Single-microbead space-confined digital quantification strategy (SMSDQ) for counting microRNAs at the single-molecule level

微珠(研究) 表面等离子共振 胶体金 纳米技术 化学 费斯特共振能量转移 分析物 材料科学 纳米颗粒 色谱法 荧光 光学 物理 生物化学
作者
Yuanwen Liang,Desheng Chen,Honghong Wang,Hongru Pian,Weiliang Liu,Fangfang Wang,Hui Wang,Zhengping Li
出处
期刊:Biosensors and Bioelectronics [Elsevier BV]
卷期号:238: 115578-115578
标识
DOI:10.1016/j.bios.2023.115578
摘要

Quantification of microRNAs (miRNAs) at the single-molecule level is of great significance for clinical diagnostics and biomedical research. The challenges lie in the limits to transforming single-molecule measurements into quantitative signals. To address these limits, here, we report a new approach called a Single Microbead-based Space-confined Digital Quantification (SMSDQ) to measure individual miRNA molecules by counting gold nanoparticles (AuNPs) with localized surface plasmon resonance (LSPR) light-scattering imaging. One miRNA target hybridizes with the alkynyl-modified capture DNA probe immobilized on a microbead (60 μm) and the azide-modified report DNA probe anchored on AuNP (50 nm), respectively. Through the click reaction between the alkynyl and azide group, a single microbead can covalently link the AuNPs in the confined space within the view of the microscope. By digitally counting the light-scattering spots of AuNPs, we demonstrated the proposed approach with single-molecule detection sensitivity and high specificity of single-base discrimination. Taking the advantages of ultrahigh sensitivity, specificity, and the digital detection manner, the approach is suitable for evaluating cell heterogeneity and small variations of miRNA expression and has been successfully applied to direct quantification of miRNAs in one-tenth single-cell lysates and serum samples without RNA-isolated and nucleic acid amplification steps.
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