光漂白
量子点
环介导等温扩增
材料科学
荧光团
荧光
检出限
胺气处理
寡核苷酸
光致发光
核酸
纳米探针
光化学
组合化学
分析化学(期刊)
纳米技术
化学
纳米颗粒
光电子学
色谱法
有机化学
DNA
生物化学
物理
量子力学
作者
Shiyao Wang,Ailin Qin,Li Yin Chau,Eunice W. T. Fok,Mei Yue Choy,Christopher J. Brackman,G. G. Siu,Chien‐Ling Huang,Shea Ping Yip,Thomas M. H. Lee
标识
DOI:10.1021/acsami.2c02508
摘要
Loop-mediated isothermal amplification (LAMP) has received considerable attention for decentralized (point-of-care and on-site) nucleic acid testing in view of its simple temperature control (60-65 °C) and short assay time (15-60 min). There remains a challenge in its wide adoption and acceptance due to the limitations of the existing amplification result reporter probes, e.g., photobleaching of organic fluorophore and reduced sensitivity of the pH-sensitive colorimetric dye. Herein, we demonstrate CdSeS/ZnS quantum dots (semiconductor fluorescent nanocrystals with superior photostability than organic fluorophore) with surface modification of cysteamine (amine-QDs) as a new reporter probe for LAMP that enabled single-copy sensitivity (limit of detection of 83 zM; 20 μL reaction volume). For a negative LAMP sample (absence of target sequence), positively charged amine-QDs remained dispersed due to interparticle electrostatic repulsion. While for a positive LAMP sample (presence of target sequence), amine-QDs became precipitated. The characterization data showed that amine-QDs were embedded in magnesium pyrophosphate crystals (generated during positive LAMP), thus leading to their coprecipitation. This amine-QD-based one-step LAMP assay advances the field of QD-based nucleic acid amplification assays in two aspects: (1) compatibility─one-step amplification and detection (versus separation of amplification and detection steps); and (2) universality─the same amine-QDs for different target sequences (versus different oligonucleotide-modified QDs for different target sequences).
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