Key Laboratory of Applied Surface and Colloid Chemistry, Ministry of Education, Key Laboratory of Analytical Chemistry for Life Science of Shaanxi Province, School of Chemistry & Chemical Engineering, Shaanxi Normal University, Xi'an, 710119, China.
Key Laboratory of Applied Surface and Colloid Chemistry, Ministry of Education, Key Laboratory of Analytical Chemistry for Life Science of Shaanxi Province, School of Chemistry & Chemical Engineering, Shaanxi Normal University, Xi'an, 710119, China.
Biosens Bioelectron. 2024 Oct 1;261:116508. doi: 10.1016/j.bios.2024.116508. Epub 2024 Jun 18.
Digital counting assays, that quantify targets by counting individual signal entities, provide a promising way for the sensitive analysis of biomarkers even at the single-molecule level. Considering the requirements of complex enzyme-catalyzed amplification techniques and specialized instruments in traditional digital counting biosensors, herein, a simple digital counting platform for microRNA (miRNA) analysis is developed by employing the miRNA-templated click chemical ligation to hinge ultrabright quantum dot-doped nanoparticles (QDNPs) on the bottom of microplate well. Compared with the traditional short miRNA-mediated sandwich hybridization mechanism, the click chemistry-mediated ligation featured enhanced stability, achieving higher sensitivity by directly counting the number of QDNPs with a common wide-field fluorescence microscope. Furthermore, enzyme-free cycling click ligation strategy is adopted to push the detection limit of miRNA down to a low level of 8 fM. What is more, taking advantages of the tunable emission wavelength and narrow emission spectra of fluorescent nanoparticles, the platform enables simultaneous detection of multiplex miRNA targets without cross interference. Benefiting from the simple operation, high sensitivity, and good generality, miRNA analysis in complex samples is successfully achieved. This method not only pioneers a new route for digital counting assays but also holds great potential in miRNA-related biological researches.
数字计数分析方法通过逐个计数信号实体来定量目标,即使在单分子水平上也能为生物标志物的敏感分析提供一种很有前途的方法。考虑到传统数字计数生物传感器中复杂酶促扩增技术和专用仪器的要求,本研究通过采用 miRNA 模板点击化学连接将超亮量子点掺杂纳米颗粒(QDNPs)铰链到微孔板底部,开发了一种用于 miRNA 分析的简单数字计数平台。与传统的短 miRNA 介导的三明治杂交机制相比,点击化学介导的连接具有更高的稳定性,通过用普通宽场荧光显微镜直接计数 QDNPs 的数量,实现了更高的灵敏度。此外,采用无酶循环点击连接策略将 miRNA 的检测限推低至 8 fM 的低水平。更重要的是,利用荧光纳米粒子可调发射波长和窄发射光谱的特性,该平台能够实现多重 miRNA 靶标同时检测而不会相互干扰。该平台操作简单、灵敏度高、通用性好,成功实现了复杂样品中的 miRNA 分析。该方法不仅为数字计数分析方法开辟了新途径,而且在 miRNA 相关的生物学研究中也具有很大的潜力。