Label-free detection of DNA methylation by surface-enhanced Raman spectroscopy using zirconium-modified silver nanoparticles

被引:25
作者
Zhang, Yuan [1 ]
Zhan, De-Sheng [1 ]
Xu, Xiao-Ying [2 ]
Zhang, Zhe [2 ]
Hafez, Mahmoud Elsayed [1 ,3 ]
He, Yue [1 ]
Li, Yang [2 ]
Li, Da-Wei [1 ]
机构
[1] East China Univ Sci & Technol, Frontiers Sci Ctr Materiobiol & Dynam Chem, Sch Chem & Mol Engn, Key Lab Adv Mat,Joint Int Lab Precis Chem,Shanghai, Shanghai 200237, Peoples R China
[2] Harbin Med Univ, Coll Pharm, Res Ctr Innovat Technol Pharmaceut Anal, Dept Pharmaceut Anal & Analyt Chem, 157 Baojian Rd, Harbin 150081, Heilongjiang, Peoples R China
[3] Beni Suef Univ, Fac Sci, Dept Chem, Bani Suwayf 62511, Egypt
基金
中国国家自然科学基金;
关键词
Surface -enhanced Raman scattering; Zirconium ions; Single -base detection; DNA methylation Detection; SINGLE; DAMAGE; AG;
D O I
10.1016/j.talanta.2022.123941
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
DNA methylation is an important feature of gene epigenetics that affects the metabolic process of organisms. Although surface-enhanced Raman spectroscopy (SERS) has demonstrated great potential in label-free DNA detection, discriminating the various processes involved in DNA methylation remains a challenge. DNA mole-cules fold themselves, wrapping the hydrophobic bases, thus making it difficult for traditional methods to detect single-base signals. In this study, we develop a SERS platform for detecting DNA via modifying silver nano -particles by zirconium ions to obtain the DNA fingerprint information of base methylations (N6-methylated adenine and 5-methylated cytosine). Zirconium ions open the folded DNA molecules, enabling SERS signals of the four DNA bases (A, C, G, T) to be obtained as well as identification of the subtle differences between normal and methylated DNA with single base-level sensitivity. Moreover, the identifying information of DNA methyl-ation was obtained by combining principal component analysis (PCA) with 2D correlation spectroscopy analysis. The findings of this study provide a substantial progress for current platforms for DNA sequencing, genetic testing, and gene-disease treatment.
引用
收藏
页数:8
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