School of Pharmacy, Nantong University, Nantong, Jiangsu 226001, China.
School of Chemistry and Chemical Engineering, Frontiers Science Center for Transformative Molecules, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai 200240, China.
Lab Chip. 2022 May 31;22(11):2165-2172. doi: 10.1039/d2lc00096b.
Analysis of single-cell microRNA is essential to reveal cell heterogeneity at the genetic level. It raises a high demand for single-cell analytical methods because single-cell microRNA sequences are highly similar and small in size and feature low-level expression. Herein, SERS and fluorescence imaging technology were introduced into a microfluidic droplet platform to realize direct , nondestructive, and highly sensitive detection of a small number of microRNA-21 (miR-21) in a single intact living cell. A multifunctional plasmonic nanoprobe was designed by decorating a gold nanoparticle with fluorescent dye (ROX)-labeled probe DNA and capture DNA strands. The dual-signal switching of fluorescence turn-off and SERS turn-on of ROX in response to miR-21 achieves highly sensitive and reliable detection of miR-21 in a single cell. The turn-on of SERS signal with a zero background guarantees the sensitivity of the detection. The fluorescence-SERS simultaneous response strategy was able to mutually corroborate the test results, improving the reliability of determining low-level expression of miR-21. SERS combined with encapsulation of microdroplets provides a feasible way to conduct , nondestructive determination of miR-21 secreted by single cells, avoiding cell lysis and tedious time-consuming steps of miR-21 isolation. As a result, the miR-21 expressed by various types of single cells was investigated by fluorescence imaging and the cellular heterogeneity in miR-21 expression was evaluated accurately and quantitatively by SERS. This research would provide important reference information for understanding the effects of miRNAs on cancer diseases at the single-cell level.
单细胞 microRNA 分析对于揭示遗传水平上的细胞异质性至关重要。由于单细胞 microRNA 序列高度相似且尺寸小、表达水平低,因此对单细胞分析方法提出了很高的要求。在此,将 SERS 和荧光成像技术引入微流控液滴平台,以实现对单个完整活细胞中少量 microRNA-21(miR-21)的直接、无损和高灵敏度检测。通过将荧光染料(ROX)标记的探针 DNA 和捕获 DNA 链修饰到金纳米颗粒上,设计了多功能等离子体纳米探针。ROX 对 miR-21 的荧光猝灭和 SERS 开启的双信号转换实现了单个细胞中 miR-21 的高灵敏度和可靠检测。SERS 信号的开启具有零背景,保证了检测的灵敏度。荧光-SERS 同时响应策略能够相互佐证测试结果,提高了低水平表达 miR-21 测定的可靠性。SERS 与微液滴封装相结合,为进行单细胞分泌的 miR-21 的无损测定提供了可行的方法,避免了细胞裂解和 miR-21 分离的繁琐耗时步骤。因此,通过荧光成像研究了各种类型的单细胞中表达的 miR-21,并通过 SERS 准确、定量地评估了 miR-21 表达的细胞异质性。该研究将为在单细胞水平上理解 miRNA 对癌症疾病的影响提供重要参考信息。