Enzyme-free sensitive SERS biosensor for the detection of thalassemia-associated microRNA-210 using a cascade dual-signal amplification strategy

• Published in: Analytica chimica acta Vol. 1292; p. 342255
• Main Authors: Chen, Qiying, Chen, Huagan, Kong, Hongxing, Chen, Ruijue, Gao, Si, Wang, Ying, Zhou, Pei, Huang, Wenyi, Cheng, Hao, Li, Lijun, Feng, Jun
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01.03.2024
• Subjects: beta-Thalassemia - diagnosis; beta-Thalassemia - genetics; Biosensing Techniques - methods; Catalytic hairpin assembly reaction (CHA); DNA; gamma-Globins; Gold; Humans; Hybridization chain reaction (HCR); Limit of Detection; Metal Nanoparticles; MicroRNA-210 (miR-210); MicroRNAs; Spectrum Analysis, Raman; Surface-enhanced Raman scattering (SERS); β-thalassemia; Catalytic hairpin assembly reaction (CHA); Surface-enhanced Raman scattering (SERS); MicroRNA-210 (miR-210); β-thalassemia; Hybridization chain reaction (HCR)
• ISSN: 0003-2670; 1873-4324
• DOI: 10.1016/j.aca.2024.342255

β-thalassemia is a blood disorder caused by autosomal mutations. Gene modulation therapy to activate the γ-globin gene to induce fetal hemoglobin (HbF) synthesis has become a new option for the treatment of β-thalassemia. MicroRNA-210 (miR-210) contributes to studying the mechanism regulating γ-globin gene expression and is a potential biomarker for rapid β-thalassemia screening. Traditional miRNA detection methods perform well but necessitate complex and time-consuming miRNA sample processing. Therefore, the development of a sensitive, accurate, and simple miRNA level monitoring method is essential. We have developed a non-enzymatic surface-enhanced Raman scattering (SERS) biosensor utilizing a signal cascade amplification of catalytic hairpin assembly reaction (CHA) and proximity hybridization-induced hybridization chain reaction (HCR). Au@Ag NPs were used as the SERS substrate, and methylene blue (MB)- modified DNA hairpins were used as the SERS tags. The SERS assay involved two stages: implementing the CHA-HCR cascade signal amplification strategy and conducting SERS measurements on the resulting product. The HCR was started by the products of target-triggered CHA, which formed lengthy nicked double-stranded DNA (dsDNA) on the Au@Ag NPs surface to which numerous SERS tags were attached, leading to a significant increase in the SERS signal intensity. High specificity and sensitivity for miR-210 detection was achieved by monitoring MB SERS intensity changes. The suggested SERS biosensor has a low detection limit of 5.13 fM and is capable of detecting miR-210 at concentration between 10 fM and 1.0 nM. The biosensor can detect miR-210 levels in the erythrocytes of β-thalassemia patients, enabling rapid screening for β-thalassemia and suggesting a novel approach for investigating the regulation mechanism of miR-210 on γ-globin gene expression. In the meantime, this innovative technique has the potential to detect additional miRNAs and to become an important tool for the early diagnosis of diseases and for biomedical research. [Display omitted] •We demonstrate a SERS biosensor based on CHA-HCR signaling cascade amplification.•The SERS biosensor can be used to detect miR-210 in β-thalassemia erythrocytes.•The SERS biosensor demonstrated excellent selectivity and remarkable sensitivity.•The detection limit of miR-210 was as low as 5.13 fM.