assisted Quantification

Epigenetic DNA methylations are linked to the activation of oncogenes and inactivation of tumor suppressor genes. A reliable and label-free method to quantitatively measure DNA methylation levels is essential for diagnosing and monitoring methylation-related diseases. Herein, plasmonic molecular entrapment (PME) method assisted SERS as facile strategy for trapping and label-free sensing of DNA methylation, utilizing in situ surface growth of plasmonic particle in the presence of target analytes, are developed. This highly sensitive and adaptable technique forms hotspot sites around target analytes, overcoming mismatch geometrical properties and producing a strong electromagnetic field that leads to significant SERS signal enhancement. The PME method effectively profiles and quantifies DNA methylation, demonstrating robust capabilities for DNA analysis. A logistic regression (LR)-based machine learning accurately quantifies and classifies methylation levels in clinical serum samples of colorectal cancer and normal patients with high sensitivity, specificity, and accuracy, highlighting the feasibility of this technique. The developed PME method combined with machine learning offers promising sensing techniques for disease screening and diagnosis, marking a significant advancement in disease detection and patient care.

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Publication Details

Journal
Advanced Science
Published
2025-05-08
DOI
https://doi.org/10.1002/advs.202503257
Citations
2
Primary Topic
Gold and Silver Nanoparticles Synthesis and Applications
Type
article
Field-Weighted Citation Impact
0.85

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article

Plasmonic Molecular Entrapment for Label‐Free Methylated DNA Detection and Machine‐Learning Assisted Quantification

Muhammad Shalahuddin Al Ja’farawy, Vo Thi Nhat Linh, Ho Sang Jung, Rowoon Park et al.
2 citations
Advanced Science
Gold and Silver Nanoparticles Synthesis and Applications
0.85
article

Plasmonic Molecular Entrapment for Label‐Free Methylated DNA Detection and Machine‐Learning Assisted Quantification

Muhammad Shalahuddin Al Ja’farawy, Vo Thi Nhat Linh, Ho Sang Jung, Rowoon Park, ChaeWon Mun, Sung‐Gyu Park, Jun-Young Yang, Min‐Young Lee, Dongho Kim, Jun Young Kim
article en
2 citations

Abstract

Epigenetic DNA methylations are linked to the activation of oncogenes and inactivation of tumor suppressor genes. A reliable and label-free method to quantitatively measure DNA methylation levels is essential for diagnosing and monitoring methylation-related diseases. Herein, plasmonic molecular entrapment (PME) method assisted SERS as facile strategy for trapping and label-free sensing of DNA methylation, utilizing in situ surface growth of plasmonic particle in the presence of target analytes, are developed. This highly sensitive and adaptable technique forms hotspot sites around target analytes, overcoming mismatch geometrical properties and producing a strong electromagnetic field that leads to significant SERS signal enhancement. The PME method effectively profiles and quantifies DNA methylation, demonstrating robust capabilities for DNA analysis. A logistic regression (LR)-based machine learning accurately quantifies and classifies methylation levels in clinical serum samples of colorectal cancer and normal patients with high sensitivity, specificity, and accuracy, highlighting the feasibility of this technique. The developed PME method combined with machine learning offers promising sensing techniques for disease screening and diagnosis, marking a significant advancement in disease detection and patient care.

Advanced ScienceVol. 12(29)
Pohang University of Science and Technology (KR), Korea Institute of Materials Science (KR), Korea University of Science and Technology (KR)
National Research Foundation, Ministry of Trade, Industry and Energy, Ministry of Science and ICT, South Korea, Korea Evaluation Institute of Industrial Technology, Korea Institute of Materials Science
Openalex Percentile: Top 29%
Gold and Silver Nanoparticles Synthesis and Applications
0.85
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